PUBLICACIÓN

Stereochemical Terminology in Chiral Drugs: Still Between Confusion and Misinterpretation

ACCEDER A LA PUBLICACIÓN: Orcid Dehesa Repositorio Institucional

Juan García de la Concepción; Anthony J. Burke; Pedro Cintas

2026 ACS Medicinal Chemistry Letters

DOI

10.1021/acsmedchemlett.6c00195

AUTORES DE LA UEX

Pedro Cintas Moreno
Juan García De La Concepción

OTRAS PUBLICACIONES DE INTERÉS

Síntesis De Hidrobromuros De Glucopirano [2,1-D]-2-Tiazolinas
Beyond Conglomerates: A Minimalist Model Of The Viedma Deracemization Of Dl-Amino Acids
Graphene Oxide–enamino-Xanthene Charge-Transfer Hybrids As High-Performance Sensitizing Interfaces For Tio2photoanodes
Beyond Conglomerates: A Minimalist Model Of The Viedma Deracemization Of Dl-Amino Acids
Graphene Oxide–enamino-Xanthene Charge-Transfer Hybrids As High-Performance Sensitizing Interfaces For Tio2photoanodes
Memantine: A Look Ahead. Insights Into Structure, Syntheses, Receptor Binding Mechanisms, Drug Hybrids And Formulations, And Potential Repurposing
Graphene Oxide–enamino-Xanthene Charge-Transfer Hybrids As High-Performance Sensitizing Interfaces For Tio2photoanodes
Memantine: A Look Ahead. Insights Into Structure, Syntheses, Receptor Binding Mechanisms, Drug Hybrids And Formulations, And Potential Repurposing
Expanding The Chemical Space Of D-Mannosamine Imines – A Combined Experimental And Computational Analysis Of Anomeric And Tautomeric Equilibria
Memantine: A Look Ahead. Insights Into Structure, Syntheses, Receptor Binding Mechanisms, Drug Hybrids And Formulations, And Potential Repurposing
Expanding The Chemical Space Of D-Mannosamine Imines – A Combined Experimental And Computational Analysis Of Anomeric And Tautomeric Equilibria
Stereochemical Terminology In Chiral Drugs: Still Between Confusion And Misinterpretation
Expanding The Chemical Space Of D-Mannosamine Imines – A Combined Experimental And Computational Analysis Of Anomeric And Tautomeric Equilibria
Stereochemical Terminology In Chiral Drugs: Still Between Confusion And Misinterpretation
Unraveling The Conglomeratic Nature Of Methanol Clusters Adsorbed On Graphene Surfaces. Insights From Molecular Dynamics Simulations
Stereochemical Terminology In Chiral Drugs: Still Between Confusion And Misinterpretation
Unraveling The Conglomeratic Nature Of Methanol Clusters Adsorbed On Graphene Surfaces. Insights From Molecular Dynamics Simulations
Catalytic Screening For 1,2-Diol Protection: A Saccharose-Derived Hydrothermal Carbon Showcases Enhanced Performance
Unraveling The Conglomeratic Nature Of Methanol Clusters Adsorbed On Graphene Surfaces. Insights From Molecular Dynamics Simulations
Catalytic Screening For 1,2-Diol Protection: A Saccharose-Derived Hydrothermal Carbon Showcases Enhanced Performance
Targeting Cow's Milk Allergy Using Hypoallergenic Protein-Polyphenol Formulas: A Proof Of Concept
Catalytic Screening For 1,2-Diol Protection: A Saccharose-Derived Hydrothermal Carbon Showcases Enhanced Performance
Targeting Cow's Milk Allergy Using Hypoallergenic Protein-Polyphenol Formulas: A Proof Of Concept
150 Years Of The Tetrahedral Carbon: A Toast To Chirality
Targeting Cow's Milk Allergy Using Hypoallergenic Protein-Polyphenol Formulas: A Proof Of Concept
150 Years Of The Tetrahedral Carbon: A Toast To Chirality
Novel Graphitic Oxynitrides As Photocatalysts For Sustainable H2 Production And Co2 Valorization. The Importance Of Self-Assembly For Catalytic Activity
150 Years Of The Tetrahedral Carbon: A Toast To Chirality
Novel Graphitic Oxynitrides As Photocatalysts For Sustainable H2 Production And Co2 Valorization. The Importance Of Self-Assembly For Catalytic Activity
Tuning Synthesis And Sonochemistry Forges Learning And Enhances Educational Training: Protection Of 1,3-Diols Under Heterogeneous Catalysis As Sustainable Case Study
Novel Graphitic Oxynitrides As Photocatalysts For Sustainable H2 Production And Co2 Valorization. The Importance Of Self-Assembly For Catalytic Activity
Tuning Synthesis And Sonochemistry Forges Learning And Enhances Educational Training: Protection Of 1,3-Diols Under Heterogeneous Catalysis As Sustainable Case Study
Catalytic Innovations In The Aza-Michael Reaction: An Experimental Benchmarking Focused On Sustainable Approaches
Tuning Synthesis And Sonochemistry Forges Learning And Enhances Educational Training: Protection Of 1,3-Diols Under Heterogeneous Catalysis As Sustainable Case Study
Catalytic Innovations In The Aza-Michael Reaction: An Experimental Benchmarking Focused On Sustainable Approaches
Understanding Bio-Orthogonal Strain-Driven Sydnone Cycloadditions: Data-Assisted Profiles And The Search For Linear Relationships
Catalytic Innovations In The Aza-Michael Reaction: An Experimental Benchmarking Focused On Sustainable Approaches
Understanding Bio-Orthogonal Strain-Driven Sydnone Cycloadditions: Data-Assisted Profiles And The Search For Linear Relationships
Formic Acid Isomerism In Dark Clouds
Understanding Bio-Orthogonal Strain-Driven Sydnone Cycloadditions: Data-Assisted Profiles And The Search For Linear Relationships
Formic Acid Isomerism In Dark Clouds
Graphene Oxide–enamino-Xanthene Charge-Transfer Hybrids As High-Performance Sensitizing Interfaces For Tio2 Photoanodes
Formic Acid Isomerism In Dark Clouds
Graphene Oxide–enamino-Xanthene Charge-Transfer Hybrids As High-Performance Sensitizing Interfaces For Tio2 Photoanodes
Reverse Anomeric Effects In Pyranose And Furanose Isomers In Schiff Bases Of D-Galactosamine
Graphene Oxide–enamino-Xanthene Charge-Transfer Hybrids As High-Performance Sensitizing Interfaces For Tio2 Photoanodes
Reverse Anomeric Effects In Pyranose And Furanose Isomers In Schiff Bases Of D-Galactosamine
Basic Concepts Of Orbital Theory In Organic Chemistry, Eusebio Juaristi, C. Gabriela Ávila-Ortiz Y Alberto Vega-Peñaloza
Reverse Anomeric Effects In Pyranose And Furanose Isomers In Schiff Bases Of D-Galactosamine
Basic Concepts Of Orbital Theory In Organic Chemistry, Eusebio Juaristi, C. Gabriela Ávila-Ortiz Y Alberto Vega-Peñaloza
Sonochemical Activation In Flow Systems
Basic Concepts Of Orbital Theory In Organic Chemistry, Eusebio Juaristi, C. Gabriela Ávila-Ortiz Y Alberto Vega-Peñaloza
Sonochemical Activation In Flow Systems
Relevance Of The P+o2 Reaction For Po Formation In Astrochemical Environments: Electronic Structure Calculations And Kinetic Simulations
Sonochemical Activation In Flow Systems
Relevance Of The P+o2 Reaction For Po Formation In Astrochemical Environments: Electronic Structure Calculations And Kinetic Simulations
From Potential Prebiotic Synthons To Useful Chiral Scaffolds: A Synthetic And Structural Reinvestigation Of 2-Amino-Aldononitriles
Relevance Of The P+o2 Reaction For Po Formation In Astrochemical Environments: Electronic Structure Calculations And Kinetic Simulations
From Potential Prebiotic Synthons To Useful Chiral Scaffolds: A Synthetic And Structural Reinvestigation Of 2-Amino-Aldononitriles
A True Reverse Anomeric Effect Does Exist After All: A Hydrogen Bonding Stereocontrolling Effect In 2-Iminoaldoses
From Potential Prebiotic Synthons To Useful Chiral Scaffolds: A Synthetic And Structural Reinvestigation Of 2-Amino-Aldononitriles
A True Reverse Anomeric Effect Does Exist After All: A Hydrogen Bonding Stereocontrolling Effect In 2-Iminoaldoses
Norcaradiene-Cycloheptatriene Equilibrium: A Heavy-Atom Quantum Tunneling Case
A True Reverse Anomeric Effect Does Exist After All: A Hydrogen Bonding Stereocontrolling Effect In 2-Iminoaldoses
Norcaradiene-Cycloheptatriene Equilibrium: A Heavy-Atom Quantum Tunneling Case
Preparación De Carbamatos A Partir De Aminas Aromáticas Mediante Catálisis Heterogénea
Norcaradiene-Cycloheptatriene Equilibrium: A Heavy-Atom Quantum Tunneling Case
Preparación De Carbamatos A Partir De Aminas Aromáticas Mediante Catálisis Heterogénea
Exploring And Re-Assessing Reverse Anomeric Effect In 2-Iminoaldoses Derived From Mono- And Polynuclear Aromatic Aldehydes
Preparación De Carbamatos A Partir De Aminas Aromáticas Mediante Catálisis Heterogénea
Exploring And Re-Assessing Reverse Anomeric Effect In 2-Iminoaldoses Derived From Mono- And Polynuclear Aromatic Aldehydes
Unfruitful Chemical Pathway For Interstellar Furan: Formation Of The Four Isomers Of 1-Butenol-3-Yne
Exploring And Re-Assessing Reverse Anomeric Effect In 2-Iminoaldoses Derived From Mono- And Polynuclear Aromatic Aldehydes
Unfruitful Chemical Pathway For Interstellar Furan: Formation Of The Four Isomers Of 1-Butenol-3-Yne
First Detection In Space Of The High-Energy Isomer Of Cyanomethanimine: H2cncn
Unfruitful Chemical Pathway For Interstellar Furan: Formation Of The Four Isomers Of 1-Butenol-3-Yne
First Detection In Space Of The High-Energy Isomer Of Cyanomethanimine: H2cncn
Antioxidant Activity And Hypoallergenicity Of Egg Protein Matrices Containing Polyphenols From Citrus Waste
First Detection In Space Of The High-Energy Isomer Of Cyanomethanimine: H2cncn
Antioxidant Activity And Hypoallergenicity Of Egg Protein Matrices Containing Polyphenols From Citrus Waste
Síntesis De Acetales Derivados De 1,2-Dioles En Presencia De Catalizadores Ácidos Carbonosos
Antioxidant Activity And Hypoallergenicity Of Egg Protein Matrices Containing Polyphenols From Citrus Waste
Síntesis De Acetales Derivados De 1,2-Dioles En Presencia De Catalizadores Ácidos Carbonosos
Bifunctional Azido(Thio)ureas From An O-Protected 2-Amino-2-Deoxy-D-Glucopyranose: Synthesis And Structural Analyses
Síntesis De Acetales Derivados De 1,2-Dioles En Presencia De Catalizadores Ácidos Carbonosos
Bifunctional Azido(Thio)ureas From An O-Protected 2-Amino-2-Deoxy-D-Glucopyranose: Synthesis And Structural Analyses
