PUBLICACIÓN

Food Allergens: When Friends Become Foes—Caveats and Opportunities for Oral Immunotherapy Based on Deactivation Methods

Logo Open Access

ACCEDER A LA PUBLICACIÓN: Scopus Orcid

Gil M.V.; Fernandez-Rivera N.; Pastor-Vargas C.; Cintas P.

2023 Nutrients

Food Science (Q1), Nutrition and Dietetics (Q1)

JCR: 4.8

SJR: 1.301

CITAS

4

DOI

10.3390/nu15163650

EID

2-s2.0-85168730709

EISSN

2072-6643

AUTORES DE LA UEX

María Victoria Gil Álvarez
Pedro Cintas Moreno

OTRAS PUBLICACIONES DE INTERÉS

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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?
Synthesis And Antiproliferative Activity Of Peracetylated 2-Amino-1,2-Dideoxy-1-Nitro-D-Glycero-L-Manno And D-Glycero-D-Talo Heptitols
¿qué Sabemos De La Talidomida?
Synthesis And Antiproliferative Activity Of Peracetylated 2-Amino-1,2-Dideoxy-1-Nitro-D-Glycero-L-Manno And D-Glycero-D-Talo Heptitols
Green Chemical Synthesis And Click Reactions
Synthesis And Antiproliferative Activity Of Peracetylated 2-Amino-1,2-Dideoxy-1-Nitro-D-Glycero-L-Manno And D-Glycero-D-Talo Heptitols
Green Chemical Synthesis And Click Reactions
On Water Reactivity Between Carbohydrate-Derived Nitroalkenes And Furans
Green Chemical Synthesis And Click Reactions
On Water Reactivity Between Carbohydrate-Derived Nitroalkenes And Furans
Homochirogenesis And The Emergence Of Lifelike Structures
On Water Reactivity Between Carbohydrate-Derived Nitroalkenes And Furans
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
Phenolic Compounds And Antioxidant Capacity Of Virgin Olive Oil
Rethinking Aromaticity In H-Bonded Systems. Caveats For Transition Structures Involving Hydrogen Transfer And Π-Delocalization
Phenolic Compounds And Antioxidant Capacity Of Virgin Olive Oil
Expeditious 'on-Water' Cycloaddition Between N-Substituted Maleimides And Furans
Phenolic Compounds And Antioxidant Capacity Of Virgin Olive Oil
Expeditious 'on-Water' Cycloaddition Between N-Substituted Maleimides And Furans
Pseudo-Cyclic Structures Of Mono- And Di-Azaderivatives Of Malondialdehydes. Synthesis And Conformational Disentanglement By Computational Analyses
Expeditious 'on-Water' Cycloaddition Between N-Substituted Maleimides And Furans
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
Conjugated Nitrodienes. Synthesis And Reactivity
Non-Covalent Derivatization Of Aminosilanized Titanium Alloy Implants Silver-Enhanced Coating Of Antibacterial Organics
Conjugated Nitrodienes. Synthesis And Reactivity
Microwave-Assisted Synthesis Of N-Heterocycles In Medicinal Chemistry
Conjugated Nitrodienes. Synthesis And Reactivity
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
Classical Insecticides:past, Present And Future
Reticulated Pd(Ii)/cu(I) Cyclodextrin Complexes As Recyclable Green Catalyst For Sonogashira Alkynylation
Classical Insecticides:past, Present And Future
Combined Ultrasound- Microwave Technologies
Classical Insecticides:past, Present And Future
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
Discriminating Between Two Chiral Diastereoisomeric 7-Oxanitronorbornenes By Conventional X-Ray Powder Diffractometry
Power Ultrasound In Metal-Assisted Synthesis: From Classical Barbier-Like Reactions To Click Chemistry
Discriminating Between Two Chiral Diastereoisomeric 7-Oxanitronorbornenes By Conventional X-Ray Powder Diffractometry
Synthesis And Ring Opening Reactions Of 2-Glyco-1,4-Dimethyl-3-Nitro-7-Oxabicyclo[2.2.1]hept-5-Enes
Discriminating Between Two Chiral Diastereoisomeric 7-Oxanitronorbornenes By Conventional X-Ray Powder Diffractometry
Synthesis And Ring Opening Reactions Of 2-Glyco-1,4-Dimethyl-3-Nitro-7-Oxabicyclo[2.2.1]hept-5-Enes
Push-Pull 1,3-Thiazolium-5-Thiolates. Formation Via Concerted And Stepwise Pathways, And Theoretical Evaluation Of Nlo Properties
Synthesis And Ring Opening Reactions Of 2-Glyco-1,4-Dimethyl-3-Nitro-7-Oxabicyclo[2.2.1]hept-5-Enes
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