Ultrasound And Sonochemistry Enhance Education Outcomes: From Fundamentals And Applied Research To Entrepreneurial Potential
Bifunctional Azido(Thio)ureas From An O-Protected 2-Amino-2-Deoxy-D-Glucopyranose: Synthesis And Structural Analyses
Ultrasound And Sonochemistry Enhance Education Outcomes: From Fundamentals And Applied Research To Entrepreneurial Potential
Reinvigorating Aza-Michael Reactions Under Ionic Liquid Catalysis: A Greener Approach†
Ultrasound And Sonochemistry Enhance Education Outcomes: From Fundamentals And Applied Research To Entrepreneurial Potential
Reinvigorating Aza-Michael Reactions Under Ionic Liquid Catalysis: A Greener Approach†
An Eco-Friendly And Switchable Carbon-Based Catalyst For Protection-Deprotection Of Vicinal Diols
Reinvigorating Aza-Michael Reactions Under Ionic Liquid Catalysis: A Greener Approach†
An Eco-Friendly And Switchable Carbon-Based Catalyst For Protection-Deprotection Of Vicinal Diols
Revisiting Homochiral Versus Heterochiral Interactions Through A Long Detective Story Of A Useful Azobis-Nitrile And Puzzling Racemate
An Eco-Friendly And Switchable Carbon-Based Catalyst For Protection-Deprotection Of Vicinal Diols
Revisiting Homochiral Versus Heterochiral Interactions Through A Long Detective Story Of A Useful Azobis-Nitrile And Puzzling Racemate
A Sequential Acid-Base Mechanism In The Interstellar Medium: The Emergence Of Cis-Formic Acid In Dark Molecular Clouds
Revisiting Homochiral Versus Heterochiral Interactions Through A Long Detective Story Of A Useful Azobis-Nitrile And Puzzling Racemate
A Sequential Acid-Base Mechanism In The Interstellar Medium: The Emergence Of Cis-Formic Acid In Dark Molecular Clouds
Food Allergens: When Friends Become Foes—caveats And Opportunities For Oral Immunotherapy Based On Deactivation Methods
A Sequential Acid-Base Mechanism In The Interstellar Medium: The Emergence Of Cis-Formic Acid In Dark Molecular Clouds
Food Allergens: When Friends Become Foes—caveats And Opportunities For Oral Immunotherapy Based On Deactivation Methods
A New Series Of Acylhydrazones Derived From Metribuzin With Modulated Herbicidal Activity
Food Allergens: When Friends Become Foes—caveats And Opportunities For Oral Immunotherapy Based On Deactivation Methods
A New Series Of Acylhydrazones Derived From Metribuzin With Modulated Herbicidal Activity
Paving The Way To The Synthesis Of Pahs In Dark Molecular Clouds: The Formation Of Cyclopentadienyl Radical (C-C5h5)
A New Series Of Acylhydrazones Derived From Metribuzin With Modulated Herbicidal Activity
Paving The Way To The Synthesis Of Pahs In Dark Molecular Clouds: The Formation Of Cyclopentadienyl Radical (C-C5h5)
H2cn/h2nc Abundance Ratio: A New Potential Temperature Tracer For The Interstellar Medium
Paving The Way To The Synthesis Of Pahs In Dark Molecular Clouds: The Formation Of Cyclopentadienyl Radical (C-C5h5)
H2cn/h2nc Abundance Ratio: A New Potential Temperature Tracer For The Interstellar Medium
Mechanistic Insights Into The Oxidative Degradation Of Formic And Oxalic Acids With Ozone And Oh Radical. A Computational Rationale
H2cn/h2nc Abundance Ratio: A New Potential Temperature Tracer For The Interstellar Medium
Mechanistic Insights Into The Oxidative Degradation Of Formic And Oxalic Acids With Ozone And Oh Radical. A Computational Rationale
Schiff Bases And Stereocontrolled Formation Of Fused 1,3-Oxazolidines From 1-Amino-2-Indanol: A Systematic Study On Structure And Mechanism
Mechanistic Insights Into The Oxidative Degradation Of Formic And Oxalic Acids With Ozone And Oh Radical. A Computational Rationale
Schiff Bases And Stereocontrolled Formation Of Fused 1,3-Oxazolidines From 1-Amino-2-Indanol: A Systematic Study On Structure And Mechanism
The Trans/cis Ratio Of Formic (Hcooh) And Thioformic (Hc(O)sh) Acids In The Interstellar Medium
Schiff Bases And Stereocontrolled Formation Of Fused 1,3-Oxazolidines From 1-Amino-2-Indanol: A Systematic Study On Structure And Mechanism
The Trans/cis Ratio Of Formic (Hcooh) And Thioformic (Hc(O)sh) Acids In The Interstellar Medium
Process Intensification In Continuous Flow Organic Synthesis With Enabling And Hybrid Technologies
The Trans/cis Ratio Of Formic (Hcooh) And Thioformic (Hc(O)sh) Acids In The Interstellar Medium
Process Intensification In Continuous Flow Organic Synthesis With Enabling And Hybrid Technologies
Exophot: The Photon Absorption Rate As A New Metric For Quantifying The Exoplanetary Photosynthetic Activity Fitness
Process Intensification In Continuous Flow Organic Synthesis With Enabling And Hybrid Technologies
Exophot: The Photon Absorption Rate As A New Metric For Quantifying The Exoplanetary Photosynthetic Activity Fitness
The Reactivity Of Pyridine In Cold Interstellar Environments: The Reaction Of Pyridine With The Cn Radical
Exophot: The Photon Absorption Rate As A New Metric For Quantifying The Exoplanetary Photosynthetic Activity Fitness
The Reactivity Of Pyridine In Cold Interstellar Environments: The Reaction Of Pyridine With The Cn Radical
Molecular Precursors Of The Rna-World In Space: New Nitriles In The G+0.693−0.027 Molecular Cloud
The Reactivity Of Pyridine In Cold Interstellar Environments: The Reaction Of Pyridine With The Cn Radical
Molecular Precursors Of The Rna-World In Space: New Nitriles In The G+0.693−0.027 Molecular Cloud
Hydrogen Abstraction Reactions In Formic And Thioformic Acid Isomers By Hydrogen And Deuterium Atoms
Molecular Precursors Of The Rna-World In Space: New Nitriles In The G+0.693−0.027 Molecular Cloud
Hydrogen Abstraction Reactions In Formic And Thioformic Acid Isomers By Hydrogen And Deuterium Atoms
Phot0, A Plausible Primeval Pigment On Earth And Rocky Exoplanets
Hydrogen Abstraction Reactions In Formic And Thioformic Acid Isomers By Hydrogen And Deuterium Atoms
Phot0, A Plausible Primeval Pigment On Earth And Rocky Exoplanets
Ionize Hard: Interstellar Po+ Detection
Phot0, A Plausible Primeval Pigment On Earth And Rocky Exoplanets
Ionize Hard: Interstellar Po+ Detection
Precursors Of The Rna World In Space: Detection Of ( Z)-1,2-Ethenediol In The Interstellar Medium, A Key Intermediate In Sugar Formation
Ionize Hard: Interstellar Po+ Detection
Precursors Of The Rna World In Space: Detection Of ( Z)-1,2-Ethenediol In The Interstellar Medium, A Key Intermediate In Sugar Formation
A Synthetically Benign One-Pot Construction Of Enamino-Xanthene Dyes
Precursors Of The Rna World In Space: Detection Of ( Z)-1,2-Ethenediol In The Interstellar Medium, A Key Intermediate In Sugar Formation
A Synthetically Benign One-Pot Construction Of Enamino-Xanthene Dyes
Switchable Cycloadditions Of Mesoionic Dipoles: Refreshing Up A Regioselective Approach To Two Distinctive Heterocycles
A Synthetically Benign One-Pot Construction Of Enamino-Xanthene Dyes
Switchable Cycloadditions Of Mesoionic Dipoles: Refreshing Up A Regioselective Approach To Two Distinctive Heterocycles
On The Origin Of Sugar Handedness: Facts, Hypotheses And Missing Links-A Review
Switchable Cycloadditions Of Mesoionic Dipoles: Refreshing Up A Regioselective Approach To Two Distinctive Heterocycles
On The Origin Of Sugar Handedness: Facts, Hypotheses And Missing Links-A Review
On An Intensification Factor For Green Chemistry And Engineering: The Value Of An Operationally Simple Decision-Making Tool In Process Assessment
On The Origin Of Sugar Handedness: Facts, Hypotheses And Missing Links-A Review
On An Intensification Factor For Green Chemistry And Engineering: The Value Of An Operationally Simple Decision-Making Tool In Process Assessment
Special Issue On “ultrasound Hybridized Technologies: A New Breathing For Sonochemistry”
On An Intensification Factor For Green Chemistry And Engineering: The Value Of An Operationally Simple Decision-Making Tool In Process Assessment
Special Issue On “ultrasound Hybridized Technologies: A New Breathing For Sonochemistry”
Synthesis Of C: X Ny -Rich Polycyclic Oligomers From Primeval Monomers In Aqueous Media
Special Issue On “ultrasound Hybridized Technologies: A New Breathing For Sonochemistry”
Synthesis Of C: X Ny -Rich Polycyclic Oligomers From Primeval Monomers In Aqueous Media
The Origin Of The E/z Isomer Ratio Of Imines In The Interstellar Medium
Synthesis Of C: X Ny -Rich Polycyclic Oligomers From Primeval Monomers In Aqueous Media
The Origin Of The E/z Isomer Ratio Of Imines In The Interstellar Medium
Diastereoselective Formation Of Trans-Hc(O)sh Through Hydrogenation Of Ocs On Interstellar Dust Grains
The Origin Of The E/z Isomer Ratio Of Imines In The Interstellar Medium
Diastereoselective Formation Of Trans-Hc(O)sh Through Hydrogenation Of Ocs On Interstellar Dust Grains
Formation Of Phosphorus Monoxide (Po) In The Interstellar Medium: Insights From Quantum-Chemical And Kinetic Calculations
Diastereoselective Formation Of Trans-Hc(O)sh Through Hydrogenation Of Ocs On Interstellar Dust Grains
Formation Of Phosphorus Monoxide (Po) In The Interstellar Medium: Insights From Quantum-Chemical And Kinetic Calculations
Detection Of The Cyanomidyl Radical (Hncn): A New Interstellar Species With The Ncn Backbone
Formation Of Phosphorus Monoxide (Po) In The Interstellar Medium: Insights From Quantum-Chemical And Kinetic Calculations
Detection Of The Cyanomidyl Radical (Hncn): A New Interstellar Species With The Ncn Backbone
Organic Sonochemistry: A Chemist's Timely Perspective On Mechanisms And Reactivity
Detection Of The Cyanomidyl Radical (Hncn): A New Interstellar Species With The Ncn Backbone
Organic Sonochemistry: A Chemist's Timely Perspective On Mechanisms And Reactivity
On The Anomeric Preference Of The Isothiocyanato Group
Organic Sonochemistry: A Chemist's Timely Perspective On Mechanisms And Reactivity
On The Anomeric Preference Of The Isothiocyanato Group
Expanding Amphiphilic Architectures By Ring-Opening Of Epoxides And Polyepoxides With N-Methyl-D-Glucamine: Structure, Chiral Bias And Gelation
On The Anomeric Preference Of The Isothiocyanato Group
Expanding Amphiphilic Architectures By Ring-Opening Of Epoxides And Polyepoxides With N-Methyl-D-Glucamine: Structure, Chiral Bias And Gelation
Amphipathic 1,3-Oxazolidines From: N-Alkyl Glucamines And Benzaldehydes: Stereochemical And Mechanistic Studies
Expanding Amphiphilic Architectures By Ring-Opening Of Epoxides And Polyepoxides With N-Methyl-D-Glucamine: Structure, Chiral Bias And Gelation
Amphipathic 1,3-Oxazolidines From: N-Alkyl Glucamines And Benzaldehydes: Stereochemical And Mechanistic Studies
Primo Levi: A Frustrated Stereochemist?—insight In Hindsight
Amphipathic 1,3-Oxazolidines From: N-Alkyl Glucamines And Benzaldehydes: Stereochemical And Mechanistic Studies
Primo Levi: A Frustrated Stereochemist?—insight In Hindsight
Comments On “molecular Chirality In Classical Spacetime: Solving The Controversy About The Spinning Cone Model Of Rotating Molecules”
Primo Levi: A Frustrated Stereochemist?—insight In Hindsight
Comments On “molecular Chirality In Classical Spacetime: Solving The Controversy About The Spinning Cone Model Of Rotating Molecules”
Chasing Synthetic Life: A Tale Of Forms, Chemical Fossils, And Biomorphs
Comments On “molecular Chirality In Classical Spacetime: Solving The Controversy About The Spinning Cone Model Of Rotating Molecules”
Chasing Synthetic Life: A Tale Of Forms, Chemical Fossils, And Biomorphs
A Fully Diastereoselective Oxidation Of A Mesoionic Dipole With Triplet Molecular Oxygen
Chasing Synthetic Life: A Tale Of Forms, Chemical Fossils, And Biomorphs
A Fully Diastereoselective Oxidation Of A Mesoionic Dipole With Triplet Molecular Oxygen
Thermal And Photochemical Switching Of Chiral Sugar Azoalkenes: A Mechanistic Interrogation
A Fully Diastereoselective Oxidation Of A Mesoionic Dipole With Triplet Molecular Oxygen
Thermal And Photochemical Switching Of Chiral Sugar Azoalkenes: A Mechanistic Interrogation
Chasing Synthetic Life: A Tale Of Forms, Chemical Fossils, And Biomorphs
Thermal And Photochemical Switching Of Chiral Sugar Azoalkenes: A Mechanistic Interrogation
Chasing Synthetic Life: A Tale Of Forms, Chemical Fossils, And Biomorphs
Imine Or Enamine? Insights And Predictive Guidelines From The Electronic Effect Of Substituents In H-Bonded Salicylimines
Chasing Synthetic Life: A Tale Of Forms, Chemical Fossils, And Biomorphs
Imine Or Enamine? Insights And Predictive Guidelines From The Electronic Effect Of Substituents In H-Bonded Salicylimines
Pasteur Made Simple-Mechanochemical Transformation Of Racemic Amino Acid Crystals Into Racemic Conglomerate Crystals
Imine Or Enamine? Insights And Predictive Guidelines From The Electronic Effect Of Substituents In H-Bonded Salicylimines
Pasteur Made Simple-Mechanochemical Transformation Of Racemic Amino Acid Crystals Into Racemic Conglomerate Crystals
Does Pressure Break Mirror-Image Symmetry? A Perspective And New Insights
Pasteur Made Simple-Mechanochemical Transformation Of Racemic Amino Acid Crystals Into Racemic Conglomerate Crystals
Does Pressure Break Mirror-Image Symmetry? A Perspective And New Insights
Mutarotation Of Aldoses: Getting A Deeper Knowledge Of A Classic Equilibrium Enabled By Computational Analyses
Does Pressure Break Mirror-Image Symmetry? A Perspective And New Insights
Mutarotation Of Aldoses: Getting A Deeper Knowledge Of A Classic Equilibrium Enabled By Computational Analyses
Alternative Reaction Conditions: Enabling Technologies In Solvent-Free Protocols
Mutarotation Of Aldoses: Getting A Deeper Knowledge Of A Classic Equilibrium Enabled By Computational Analyses
Alternative Reaction Conditions: Enabling Technologies In Solvent-Free Protocols
Interactions Of Amino Acids And Aminoxazole Derivatives: Cocrystal Formation And Prebiotic Implications Enabled By Computational Analysis
Alternative Reaction Conditions: Enabling Technologies In Solvent-Free Protocols
Interactions Of Amino Acids And Aminoxazole Derivatives: Cocrystal Formation And Prebiotic Implications Enabled By Computational Analysis
Electronic Effects In Tautomeric Equilibria: The Case Of Chiral Imines From D-Glucamine And 2-Hydroxyacetophenones
Interactions Of Amino Acids And Aminoxazole Derivatives: Cocrystal Formation And Prebiotic Implications Enabled By Computational Analysis
Electronic Effects In Tautomeric Equilibria: The Case Of Chiral Imines From D-Glucamine And 2-Hydroxyacetophenones
Formation Of: S -Alkyl Thiophenium Ionic Liquids: Mechanistic Rationale And Structural Relationships
Electronic Effects In Tautomeric Equilibria: The Case Of Chiral Imines From D-Glucamine And 2-Hydroxyacetophenones
Formation Of: S -Alkyl Thiophenium Ionic Liquids: Mechanistic Rationale And Structural Relationships
Tautomerism And Stereodynamics In Schiff Bases From Gossypol And Hemigossypol With: N-Aminoheterocycles
Formation Of: S -Alkyl Thiophenium Ionic Liquids: Mechanistic Rationale And Structural Relationships
Tautomerism And Stereodynamics In Schiff Bases From Gossypol And Hemigossypol With: N-Aminoheterocycles
From Prebiotic Chemistry To Supramolecular Oligomers: Urea-Glyoxal Reactions
Tautomerism And Stereodynamics In Schiff Bases From Gossypol And Hemigossypol With: N-Aminoheterocycles
From Prebiotic Chemistry To Supramolecular Oligomers: Urea-Glyoxal Reactions
Cork Wastewater Purification In A Cooperative Flocculation/adsorption Process With Microwave-Regenerated Activated Carbon
From Prebiotic Chemistry To Supramolecular Oligomers: Urea-Glyoxal Reactions
Cork Wastewater Purification In A Cooperative Flocculation/adsorption Process With Microwave-Regenerated Activated Carbon
Computational Screening Of New Orthogonal Metal-Free Dipolar Cycloadditions Of Mesomeric Betaines
Cork Wastewater Purification In A Cooperative Flocculation/adsorption Process With Microwave-Regenerated Activated Carbon
Computational Screening Of New Orthogonal Metal-Free Dipolar Cycloadditions Of Mesomeric Betaines
On The Asymmetric Autocatalysis Of Aldol Reactions: The Case Of 4-Nitrobenzaldehyde And Acetone. A Critical Appraisal With A Focus On Theory
Computational Screening Of New Orthogonal Metal-Free Dipolar Cycloadditions Of Mesomeric Betaines
On The Asymmetric Autocatalysis Of Aldol Reactions: The Case Of 4-Nitrobenzaldehyde And Acetone. A Critical Appraisal With A Focus On Theory
Formation Of Cyanamide–glyoxal Oligomers In Aqueous Environments Relevant To Primeval And Astrochemical Scenarios: A Spectroscopic And Theoretical Study
On The Asymmetric Autocatalysis Of Aldol Reactions: The Case Of 4-Nitrobenzaldehyde And Acetone. A Critical Appraisal With A Focus On Theory
Formation Of Cyanamide–glyoxal Oligomers In Aqueous Environments Relevant To Primeval And Astrochemical Scenarios: A Spectroscopic And Theoretical Study
Highly Efficient Nitrobenzene And Alkyl/aryl Azide Reduction In Stainless Steel Jars Without Catalyst Addition
Formation Of Cyanamide–glyoxal Oligomers In Aqueous Environments Relevant To Primeval And Astrochemical Scenarios: A Spectroscopic And Theoretical Study
Highly Efficient Nitrobenzene And Alkyl/aryl Azide Reduction In Stainless Steel Jars Without Catalyst Addition
On The Dual Reactivity Of A Janus-Type Mesoionic Dipole: Experiments And Theoretical Validation
Highly Efficient Nitrobenzene And Alkyl/aryl Azide Reduction In Stainless Steel Jars Without Catalyst Addition
On The Dual Reactivity Of A Janus-Type Mesoionic Dipole: Experiments And Theoretical Validation
Mechanistic Studies Of 1,3-Dipolar Cycloadditions Of Bicyclic Thioisomünchnones With Alkenes. A Computational Rationale Focused On Donor-Acceptor Interactions
On The Dual Reactivity Of A Janus-Type Mesoionic Dipole: Experiments And Theoretical Validation
Mechanistic Studies Of 1,3-Dipolar Cycloadditions Of Bicyclic Thioisomünchnones With Alkenes. A Computational Rationale Focused On Donor-Acceptor Interactions
Effects Of Ultrasonic And Hydrodynamic Cavitation On The Treatment Of Cork Wastewater By Flocculation And Fenton Processes
Mechanistic Studies Of 1,3-Dipolar Cycloadditions Of Bicyclic Thioisomünchnones With Alkenes. A Computational Rationale Focused On Donor-Acceptor Interactions
Effects Of Ultrasonic And Hydrodynamic Cavitation On The Treatment Of Cork Wastewater By Flocculation And Fenton Processes
Microwave Chemistry: History, Development And Legacy
Effects Of Ultrasonic And Hydrodynamic Cavitation On The Treatment Of Cork Wastewater By Flocculation And Fenton Processes
Microwave Chemistry: History, Development And Legacy
Merging Metallic Catalysts And Sonication: A Periodic Table Overview
Microwave Chemistry: History, Development And Legacy
Merging Metallic Catalysts And Sonication: A Periodic Table Overview
Cycloadditions With Mesoionic Dipoles: Strategy And Control
Merging Metallic Catalysts And Sonication: A Periodic Table Overview
Cycloadditions With Mesoionic Dipoles: Strategy And Control
Assessing Stereoelectronic Effects In Dipolar Cycloadditions Yielding Fused Thiazolopyridone Rings
Cycloadditions With Mesoionic Dipoles: Strategy And Control
Assessing Stereoelectronic Effects In Dipolar Cycloadditions Yielding Fused Thiazolopyridone Rings
¿qué Sabemos De La Talidomida?
Assessing Stereoelectronic Effects In Dipolar Cycloadditions Yielding Fused Thiazolopyridone Rings
¿qué Sabemos De La Talidomida?
Homochirogenesis And The Emergence Of Lifelike Structures
¿qué Sabemos De La Talidomida?