Laboratorio De Química: Generalidades Y Aspectos Básicos
Evolving Alchemy Into Chemistry: No Longer A Dichotomy
Laboratorio De Química: Generalidades Y Aspectos Básicos
Synthesis Of Chiral 2-Furyl And 3-Nitro-7-Oxabicyclo[2.2.1]heptane Derivatives From Sugars
Laboratorio De Química: Generalidades Y Aspectos Básicos
Synthesis Of Chiral 2-Furyl And 3-Nitro-7-Oxabicyclo[2.2.1]heptane Derivatives From Sugars
Dissecting Competitive Mechanisms: Thionation Vs. Cycloaddition In The Reaction Of Thioisomünchnones With Isothiocyanates Under Microwave Irradiation
Synthesis Of Chiral 2-Furyl And 3-Nitro-7-Oxabicyclo[2.2.1]heptane Derivatives From Sugars
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
New C-Aryl Alditols From Diels-Alder Adducts Of Sugar Nitroalkenes
Transition Metals In Radiation-Induced Reactions For Organic Synthesis: Applications Of Ultrasound
New C-Aryl Alditols From Diels-Alder Adducts Of Sugar Nitroalkenes
Unexpected Reactions: From (2s,3r)-2-(Endo-D-Galacto-Pentaacetoxypentyl)-1, 4-Dimethyl-3-Exo-Nitro-7-Oxabicyclo[2.2.1]hept-5-Ene To Chiral Cyclic Ethers
New C-Aryl Alditols From Diels-Alder Adducts Of Sugar Nitroalkenes
Unexpected Reactions: From (2s,3r)-2-(Endo-D-Galacto-Pentaacetoxypentyl)-1, 4-Dimethyl-3-Exo-Nitro-7-Oxabicyclo[2.2.1]hept-5-Ene To Chiral Cyclic Ethers
Pd-Catalyzed Reactions Promoted By Ultrasound And/or Microwave Irradiation
Unexpected Reactions: From (2s,3r)-2-(Endo-D-Galacto-Pentaacetoxypentyl)-1, 4-Dimethyl-3-Exo-Nitro-7-Oxabicyclo[2.2.1]hept-5-Ene To Chiral Cyclic Ethers
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
Adaptación Al Espacio Europeo De Educación Superior De La Asignatura Química Orgánica Básica En Los Estudios De Grado En Química En La Universidad De Extremadura.
Chirality And Chemical Processes: A Few Afterthoughts
Adaptación Al Espacio Europeo De Educación Superior De La Asignatura Química Orgánica Básica En Los Estudios De Grado En Química En La Universidad De Extremadura.
Adaptación De La Asignatura Química Orgánica Al Proceso De Convergencia Europea En Los Estudios Degrado En Química De La Universidad De Extremadura
Adaptación Al Espacio Europeo De Educación Superior De La Asignatura Química Orgánica Básica En Los Estudios De Grado En Química En La Universidad De Extremadura.
Adaptación De La Asignatura Química Orgánica Al Proceso De Convergencia Europea En Los Estudios Degrado En Química De La Universidad De Extremadura
Experiencias De La Implantación De Un Plan De Acción Tutorial
Adaptación De La Asignatura Química Orgánica Al Proceso De Convergencia Europea En Los Estudios Degrado En Química De La Universidad De Extremadura
Experiencias De La Implantación De Un Plan De Acción Tutorial
Click Chemistry - What's In A Name? Triazole Synthesis And Beyond
Experiencias De La Implantación De Un Plan De Acción Tutorial
Click Chemistry - What's In A Name? Triazole Synthesis And Beyond
Ultrasound-Induced Activation Of Metals: Principles And Applications In Organic Synthesis
Click Chemistry - What's In A Name? Triazole Synthesis And Beyond
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
Aplicación Al Suelo De Compost De Estiércol Bovino Como Fertilizante Orgánico: Experiencias Prácticas En Cultivos De Frutales Y De Viñedo
Extraction Of Flavourings From Natural Sources
Aplicación Al Suelo De Compost De Estiércol Bovino Como Fertilizante Orgánico: Experiencias Prácticas En Cultivos De Frutales Y De Viñedo
New Molecular Scaffolds: Synthesis Of (2r,3r)- And (2s,3s)-3-Nitro-7- Oxabicyclo[2.2.1]hept-5-Ene-2-Carbaldehyde From Furan
Aplicación Al Suelo De Compost De Estiércol Bovino Como Fertilizante Orgánico: Experiencias Prácticas En Cultivos De Frutales Y De Viñedo
New Molecular Scaffolds: Synthesis Of (2r,3r)- And (2s,3s)-3-Nitro-7- Oxabicyclo[2.2.1]hept-5-Ene-2-Carbaldehyde From Furan
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