Homochirogenesis And The Emergence Of Lifelike Structures
Prebiotic-Like Condensations Of Cyanamide And Glyoxal: Revisiting Intractable Biotars
Homochirogenesis And The Emergence Of Lifelike Structures
Prebiotic-Like Condensations Of Cyanamide And Glyoxal: Revisiting Intractable Biotars
Ultrasound And Green Chemistry - Further Comments
Prebiotic-Like Condensations Of Cyanamide And Glyoxal: Revisiting Intractable Biotars
Ultrasound And Green Chemistry - Further Comments
Enantiomer-Specific Oriented Attachment Of Guanidine Carbonate Crystals
Ultrasound And Green Chemistry - Further Comments
Enantiomer-Specific Oriented Attachment Of Guanidine Carbonate Crystals
Peer Review: From Recognition To Improved Practices
Enantiomer-Specific Oriented Attachment Of Guanidine Carbonate Crystals
Peer Review: From Recognition To Improved Practices
On The Plausibility Of Pseudosugar Formation In Cometary Ices And Oxygen-Rich Tholins
Peer Review: From Recognition To Improved Practices
On The Plausibility Of Pseudosugar Formation In Cometary Ices And Oxygen-Rich Tholins
A Further Look At Π-Delocalization And Hydrogen Bonding In 2-Arylmalondialdehydes
On The Plausibility Of Pseudosugar Formation In Cometary Ices And Oxygen-Rich Tholins
A Further Look At Π-Delocalization And Hydrogen Bonding In 2-Arylmalondialdehydes
Oriented Attachment By Enantioselective Facet Recognition In Millimeter-Sized Gypsum Crystals
A Further Look At Π-Delocalization And Hydrogen Bonding In 2-Arylmalondialdehydes
Oriented Attachment By Enantioselective Facet Recognition In Millimeter-Sized Gypsum Crystals
Computational Insights Into Cycloadditions Of Thioisomünchnones With Acetylenes: How Does Sulfur Escape From Cycloadducts?
Oriented Attachment By Enantioselective Facet Recognition In Millimeter-Sized Gypsum Crystals
Computational Insights Into Cycloadditions Of Thioisomünchnones With Acetylenes: How Does Sulfur Escape From Cycloadducts?
Jjl: More Than An Educator
Computational Insights Into Cycloadditions Of Thioisomünchnones With Acetylenes: How Does Sulfur Escape From Cycloadducts?
Jjl: More Than An Educator
Interplay Between Mechanochemistry And Sonochemistry
Jjl: More Than An Educator
Interplay Between Mechanochemistry And Sonochemistry
Crystallization Of Chiral Molecules
Interplay Between Mechanochemistry And Sonochemistry
Crystallization Of Chiral Molecules
Enabling Technologies Built On A Sonochemical Platform: Challenges And Opportunities
Crystallization Of Chiral Molecules
Enabling Technologies Built On A Sonochemical Platform: Challenges And Opportunities
Complexes Of Peracetylated Cyclodextrin In A Non-Aqueous Aprotic Medium: The Role Of Residual Water
Enabling Technologies Built On A Sonochemical Platform: Challenges And Opportunities
Complexes Of Peracetylated Cyclodextrin In A Non-Aqueous Aprotic Medium: The Role Of Residual Water
Erratum: Reconfiguration Of Stereoisomers Under Sonomechanical Activation (Angewandte Chemie - International Edition (2010) (49) Doi: 10.1002/anie.201001360)
Complexes Of Peracetylated Cyclodextrin In A Non-Aqueous Aprotic Medium: The Role Of Residual Water
Erratum: Reconfiguration Of Stereoisomers Under Sonomechanical Activation (Angewandte Chemie - International Edition (2010) (49) Doi: 10.1002/anie.201001360)
Adding Only One Priority Rule Allows Extending Cip Rules To Supramolecular Systems
Erratum: Reconfiguration Of Stereoisomers Under Sonomechanical Activation (Angewandte Chemie - International Edition (2010) (49) Doi: 10.1002/anie.201001360)
Adding Only One Priority Rule Allows Extending Cip Rules To Supramolecular Systems
Rethinking Aromaticity In H-Bonded Systems. Caveats For Transition Structures Involving Hydrogen Transfer And Π-Delocalization
Adding Only One Priority Rule Allows Extending Cip Rules To Supramolecular Systems
Rethinking Aromaticity In H-Bonded Systems. Caveats For Transition Structures Involving Hydrogen Transfer And Π-Delocalization
Pseudo-Cyclic Structures Of Mono- And Di-Azaderivatives Of Malondialdehydes. Synthesis And Conformational Disentanglement By Computational Analyses
Rethinking Aromaticity In H-Bonded Systems. Caveats For Transition Structures Involving Hydrogen Transfer And Π-Delocalization
Pseudo-Cyclic Structures Of Mono- And Di-Azaderivatives Of Malondialdehydes. Synthesis And Conformational Disentanglement By Computational Analyses
Stepwise Formation Of 1,3-Diazolium-4-Thiolates By Münchnone Cycloadditions: Promising Candidates For Nonlinear Optics
Pseudo-Cyclic Structures Of Mono- And Di-Azaderivatives Of Malondialdehydes. Synthesis And Conformational Disentanglement By Computational Analyses
Stepwise Formation Of 1,3-Diazolium-4-Thiolates By Münchnone Cycloadditions: Promising Candidates For Nonlinear Optics
Hydrazones From Hydroxy Naphthaldehydes. Part 2. Condensations With Aromatic N-Aminoheterocycles And Elucidation Of Tautomeric Structures
Stepwise Formation Of 1,3-Diazolium-4-Thiolates By Münchnone Cycloadditions: Promising Candidates For Nonlinear Optics
Hydrazones From Hydroxy Naphthaldehydes. Part 2. Condensations With Aromatic N-Aminoheterocycles And Elucidation Of Tautomeric Structures
Glycerol: A Solvent And A Building Block Of Choice For Microwave And Ultrasound Irradiation Procedures
Hydrazones From Hydroxy Naphthaldehydes. Part 2. Condensations With Aromatic N-Aminoheterocycles And Elucidation Of Tautomeric Structures
Glycerol: A Solvent And A Building Block Of Choice For Microwave And Ultrasound Irradiation Procedures
Non-Covalent Derivatization Of Aminosilanized Titanium Alloy Implants Silver-Enhanced Coating Of Antibacterial Organics
Glycerol: A Solvent And A Building Block Of Choice For Microwave And Ultrasound Irradiation Procedures
Non-Covalent Derivatization Of Aminosilanized Titanium Alloy Implants Silver-Enhanced Coating Of Antibacterial Organics
Microwave-Assisted Synthesis Of N-Heterocycles In Medicinal Chemistry
Non-Covalent Derivatization Of Aminosilanized Titanium Alloy Implants Silver-Enhanced Coating Of Antibacterial Organics
Microwave-Assisted Synthesis Of N-Heterocycles In Medicinal Chemistry
Enantiomer-Specific Oriented Attachment: Formation Of Macroscopic Homochiral Crystal Aggregates From A Racemic System
Microwave-Assisted Synthesis Of N-Heterocycles In Medicinal Chemistry
Enantiomer-Specific Oriented Attachment: Formation Of Macroscopic Homochiral Crystal Aggregates From A Racemic System
On The Mechanochemical Activation By Ultrasound
Enantiomer-Specific Oriented Attachment: Formation Of Macroscopic Homochiral Crystal Aggregates From A Racemic System
On The Mechanochemical Activation By Ultrasound
Early History Of The Recognition Of Molecular Biochirality
On The Mechanochemical Activation By Ultrasound
Early History Of The Recognition Of Molecular Biochirality
The Combined Use Of Microwaves And Ultrasound: Methods And Practice
Early History Of The Recognition Of Molecular Biochirality
The Combined Use Of Microwaves And Ultrasound: Methods And Practice
Pharmaceutical And Nutraceutical Compounds From Natural Matrices
The Combined Use Of Microwaves And Ultrasound: Methods And Practice
Pharmaceutical And Nutraceutical Compounds From Natural Matrices
Controlled Silanization-Amination Reactions On The Ti6al4v Surface For Biomedical Applications
Pharmaceutical And Nutraceutical Compounds From Natural Matrices
Controlled Silanization-Amination Reactions On The Ti6al4v Surface For Biomedical Applications
Complementary And Synergic Effects Of Microwaves And Ultrasound In Metal-Assisted Synthesis
Controlled Silanization-Amination Reactions On The Ti6al4v Surface For Biomedical Applications
Complementary And Synergic Effects Of Microwaves And Ultrasound In Metal-Assisted Synthesis
On The Physical Basis Of Asymmetry And Homochirality
Complementary And Synergic Effects Of Microwaves And Ultrasound In Metal-Assisted Synthesis
On The Physical Basis Of Asymmetry And Homochirality
Metrics: Allow More Gradual Progress
On The Physical Basis Of Asymmetry And Homochirality
Metrics: Allow More Gradual Progress
Merging Microfluidics And Sonochemistry: Towards Greener And More Efficient Micro-Sono-Reactors
Metrics: Allow More Gradual Progress
Merging Microfluidics And Sonochemistry: Towards Greener And More Efficient Micro-Sono-Reactors
On The Prebiotic Synthesis Of D-Sugars Catalyzed By L-Peptides: Assessments From First-Principles Calculations
Merging Microfluidics And Sonochemistry: Towards Greener And More Efficient Micro-Sono-Reactors
On The Prebiotic Synthesis Of D-Sugars Catalyzed By L-Peptides: Assessments From First-Principles Calculations
Comment On Enantiomer Resolution By Pressure Increase: Inferences From Experimental And Topological Results For The Binary Enantiomer System (R)- And (S)-Mandelic Acid
On The Prebiotic Synthesis Of D-Sugars Catalyzed By L-Peptides: Assessments From First-Principles Calculations
Comment On Enantiomer Resolution By Pressure Increase: Inferences From Experimental And Topological Results For The Binary Enantiomer System (R)- And (S)-Mandelic Acid
Enantioenrichment In Sublimed Amino Acid Mixtures
Comment On Enantiomer Resolution By Pressure Increase: Inferences From Experimental And Topological Results For The Binary Enantiomer System (R)- And (S)-Mandelic Acid
Enantioenrichment In Sublimed Amino Acid Mixtures
Mechanochemistry: Measuring The Force Of Sound
Enantioenrichment In Sublimed Amino Acid Mixtures
Mechanochemistry: Measuring The Force Of Sound
Harnessing Mechanochemical Effects With Ultrasound-Induced Reactions
Mechanochemistry: Measuring The Force Of Sound
Harnessing Mechanochemical Effects With Ultrasound-Induced Reactions
Fast And Reliable Location Of Stationary Points In A Reaction Path
Harnessing Mechanochemical Effects With Ultrasound-Induced Reactions
Fast And Reliable Location Of Stationary Points In A Reaction Path
Reticulated Pd(Ii)/cu(I) Cyclodextrin Complexes As Recyclable Green Catalyst For Sonogashira Alkynylation
Fast And Reliable Location Of Stationary Points In A Reaction Path
Reticulated Pd(Ii)/cu(I) Cyclodextrin Complexes As Recyclable Green Catalyst For Sonogashira Alkynylation
Combined Ultrasound- Microwave Technologies
Reticulated Pd(Ii)/cu(I) Cyclodextrin Complexes As Recyclable Green Catalyst For Sonogashira Alkynylation
Combined Ultrasound- Microwave Technologies
Introduction To Sonochemistry: A Historical And Conceptual Overview
Combined Ultrasound- Microwave Technologies
Introduction To Sonochemistry: A Historical And Conceptual Overview
Homochirality Beyond Grinding: Deracemizing Chiral Crystals By Temperature Gradient Under Boiling
Introduction To Sonochemistry: A Historical And Conceptual Overview
Homochirality Beyond Grinding: Deracemizing Chiral Crystals By Temperature Gradient Under Boiling
Tautomerism In Schiff Bases. The Cases Of 2-Hydroxy-1-Naphthaldehyde And 1-Hydroxy-2-Naphthaldehyde Investigated In Solution And The Solid State
Homochirality Beyond Grinding: Deracemizing Chiral Crystals By Temperature Gradient Under Boiling
Tautomerism In Schiff Bases. The Cases Of 2-Hydroxy-1-Naphthaldehyde And 1-Hydroxy-2-Naphthaldehyde Investigated In Solution And The Solid State
Asymmetric Amplification In Amino Acid Sublimation Involving Racemic Compound To Conglomerate Conversion
Tautomerism In Schiff Bases. The Cases Of 2-Hydroxy-1-Naphthaldehyde And 1-Hydroxy-2-Naphthaldehyde Investigated In Solution And The Solid State
Asymmetric Amplification In Amino Acid Sublimation Involving Racemic Compound To Conglomerate Conversion
On The Enhanced Reactivity And Selectivity Of Triazole Formation In Molecular Flasks. A Theoretical Rationale
Asymmetric Amplification In Amino Acid Sublimation Involving Racemic Compound To Conglomerate Conversion
On The Enhanced Reactivity And Selectivity Of Triazole Formation In Molecular Flasks. A Theoretical Rationale
A Bioinspired Look At The Glucosinolate Metabolic Pathway. Structural Insights Into The Reaction Of Benzyl Isothiocyanate And D-Glucosamine
On The Enhanced Reactivity And Selectivity Of Triazole Formation In Molecular Flasks. A Theoretical Rationale
A Bioinspired Look At The Glucosinolate Metabolic Pathway. Structural Insights Into The Reaction Of Benzyl Isothiocyanate And D-Glucosamine
On The Chiral Homogeneity Of Nature: From Atoms To Small Molecules
A Bioinspired Look At The Glucosinolate Metabolic Pathway. Structural Insights Into The Reaction Of Benzyl Isothiocyanate And D-Glucosamine
On The Chiral Homogeneity Of Nature: From Atoms To Small Molecules
Assessing Molecular Chirality With Twisted Light. Comment On Photochirogenesis: Photochemical Models On The Absolute Asymmetric Formation Of Amino Acids In Interstellar Space By Uwe J. Meierhenrich Et Al.
On The Chiral Homogeneity Of Nature: From Atoms To Small Molecules
Assessing Molecular Chirality With Twisted Light. Comment On Photochirogenesis: Photochemical Models On The Absolute Asymmetric Formation Of Amino Acids In Interstellar Space By Uwe J. Meierhenrich Et Al.
Schiff Bases From Tris And Ortho-Hydroxyarenecarbaldehydes: Structures And Tautomeric Equilibria In The Solid State And In Solution
Assessing Molecular Chirality With Twisted Light. Comment On Photochirogenesis: Photochemical Models On The Absolute Asymmetric Formation Of Amino Acids In Interstellar Space By Uwe J. Meierhenrich Et Al.
Schiff Bases From Tris And Ortho-Hydroxyarenecarbaldehydes: Structures And Tautomeric Equilibria In The Solid State And In Solution
A Quantitative Structure-Reactivity Relationship In N-Acetyl Oxazolidines: An Electrostatic Interaction Controls Rotamer Population
Schiff Bases From Tris And Ortho-Hydroxyarenecarbaldehydes: Structures And Tautomeric Equilibria In The Solid State And In Solution
A Quantitative Structure-Reactivity Relationship In N-Acetyl Oxazolidines: An Electrostatic Interaction Controls Rotamer Population
Assessing The Whole Range Of Cuaac Mechanisms By Dft Calculations - On The Intermediacy Of Copper Acetylides
A Quantitative Structure-Reactivity Relationship In N-Acetyl Oxazolidines: An Electrostatic Interaction Controls Rotamer Population
Assessing The Whole Range Of Cuaac Mechanisms By Dft Calculations - On The Intermediacy Of Copper Acetylides
Hydrazones From Hydroxy Naphthaldehydes And N-Aminoheterocycles: Structure And Stereodynamics
Assessing The Whole Range Of Cuaac Mechanisms By Dft Calculations - On The Intermediacy Of Copper Acetylides
Hydrazones From Hydroxy Naphthaldehydes And N-Aminoheterocycles: Structure And Stereodynamics
Assessing Performance Through Understanding
Hydrazones From Hydroxy Naphthaldehydes And N-Aminoheterocycles: Structure And Stereodynamics
Assessing Performance Through Understanding
Power Ultrasound In Metal-Assisted Synthesis: From Classical Barbier-Like Reactions To Click Chemistry
Assessing Performance Through Understanding
Power Ultrasound In Metal-Assisted Synthesis: From Classical Barbier-Like Reactions To Click Chemistry
Push-Pull 1,3-Thiazolium-5-Thiolates. Formation Via Concerted And Stepwise Pathways, And Theoretical Evaluation Of Nlo Properties
Power Ultrasound In Metal-Assisted Synthesis: From Classical Barbier-Like Reactions To Click Chemistry
Push-Pull 1,3-Thiazolium-5-Thiolates. Formation Via Concerted And Stepwise Pathways, And Theoretical Evaluation Of Nlo Properties
Schiff Bases From Tris And Formylpyridines: Structure And Mechanistic Rationale Aided By Dft Calculations
Push-Pull 1,3-Thiazolium-5-Thiolates. Formation Via Concerted And Stepwise Pathways, And Theoretical Evaluation Of Nlo Properties
Schiff Bases From Tris And Formylpyridines: Structure And Mechanistic Rationale Aided By Dft Calculations
An Anomeric Effect Drives The Regiospecific Ring-Opening Of 1,3-Oxazolidines Under Acetylating Conditions
Schiff Bases From Tris And Formylpyridines: Structure And Mechanistic Rationale Aided By Dft Calculations
An Anomeric Effect Drives The Regiospecific Ring-Opening Of 1,3-Oxazolidines Under Acetylating Conditions
Reconfiguration Of Stereoisomers Under Sonomechanical Activation
An Anomeric Effect Drives The Regiospecific Ring-Opening Of 1,3-Oxazolidines Under Acetylating Conditions
Reconfiguration Of Stereoisomers Under Sonomechanical Activation
Metrics: Include Refereeing As Part Of Performance Rating
Reconfiguration Of Stereoisomers Under Sonomechanical Activation
Metrics: Include Refereeing As Part Of Performance Rating
Unusual Aryl Migration In A Mesomeric Betaine In The Solid And Liquid State: Mechanistic Insights Into The Snar Reaction
Metrics: Include Refereeing As Part Of Performance Rating
Unusual Aryl Migration In A Mesomeric Betaine In The Solid And Liquid State: Mechanistic Insights Into The Snar Reaction
Homochirality And Chemical Evolution: New Vistas And Reflections On Recent Models
Unusual Aryl Migration In A Mesomeric Betaine In The Solid And Liquid State: Mechanistic Insights Into The Snar Reaction
Homochirality And Chemical Evolution: New Vistas And Reflections On Recent Models
Sonication-Assisted Fabrication And Post-Synthetic Modifications Of Graphene-Like Materials
Homochirality And Chemical Evolution: New Vistas And Reflections On Recent Models
Sonication-Assisted Fabrication And Post-Synthetic Modifications Of Graphene-Like Materials
Alkyne-Azide Click Reaction Catalyzed By Metallic Copper Under Ultrasound
Sonication-Assisted Fabrication And Post-Synthetic Modifications Of Graphene-Like Materials
Alkyne-Azide Click Reaction Catalyzed By Metallic Copper Under Ultrasound
A New Model For Mapping The Peptide Backbone: Predicting Proton Chemical Shifts In Proteins
Alkyne-Azide Click Reaction Catalyzed By Metallic Copper Under Ultrasound
A New Model For Mapping The Peptide Backbone: Predicting Proton Chemical Shifts In Proteins
Schiff Bases From D-Glucosamine And Aliphatic Ketones
A New Model For Mapping The Peptide Backbone: Predicting Proton Chemical Shifts In Proteins
Schiff Bases From D-Glucosamine And Aliphatic Ketones
A New Pilot Flow Reactor For High-Intensity Ultrasound Irradiation. Application To The Synthesis Of Biodiesel
Schiff Bases From D-Glucosamine And Aliphatic Ketones
A New Pilot Flow Reactor For High-Intensity Ultrasound Irradiation. Application To The Synthesis Of Biodiesel
Evolving Alchemy Into Chemistry: No Longer A Dichotomy
A New Pilot Flow Reactor For High-Intensity Ultrasound Irradiation. Application To The Synthesis Of Biodiesel
Evolving Alchemy Into Chemistry: No Longer A Dichotomy
Dissecting Competitive Mechanisms: Thionation Vs. Cycloaddition In The Reaction Of Thioisomünchnones With Isothiocyanates Under Microwave Irradiation
Evolving Alchemy Into Chemistry: No Longer A Dichotomy
Dissecting Competitive Mechanisms: Thionation Vs. Cycloaddition In The Reaction Of Thioisomünchnones With Isothiocyanates Under Microwave Irradiation
Molecular Self-Assembly And Patterning Induced By Sound Waves. The Case Of Gelation
Dissecting Competitive Mechanisms: Thionation Vs. Cycloaddition In The Reaction Of Thioisomünchnones With Isothiocyanates Under Microwave Irradiation
Molecular Self-Assembly And Patterning Induced By Sound Waves. The Case Of Gelation
Thionation Of Mesoionics With Isothiocyanates: Evidence Supporting A Four-Step Domino Process And Ruling Out A [2 + 2] Mechanism
Molecular Self-Assembly And Patterning Induced By Sound Waves. The Case Of Gelation
Thionation Of Mesoionics With Isothiocyanates: Evidence Supporting A Four-Step Domino Process And Ruling Out A [2 + 2] Mechanism
Transition Metals In Radiation-Induced Reactions For Organic Synthesis: Applications Of Ultrasound
Thionation Of Mesoionics With Isothiocyanates: Evidence Supporting A Four-Step Domino Process And Ruling Out A [2 + 2] Mechanism
Transition Metals In Radiation-Induced Reactions For Organic Synthesis: Applications Of Ultrasound
Pd-Catalyzed Reactions Promoted By Ultrasound And/or Microwave Irradiation
Transition Metals In Radiation-Induced Reactions For Organic Synthesis: Applications Of Ultrasound
Pd-Catalyzed Reactions Promoted By Ultrasound And/or Microwave Irradiation
On Cavitation And Chirality: A Further Assessment
Pd-Catalyzed Reactions Promoted By Ultrasound And/or Microwave Irradiation
On Cavitation And Chirality: A Further Assessment
An Efficient And Highly Diastereoselective Synthesis Of C-Glycosylated 1,3-Oxazolidines From N-Methyl-D-Glucamine
On Cavitation And Chirality: A Further Assessment
An Efficient And Highly Diastereoselective Synthesis Of C-Glycosylated 1,3-Oxazolidines From N-Methyl-D-Glucamine
A Family Of Hydrogels Based On Ureido-Linked Aminopolyol-Derived Amphiphiles And Bolaamphiphiles: Synthesis, Gelation Under Thermal And Sonochemical Stimuli, And Mesomorphic Characterization
An Efficient And Highly Diastereoselective Synthesis Of C-Glycosylated 1,3-Oxazolidines From N-Methyl-D-Glucamine
A Family Of Hydrogels Based On Ureido-Linked Aminopolyol-Derived Amphiphiles And Bolaamphiphiles: Synthesis, Gelation Under Thermal And Sonochemical Stimuli, And Mesomorphic Characterization
Sublime Arguments: Rethinking The Generation Of Homochirality Under Prebiotic Conditions
A Family Of Hydrogels Based On Ureido-Linked Aminopolyol-Derived Amphiphiles And Bolaamphiphiles: Synthesis, Gelation Under Thermal And Sonochemical Stimuli, And Mesomorphic Characterization
Sublime Arguments: Rethinking The Generation Of Homochirality Under Prebiotic Conditions
Stepwise Cycloadditions Of Mesoionic Systems: Thionation Of Thioisomunchnones By Isothiocyanates
Sublime Arguments: Rethinking The Generation Of Homochirality Under Prebiotic Conditions
Stepwise Cycloadditions Of Mesoionic Systems: Thionation Of Thioisomunchnones By Isothiocyanates
Chiral N-Acyloxazolidines: Synthesis, Structure, And Mechanistic Insights
Stepwise Cycloadditions Of Mesoionic Systems: Thionation Of Thioisomunchnones By Isothiocyanates
Chiral N-Acyloxazolidines: Synthesis, Structure, And Mechanistic Insights
Improved Extraction Of Vegetable Oils Under High-Intensity Ultrasound And/or Microwaves
Chiral N-Acyloxazolidines: Synthesis, Structure, And Mechanistic Insights
Improved Extraction Of Vegetable Oils Under High-Intensity Ultrasound And/or Microwaves
Chirality And Chemical Processes: A Few Afterthoughts
Improved Extraction Of Vegetable Oils Under High-Intensity Ultrasound And/or Microwaves
Chirality And Chemical Processes: A Few Afterthoughts
Ultrasound-Induced Activation Of Metals: Principles And Applications In Organic Synthesis
Chirality And Chemical Processes: A Few Afterthoughts
Ultrasound-Induced Activation Of Metals: Principles And Applications In Organic Synthesis
Sonochemistry
Ultrasound-Induced Activation Of Metals: Principles And Applications In Organic Synthesis
Sonochemistry
Chemical Reaction To The Many-Worlds Hypothesis [3]
Sonochemistry
Chemical Reaction To The Many-Worlds Hypothesis [3]
Improved Protocols For Microwave-Assisted Cu(I)-Catalyzed Huisgen 1,3-Dipolar Cycloadditions
Chemical Reaction To The Many-Worlds Hypothesis [3]
Improved Protocols For Microwave-Assisted Cu(I)-Catalyzed Huisgen 1,3-Dipolar Cycloadditions
Forcing And Controlling Chemical Reactions With Ultrasound
Improved Protocols For Microwave-Assisted Cu(I)-Catalyzed Huisgen 1,3-Dipolar Cycloadditions
Forcing And Controlling Chemical Reactions With Ultrasound
Tracing The Origins And Evolution Of Chirality And Handedness In Chemical Language
Forcing And Controlling Chemical Reactions With Ultrasound
Tracing The Origins And Evolution Of Chirality And Handedness In Chemical Language
The Combined Use Of Microwaves And Ultrasound: Improved Tools In Process Chemistry And Organic Synthesis
Tracing The Origins And Evolution Of Chirality And Handedness In Chemical Language
The Combined Use Of Microwaves And Ultrasound: Improved Tools In Process Chemistry And Organic Synthesis
Extraction Of Flavourings From Natural Sources
The Combined Use Of Microwaves And Ultrasound: Improved Tools In Process Chemistry And Organic Synthesis
Extraction Of Flavourings From Natural Sources
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
Extraction Of Flavourings From Natural Sources
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
Construction Of C-Nucleosides Diversified By [3+2] Cycloaddition From A Sugar-Based Mesoionic Ring
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
Construction Of C-Nucleosides Diversified By [3+2] Cycloaddition From A Sugar-Based Mesoionic Ring
Greener Media In Chemical Synthesis And Processing
Construction Of C-Nucleosides Diversified By [3+2] Cycloaddition From A Sugar-Based Mesoionic Ring
Greener Media In Chemical Synthesis And Processing
A One-Pot Domino Reaction In Constructing Isoorotate Bases And Their Nucleosides
Greener Media In Chemical Synthesis And Processing
A One-Pot Domino Reaction In Constructing Isoorotate Bases And Their Nucleosides
Synthesis Of Sugar Isocyanates And Their Application To The Formation Of Ureido-Linked Disaccharides
A One-Pot Domino Reaction In Constructing Isoorotate Bases And Their Nucleosides
Synthesis Of Sugar Isocyanates And Their Application To The Formation Of Ureido-Linked Disaccharides
Power Ultrasound In Organic Synthesis: Moving Cavitational Chemistry From Academia To Innovative And Large-Scale Applications
Synthesis Of Sugar Isocyanates And Their Application To The Formation Of Ureido-Linked Disaccharides
Power Ultrasound In Organic Synthesis: Moving Cavitational Chemistry From Academia To Innovative And Large-Scale Applications
Sonochemical Cycloadditions In Ionic Liquids. Lessons From Model Cases Involving Common Dienes And Carbonyl Dienophiles
Power Ultrasound In Organic Synthesis: Moving Cavitational Chemistry From Academia To Innovative And Large-Scale Applications
Sonochemical Cycloadditions In Ionic Liquids. Lessons From Model Cases Involving Common Dienes And Carbonyl Dienophiles
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 4: Absolute Stereochemistry Of Carbohydrate-Based Imidazolidine-2-Ones And 2-Thiones With Axial And Central Chirality
Sonochemical Cycloadditions In Ionic Liquids. Lessons From Model Cases Involving Common Dienes And Carbonyl Dienophiles
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 4: Absolute Stereochemistry Of Carbohydrate-Based Imidazolidine-2-Ones And 2-Thiones With Axial And Central Chirality
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 3: Rotational Isomerism Of Sterically Hindered Heteroaryl Imidazolidine-2-Ones And 2-Thiones
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 4: Absolute Stereochemistry Of Carbohydrate-Based Imidazolidine-2-Ones And 2-Thiones With Axial And Central Chirality
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 3: Rotational Isomerism Of Sterically Hindered Heteroaryl Imidazolidine-2-Ones And 2-Thiones
Exploiting Synthetic Chemistry With Mesoionic Rings: Improvements Achieved With Thioisomünchnones
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 3: Rotational Isomerism Of Sterically Hindered Heteroaryl Imidazolidine-2-Ones And 2-Thiones
Exploiting Synthetic Chemistry With Mesoionic Rings: Improvements Achieved With Thioisomünchnones
Ultrasonics Sonochemistry: Preface
Exploiting Synthetic Chemistry With Mesoionic Rings: Improvements Achieved With Thioisomünchnones
Ultrasonics Sonochemistry: Preface
Starting From Scratch: The Rise And Fate Of Carbon Atoms
Ultrasonics Sonochemistry: Preface
Starting From Scratch: The Rise And Fate Of Carbon Atoms
Chemistry And Luminescence
Starting From Scratch: The Rise And Fate Of Carbon Atoms
Chemistry And Luminescence
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
Chemistry And Luminescence
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
The Road To Chemical Names And Eponyms: Discovery, Priority, And Credit
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
The Road To Chemical Names And Eponyms: Discovery, Priority, And Credit
Symmetry Breaking: An Epistemological Note
The Road To Chemical Names And Eponyms: Discovery, Priority, And Credit
Symmetry Breaking: An Epistemological Note
Symmetry Breaking By Spontaneous Crystallization - Is It The Most Plausible Source Of Terrestrial Handedness We Have Long Been Looking For? - A Reappraisal
Symmetry Breaking: An Epistemological Note
Symmetry Breaking By Spontaneous Crystallization - Is It The Most Plausible Source Of Terrestrial Handedness We Have Long Been Looking For? - A Reappraisal
Evolutionary Biology And Chemical Geology: A Timely Marriage
Symmetry Breaking By Spontaneous Crystallization - Is It The Most Plausible Source Of Terrestrial Handedness We Have Long Been Looking For? - A Reappraisal
Evolutionary Biology And Chemical Geology: A Timely Marriage
Confidential Reports May Improve Peer Review [3]
Evolutionary Biology And Chemical Geology: A Timely Marriage
Confidential Reports May Improve Peer Review [3]
Erratum: Thermal And Sonochemical Studies On The Diels-Alder Cycloadditions Of Masked O-Benzoquinones With Furans: New Insights Into The Reaction Mechanism (Journal Of Organic Chemistry (2003) 68 (7193-7203))
Confidential Reports May Improve Peer Review [3]
Erratum: Thermal And Sonochemical Studies On The Diels-Alder Cycloadditions Of Masked O-Benzoquinones With Furans: New Insights Into The Reaction Mechanism (Journal Of Organic Chemistry (2003) 68 (7193-7203))
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Erratum: Thermal And Sonochemical Studies On The Diels-Alder Cycloadditions Of Masked O-Benzoquinones With Furans: New Insights Into The Reaction Mechanism (Journal Of Organic Chemistry (2003) 68 (7193-7203))
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Thermal And Sonochemical Studies On The Diels-Alder Cycloadditions Of Masked O-Benzoquinones With Furans: New Insights Into The Reaction Mechanism
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Thermal And Sonochemical Studies On The Diels-Alder Cycloadditions Of Masked O-Benzoquinones With Furans: New Insights Into The Reaction Mechanism
1,3-Dipolar Cycloaddition Of 2-Dialkylaminothioisomünchnones With Aliphatic Aldehydes: Synthesis Of Β-Lactams And Thiiranes, Structure Elucidation, And Rationale For Chemoselective Fragmentation Of Cycloadducts
Thermal And Sonochemical Studies On The Diels-Alder Cycloadditions Of Masked O-Benzoquinones With Furans: New Insights Into The Reaction Mechanism
1,3-Dipolar Cycloaddition Of 2-Dialkylaminothioisomünchnones With Aliphatic Aldehydes: Synthesis Of Β-Lactams And Thiiranes, Structure Elucidation, And Rationale For Chemoselective Fragmentation Of Cycloadducts
Conformation Of Secondary Amides. A Predictive Algorithm That Correlates Dft-Calculated Structures And Experimental Proton Chemical Shifts
1,3-Dipolar Cycloaddition Of 2-Dialkylaminothioisomünchnones With Aliphatic Aldehydes: Synthesis Of Β-Lactams And Thiiranes, Structure Elucidation, And Rationale For Chemoselective Fragmentation Of Cycloadducts
Conformation Of Secondary Amides. A Predictive Algorithm That Correlates Dft-Calculated Structures And Experimental Proton Chemical Shifts
Sonochemical Effects In The Additions Of Furan To Masked Ortho-Benzoquinones
Conformation Of Secondary Amides. A Predictive Algorithm That Correlates Dft-Calculated Structures And Experimental Proton Chemical Shifts
Sonochemical Effects In The Additions Of Furan To Masked Ortho-Benzoquinones
What Does Elementary Chirality Have To Do With Neutrinos?
Sonochemical Effects In The Additions Of Furan To Masked Ortho-Benzoquinones
What Does Elementary Chirality Have To Do With Neutrinos?
How Serendipity Led To An Early Treatment [2]
What Does Elementary Chirality Have To Do With Neutrinos?
How Serendipity Led To An Early Treatment [2]
Erratum: (Angewandte Chemie - International Edition (2002) 7 (1139-1145))
How Serendipity Led To An Early Treatment [2]
Erratum: (Angewandte Chemie - International Edition (2002) 7 (1139-1145))
Experimental And Theoretical Insights Regarding The Cycloaddition Reaction Of Carbohydrate-Based 1,2-Diaza-1,3-Butadienes And Acrylonitrile. A Model Case For The Behavior Of Chiral Azoalkenes And Unsymmetric Olefins
Erratum: (Angewandte Chemie - International Edition (2002) 7 (1139-1145))
Experimental And Theoretical Insights Regarding The Cycloaddition Reaction Of Carbohydrate-Based 1,2-Diaza-1,3-Butadienes And Acrylonitrile. A Model Case For The Behavior Of Chiral Azoalkenes And Unsymmetric Olefins
Novel Acid-Catalyzed Rearrangement Of Tetrahydro-1,2,3,4-Tetrazines: Unexpected Formation Of Glycosazones
Experimental And Theoretical Insights Regarding The Cycloaddition Reaction Of Carbohydrate-Based 1,2-Diaza-1,3-Butadienes And Acrylonitrile. A Model Case For The Behavior Of Chiral Azoalkenes And Unsymmetric Olefins
Novel Acid-Catalyzed Rearrangement Of Tetrahydro-1,2,3,4-Tetrazines: Unexpected Formation Of Glycosazones
Chirality Of Living Systems: A Helping Hand From Crystals And Oligopeptides
Novel Acid-Catalyzed Rearrangement Of Tetrahydro-1,2,3,4-Tetrazines: Unexpected Formation Of Glycosazones
Chirality Of Living Systems: A Helping Hand From Crystals And Oligopeptides
Generation And Fate Of A Novel Homochiral Mesoionic Dipole: Synthesis Of C-Nucleoside Analogs
Chirality Of Living Systems: A Helping Hand From Crystals And Oligopeptides
Generation And Fate Of A Novel Homochiral Mesoionic Dipole: Synthesis Of C-Nucleoside Analogs
Can We Predict The Conformational Preference Of Amides?
Generation And Fate Of A Novel Homochiral Mesoionic Dipole: Synthesis Of C-Nucleoside Analogs
Can We Predict The Conformational Preference Of Amides?
Carbohydrates As Chiral Controllers: Synthesis Of Dihydrothieno[2,3-C]furanones
Can We Predict The Conformational Preference Of Amides?
Carbohydrates As Chiral Controllers: Synthesis Of Dihydrothieno[2,3-C]furanones
A Cycloaddition Strategy For The Synthesis Of Thiirane-Containing Glycomimetics
Carbohydrates As Chiral Controllers: Synthesis Of Dihydrothieno[2,3-C]furanones
A Cycloaddition Strategy For The Synthesis Of Thiirane-Containing Glycomimetics
Synergic Effect Of Vicinal Stereocenters In [3 + 2] Cycloadditions Of Carbohydrate Azadipolarophiles And Mesoionic Dipoles: Origin Of Diastereofacial Selectivity
A Cycloaddition Strategy For The Synthesis Of Thiirane-Containing Glycomimetics
Synergic Effect Of Vicinal Stereocenters In [3 + 2] Cycloadditions Of Carbohydrate Azadipolarophiles And Mesoionic Dipoles: Origin Of Diastereofacial Selectivity
Three- And Four-Membered Rings From Cycloadditions Of 1,3-Thiazolium-4-Olates And Aldehydes
Synergic Effect Of Vicinal Stereocenters In [3 + 2] Cycloadditions Of Carbohydrate Azadipolarophiles And Mesoionic Dipoles: Origin Of Diastereofacial Selectivity
Three- And Four-Membered Rings From Cycloadditions Of 1,3-Thiazolium-4-Olates And Aldehydes
Elementary Asymmetry And Biochirality: No Longer Twinned
Three- And Four-Membered Rings From Cycloadditions Of 1,3-Thiazolium-4-Olates And Aldehydes
Elementary Asymmetry And Biochirality: No Longer Twinned
Conjugate Additions Of Heteronucleophiles To Enones And Alkynoates. A 'benign By Design' Functionalization Of Heteroaromatics
Elementary Asymmetry And Biochirality: No Longer Twinned
Conjugate Additions Of Heteronucleophiles To Enones And Alkynoates. A 'benign By Design' Functionalization Of Heteroaromatics
Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone-Alkene Cycloaddition Reaction
Conjugate Additions Of Heteronucleophiles To Enones And Alkynoates. A 'benign By Design' Functionalization Of Heteroaromatics
Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone-Alkene Cycloaddition Reaction
Erratum: Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone - Alkene Cycloaddition Reaction (European Journal Of Organic Chemistry (2001) (2135-2144))
Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone-Alkene Cycloaddition Reaction
Erratum: Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone - Alkene Cycloaddition Reaction (European Journal Of Organic Chemistry (2001) (2135-2144))
Reactions Of 2-Amino-2-Thiazolines With Isocyanates And Isothiocyanates. Chemical And Computational Studies On The Regioselectivity, Adduct Rearrangement, And Mechanistic Pathways
Erratum: Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone - Alkene Cycloaddition Reaction (European Journal Of Organic Chemistry (2001) (2135-2144))
Reactions Of 2-Amino-2-Thiazolines With Isocyanates And Isothiocyanates. Chemical And Computational Studies On The Regioselectivity, Adduct Rearrangement, And Mechanistic Pathways
The First Density Functional Study On The [4 + 2]-Cycloaddition Reactions Of 1,2-Diaza-1,3-Butadiene With Alkenes
Reactions Of 2-Amino-2-Thiazolines With Isocyanates And Isothiocyanates. Chemical And Computational Studies On The Regioselectivity, Adduct Rearrangement, And Mechanistic Pathways
The First Density Functional Study On The [4 + 2]-Cycloaddition Reactions Of 1,2-Diaza-1,3-Butadiene With Alkenes
Computational Studies On The Bf3-Catalyzed Cycloaddition Of Furan With Methyl Vinyl Ketone: A New Look At Lewis Acid Catalysis
The First Density Functional Study On The [4 + 2]-Cycloaddition Reactions Of 1,2-Diaza-1,3-Butadiene With Alkenes
Computational Studies On The Bf3-Catalyzed Cycloaddition Of Furan With Methyl Vinyl Ketone: A New Look At Lewis Acid Catalysis
Diastereoselective Cycloadditions Of 1,3-Thiazolium-4-Olates With Chiral 1,2-Diaza-1,3-Butadienes
Computational Studies On The Bf3-Catalyzed Cycloaddition Of Furan With Methyl Vinyl Ketone: A New Look At Lewis Acid Catalysis
Diastereoselective Cycloadditions Of 1,3-Thiazolium-4-Olates With Chiral 1,2-Diaza-1,3-Butadienes
From Parity To Chirality: Chemical Implications Revisited
Diastereoselective Cycloadditions Of 1,3-Thiazolium-4-Olates With Chiral 1,2-Diaza-1,3-Butadienes
From Parity To Chirality: Chemical Implications Revisited
Chiral Autocatalysis: Where Stereochemistry Meets The Origin Of Life
From Parity To Chirality: Chemical Implications Revisited
Chiral Autocatalysis: Where Stereochemistry Meets The Origin Of Life
Sonochemical Cycloadditions Of O-Quinones. The Search For A Cation Radical Pathway
Chiral Autocatalysis: Where Stereochemistry Meets The Origin Of Life
Sonochemical Cycloadditions Of O-Quinones. The Search For A Cation Radical Pathway
Optically Active Sugar Thioamides From Δ-Gluconolactone
Sonochemical Cycloadditions Of O-Quinones. The Search For A Cation Radical Pathway
Optically Active Sugar Thioamides From Δ-Gluconolactone
[3+2]-Cycloadditions Of 2-Aminothioisomunchnones To Alkynes: Synthetic Scope And Mechanistic Insights
Optically Active Sugar Thioamides From Δ-Gluconolactone
[3+2]-Cycloadditions Of 2-Aminothioisomunchnones To Alkynes: Synthetic Scope And Mechanistic Insights
Understanding Diastereofacial Selection In Carbohydrate-Based Domino Cycloadditions: Semiempirical And Dft Calculations
[3+2]-Cycloadditions Of 2-Aminothioisomunchnones To Alkynes: Synthetic Scope And Mechanistic Insights
Understanding Diastereofacial Selection In Carbohydrate-Based Domino Cycloadditions: Semiempirical And Dft Calculations
Expeditious Formation Of 1,2,4-Triazine Derivatives Via A Thioisomunchnone Cycloaddition Reaction
Understanding Diastereofacial Selection In Carbohydrate-Based Domino Cycloadditions: Semiempirical And Dft Calculations
Expeditious Formation Of 1,2,4-Triazine Derivatives Via A Thioisomunchnone Cycloaddition Reaction
Atropisomeric Carbohydrate Imidazolidines: A Novel Class Of Nonbiaryl Atropisomers
Expeditious Formation Of 1,2,4-Triazine Derivatives Via A Thioisomunchnone Cycloaddition Reaction
Atropisomeric Carbohydrate Imidazolidines: A Novel Class Of Nonbiaryl Atropisomers
Unexpected Formation Of Β-Lactams And Penem Isosteres From Mesoionics: Sequential Ring-Opening-Rearrangement Of [3 + 2] Cycloadducts
Atropisomeric Carbohydrate Imidazolidines: A Novel Class Of Nonbiaryl Atropisomers
Unexpected Formation Of Β-Lactams And Penem Isosteres From Mesoionics: Sequential Ring-Opening-Rearrangement Of [3 + 2] Cycloadducts
Hetero-Diels-Alder Reactions Of Homochiral 1,2-Diaza-1,3-Butadienes With Diethyl Azodicarboxylate Under Microwave Irradiation. Theoretical Rationale Of The Stereochemical Outcome
Unexpected Formation Of Β-Lactams And Penem Isosteres From Mesoionics: Sequential Ring-Opening-Rearrangement Of [3 + 2] Cycloadducts
Hetero-Diels-Alder Reactions Of Homochiral 1,2-Diaza-1,3-Butadienes With Diethyl Azodicarboxylate Under Microwave Irradiation. Theoretical Rationale Of The Stereochemical Outcome
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 1. Stereoselective Synthesis Of 1-Aryl-5-Hydroxyimidazolidine-2-Thiones And Their Transformation Into Imidazoline-2-Thiones
Hetero-Diels-Alder Reactions Of Homochiral 1,2-Diaza-1,3-Butadienes With Diethyl Azodicarboxylate Under Microwave Irradiation. Theoretical Rationale Of The Stereochemical Outcome
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 1. Stereoselective Synthesis Of 1-Aryl-5-Hydroxyimidazolidine-2-Thiones And Their Transformation Into Imidazoline-2-Thiones
Diastereoselective Cycloadditions Of Nitroalkenes As An Approach To The Assembly Of Bicyclic Nitrogen Heterocycles
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 1. Stereoselective Synthesis Of 1-Aryl-5-Hydroxyimidazolidine-2-Thiones And Their Transformation Into Imidazoline-2-Thiones
Diastereoselective Cycloadditions Of Nitroalkenes As An Approach To The Assembly Of Bicyclic Nitrogen Heterocycles
Synthetic Variations Based On Low-Valent Chromium: New Developments
Diastereoselective Cycloadditions Of Nitroalkenes As An Approach To The Assembly Of Bicyclic Nitrogen Heterocycles
Synthetic Variations Based On Low-Valent Chromium: New Developments
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 2. Atropisomeric Behavior Of Monocyclic And Bicyclic Imidazolidine-2-Ones And 2- Thiones
Synthetic Variations Based On Low-Valent Chromium: New Developments
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 2. Atropisomeric Behavior Of Monocyclic And Bicyclic Imidazolidine-2-Ones And 2- Thiones
Green Chemistry: The Sonochemical Approach
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 2. Atropisomeric Behavior Of Monocyclic And Bicyclic Imidazolidine-2-Ones And 2- Thiones
Green Chemistry: The Sonochemical Approach
Clay-Catalyzed Solventless Addition Reactions Of Furan With Α,β- Unsaturated Carbonyl Compounds
Green Chemistry: The Sonochemical Approach
Clay-Catalyzed Solventless Addition Reactions Of Furan With Α,β- Unsaturated Carbonyl Compounds
Cycloadditions With Clays And Alumina Without Solvents
Clay-Catalyzed Solventless Addition Reactions Of Furan With Α,β- Unsaturated Carbonyl Compounds
Cycloadditions With Clays And Alumina Without Solvents
The Structure Of Glycosyl Amides: A Combined Study By Nmr Spectroscopy, X-Ray Crystallography, And Computational Chemistry
Cycloadditions With Clays And Alumina Without Solvents
The Structure Of Glycosyl Amides: A Combined Study By Nmr Spectroscopy, X-Ray Crystallography, And Computational Chemistry
Absolute Asymmetric Synthesis Under Physical Fields: Facts And Fictions
The Structure Of Glycosyl Amides: A Combined Study By Nmr Spectroscopy, X-Ray Crystallography, And Computational Chemistry
Absolute Asymmetric Synthesis Under Physical Fields: Facts And Fictions
Reactions Of Thioamides With Metal Carboxylates In Organic Media
Absolute Asymmetric Synthesis Under Physical Fields: Facts And Fictions
Reactions Of Thioamides With Metal Carboxylates In Organic Media
Nonlinear Stereochemical Effects In Asymmetric Reactions
Reactions Of Thioamides With Metal Carboxylates In Organic Media
Nonlinear Stereochemical Effects In Asymmetric Reactions
Nmr Studies And Semiempirical Calculations On The Structure Of Glycoamidines
Nonlinear Stereochemical Effects In Asymmetric Reactions
Nmr Studies And Semiempirical Calculations On The Structure Of Glycoamidines
Cycloaddition Chemistry Of 1,3-Thiazolium-4-Olate Systems. Reaction With Nitroalkenes And Interpretation Of Results Using Pm3 Calculations
Nmr Studies And Semiempirical Calculations On The Structure Of Glycoamidines
Cycloaddition Chemistry Of 1,3-Thiazolium-4-Olate Systems. Reaction With Nitroalkenes And Interpretation Of Results Using Pm3 Calculations
Substrate-Controlled Stereodifferentiation Of Tandem [4 + 2]/[3 + 2] Cycloadditions By A Vicinal Carbohydrate-Based Template
Cycloaddition Chemistry Of 1,3-Thiazolium-4-Olate Systems. Reaction With Nitroalkenes And Interpretation Of Results Using Pm3 Calculations
Substrate-Controlled Stereodifferentiation Of Tandem [4 + 2]/[3 + 2] Cycloadditions By A Vicinal Carbohydrate-Based Template
A Simple, Cip-Based Notation System For The Unambiguous Specification Of Asymmetric Reactions
Substrate-Controlled Stereodifferentiation Of Tandem [4 + 2]/[3 + 2] Cycloadditions By A Vicinal Carbohydrate-Based Template
A Simple, Cip-Based Notation System For The Unambiguous Specification Of Asymmetric Reactions
Anodic Oxidation Of Thioureido Derivatives Of Biogenic Amines At A Glassy Carbon Electrode In An Aqueous Medium
A Simple, Cip-Based Notation System For The Unambiguous Specification Of Asymmetric Reactions
Anodic Oxidation Of Thioureido Derivatives Of Biogenic Amines At A Glassy Carbon Electrode In An Aqueous Medium
Münchnone-Alkene Cycloadditions: Deviations From The Fmo Theory. Theoretical Studies In The Search Of The Transition State
Anodic Oxidation Of Thioureido Derivatives Of Biogenic Amines At A Glassy Carbon Electrode In An Aqueous Medium
Münchnone-Alkene Cycloadditions: Deviations From The Fmo Theory. Theoretical Studies In The Search Of The Transition State
Synthesis Of Glycoamidines Using A Mercury-Promoted Reaction
Münchnone-Alkene Cycloadditions: Deviations From The Fmo Theory. Theoretical Studies In The Search Of The Transition State
Synthesis Of Glycoamidines Using A Mercury-Promoted Reaction
A Facile And Expeditious Entry To Acyclic Carbohydrate-Derived 1,2-Diazabutadienes
Synthesis Of Glycoamidines Using A Mercury-Promoted Reaction
A Facile And Expeditious Entry To Acyclic Carbohydrate-Derived 1,2-Diazabutadienes
A Novel Highly Diastereoselective Synthesis Of Chiral Dihydrothiophenes From Mesoionic Compounds
A Facile And Expeditious Entry To Acyclic Carbohydrate-Derived 1,2-Diazabutadienes
A Novel Highly Diastereoselective Synthesis Of Chiral Dihydrothiophenes From Mesoionic Compounds
Synthetic Organoindium Chemistry: What Makes Indium So Appealing?
A Novel Highly Diastereoselective Synthesis Of Chiral Dihydrothiophenes From Mesoionic Compounds
Synthetic Organoindium Chemistry: What Makes Indium So Appealing?
Organometallic Catalysis [2]
Synthetic Organoindium Chemistry: What Makes Indium So Appealing?
Organometallic Catalysis [2]
Cucurbituril: Supramolecular Perspectives For An Old Ligand
Organometallic Catalysis [2]
Cucurbituril: Supramolecular Perspectives For An Old Ligand
Condensation Of 2-Amino-2-Deoxysugars With Isothiocyanates. Synthesis Of Cis-1,2-Fused Glycopyrano Heterocycles.
Cucurbituril: Supramolecular Perspectives For An Old Ligand
Condensation Of 2-Amino-2-Deoxysugars With Isothiocyanates. Synthesis Of Cis-1,2-Fused Glycopyrano Heterocycles.
Misconduct In Science [2]
Condensation Of 2-Amino-2-Deoxysugars With Isothiocyanates. Synthesis Of Cis-1,2-Fused Glycopyrano Heterocycles.
Misconduct In Science [2]
Structure Of Adducts Of 2-Arylaminothiazolines With Isocyanates And Isothiocyanates
Misconduct In Science [2]
Structure Of Adducts Of 2-Arylaminothiazolines With Isocyanates And Isothiocyanates
On The Mechanism Of Formation Of Glycofurano[2,1-D]-Imidazolidin-2-Ones. Reaction Of 2-Amino-2-Deoxyheptopyranoses With Isocyanates.
Structure Of Adducts Of 2-Arylaminothiazolines With Isocyanates And Isothiocyanates
On The Mechanism Of Formation Of Glycofurano[2,1-D]-Imidazolidin-2-Ones. Reaction Of 2-Amino-2-Deoxyheptopyranoses With Isocyanates.
The Reaction Of 2-Amino-2-Deoxyhexopyranoses With Isocyanates. Synthesis Of Ureas And Their Transformation Into Heterocyclic Derivatives.
On The Mechanism Of Formation Of Glycofurano[2,1-D]-Imidazolidin-2-Ones. Reaction Of 2-Amino-2-Deoxyheptopyranoses With Isocyanates.
The Reaction Of 2-Amino-2-Deoxyhexopyranoses With Isocyanates. Synthesis Of Ureas And Their Transformation Into Heterocyclic Derivatives.
A Novel Regio- And Highly Stereoselective Anomeric Deacetylation Of 2-Aminosugar Derivatives
The Reaction Of 2-Amino-2-Deoxyhexopyranoses With Isocyanates. Synthesis Of Ureas And Their Transformation Into Heterocyclic Derivatives.
A Novel Regio- And Highly Stereoselective Anomeric Deacetylation Of 2-Aminosugar Derivatives
Haloalkyl Isothiocyanates, Useful And Versatile Reagents In Heterocyclic Chemistry
A Novel Regio- And Highly Stereoselective Anomeric Deacetylation Of 2-Aminosugar Derivatives
Haloalkyl Isothiocyanates, Useful And Versatile Reagents In Heterocyclic Chemistry
Addition Of Organochromium Compounds To Aldehydes: The Nozaki-Hiyama Reaction
Haloalkyl Isothiocyanates, Useful And Versatile Reagents In Heterocyclic Chemistry
Addition Of Organochromium Compounds To Aldehydes: The Nozaki-Hiyama Reaction
Stereochemical Puzzle [2]
Addition Of Organochromium Compounds To Aldehydes: The Nozaki-Hiyama Reaction
Stereochemical Puzzle [2]
Diastereofacial Selectivity In Diels-Alder Reactions Of Chiral 1,2-Diaza-1,3-Butadienes From Carbohydrates
Stereochemical Puzzle [2]
Diastereofacial Selectivity In Diels-Alder Reactions Of Chiral 1,2-Diaza-1,3-Butadienes From Carbohydrates
Asymmetric Synthesis Of Α-Amino Acids From Carbohydrates As Chiral Templates
Diastereofacial Selectivity In Diels-Alder Reactions Of Chiral 1,2-Diaza-1,3-Butadienes From Carbohydrates
Asymmetric Synthesis Of Α-Amino Acids From Carbohydrates As Chiral Templates
Synthesis Of Sugar N-(2-Thiazolin-2-Yl)thioureas
Asymmetric Synthesis Of Α-Amino Acids From Carbohydrates As Chiral Templates
Synthesis Of Sugar N-(2-Thiazolin-2-Yl)thioureas
Synthesis Of 2-Alkyl(Aryl)amino-(3,4,6-Tri-O-Acetyl-1,2-Dideoxy-Α-D-Glucopyrano)[2,1-D]-2-Oxazolines And Ethyl 2-[3-Alkyl(Aryl)ureido]-2-Deoxy-Β-D-Glucopyranosides From Acetylated 2-[3-Alkyl(Aryl)ureido]-2-Deoxy-D-Glucopyranoses
Synthesis Of Sugar N-(2-Thiazolin-2-Yl)thioureas
Synthesis Of 2-Alkyl(Aryl)amino-(3,4,6-Tri-O-Acetyl-1,2-Dideoxy-Α-D-Glucopyrano)[2,1-D]-2-Oxazolines And Ethyl 2-[3-Alkyl(Aryl)ureido]-2-Deoxy-Β-D-Glucopyranosides From Acetylated 2-[3-Alkyl(Aryl)ureido]-2-Deoxy-D-Glucopyranoses
Synthesis Of Acylated Thioureylenedisaccharides
Synthesis Of 2-Alkyl(Aryl)amino-(3,4,6-Tri-O-Acetyl-1,2-Dideoxy-Α-D-Glucopyrano)[2,1-D]-2-Oxazolines And Ethyl 2-[3-Alkyl(Aryl)ureido]-2-Deoxy-Β-D-Glucopyranosides From Acetylated 2-[3-Alkyl(Aryl)ureido]-2-Deoxy-D-Glucopyranoses
Synthesis Of Acylated Thioureylenedisaccharides
Reaction Of Glycosylisothiocyanates With 2-Chloroethylamine. Synthesis And Structure Of N-Nucleoside Analogues
Synthesis Of Acylated Thioureylenedisaccharides
Reaction Of Glycosylisothiocyanates With 2-Chloroethylamine. Synthesis And Structure Of N-Nucleoside Analogues
Síntesis De Hidrobromuros De Glucopirano [2,1-D]-2-Tiazolinas
Reaction Of Glycosylisothiocyanates With 2-Chloroethylamine. Synthesis And Structure Of N-Nucleoside Analogues
Síntesis De Hidrobromuros De Glucopirano [2,1-D]-2-Tiazolinas
Beyond Conglomerates: A Minimalist Model Of The Viedma Deracemization Of Dl-Amino Acids
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