New Molecular Scaffolds: Synthesis Of (2r,3r)- And (2s,3s)-3-Nitro-7- Oxabicyclo[2.2.1]hept-5-Ene-2-Carbaldehyde From Furan
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
Tandem Michael Addition And Intramolecular Aldol Cyclization Of 1,2-Dideoxy-1-Nitroheptitols Derived From Sugars
Sonochemical Cycloadditions In Ionic Liquids. Lessons From Model Cases Involving Common Dienes And Carbonyl Dienophiles
Tandem Michael Addition And Intramolecular Aldol Cyclization Of 1,2-Dideoxy-1-Nitroheptitols Derived From Sugars
New Trends In Pest Control: The Search For Greener Insecticides
Tandem Michael Addition And Intramolecular Aldol Cyclization Of 1,2-Dideoxy-1-Nitroheptitols Derived From Sugars
New Trends In Pest Control: The Search For Greener Insecticides
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 4: Absolute Stereochemistry Of Carbohydrate-Based Imidazolidine-2-Ones And 2-Thiones With Axial And Central Chirality
New Trends In Pest Control: The Search For Greener Insecticides
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
Cetyltrimethylammonium Hydroxide (Ctaoh) As A General, Ecofriendly Catalyst For The Formation Of Carbon-Carbon Bond Through Nitroalkanes
Chemistry And Luminescence
Cetyltrimethylammonium Hydroxide (Ctaoh) As A General, Ecofriendly Catalyst For The Formation Of Carbon-Carbon Bond Through Nitroalkanes
A New, One Pot Synthesis Of Alkylated Methyl Tri- And Tetracarboxylate Derivatives By Nitrolkanes
Cetyltrimethylammonium Hydroxide (Ctaoh) As A General, Ecofriendly Catalyst For The Formation Of Carbon-Carbon Bond Through Nitroalkanes
A New, One Pot Synthesis Of Alkylated Methyl Tri- And Tetracarboxylate Derivatives By Nitrolkanes
Erratum: One-Pot Synthesis Of Polyfunctionalized Α, Β-Unsaturated Nitriles From Nitroalkanes (Tetrahedron Letters (2003) 44 (9033-9034))
A New, One Pot Synthesis Of Alkylated Methyl Tri- And Tetracarboxylate Derivatives By Nitrolkanes
Erratum: One-Pot Synthesis Of Polyfunctionalized Α, Β-Unsaturated Nitriles From Nitroalkanes (Tetrahedron Letters (2003) 44 (9033-9034))
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
Erratum: One-Pot Synthesis Of Polyfunctionalized Α, Β-Unsaturated Nitriles From Nitroalkanes (Tetrahedron Letters (2003) 44 (9033-9034))
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))
One-Pot Synthesis Of Polyfunctionalized Α,β-Unsaturated Nitriles From Nitroalkanes
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))
One-Pot Synthesis Of Polyfunctionalized Α,β-Unsaturated Nitriles From Nitroalkanes
Δ-Nitroalkanols As Precursors For The One-Pot Synthesis Of Substituted Tetrahydrofurans
One-Pot Synthesis Of Polyfunctionalized Α,β-Unsaturated Nitriles From Nitroalkanes
Δ-Nitroalkanols As Precursors For The One-Pot Synthesis Of Substituted Tetrahydrofurans
Michael Addition Of Α-Nitro Ketones To Conjugated Enones Under Solventless Conditions Using Silica
Δ-Nitroalkanols As Precursors For The One-Pot Synthesis Of Substituted Tetrahydrofurans
Michael Addition Of Α-Nitro Ketones To Conjugated Enones Under Solventless Conditions Using Silica
The First Synthesis Of Pentadecyl 6-Hydroxydodecanoate A Novel Compound Isolated From The Leaves Of Artabotrys Odoratissimus
Michael Addition Of Α-Nitro Ketones To Conjugated Enones Under Solventless Conditions Using Silica
The First Synthesis Of Pentadecyl 6-Hydroxydodecanoate A Novel Compound Isolated From The Leaves Of Artabotrys Odoratissimus
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
The First Synthesis Of Pentadecyl 6-Hydroxydodecanoate A Novel Compound Isolated From The Leaves Of Artabotrys Odoratissimus
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
Preparation Of Enantiomerically Pure 4-Alkyl-5-Formyl-4-Nitrocyclohex-1-Enes From 5-Glyco-4-Nitrocyclohex-1-Enes
Sonochemical Effects In The Additions Of Furan To Masked Ortho-Benzoquinones
Preparation Of Enantiomerically Pure 4-Alkyl-5-Formyl-4-Nitrocyclohex-1-Enes From 5-Glyco-4-Nitrocyclohex-1-Enes
Reactions Of Hydroxylated Sodium Nitronates With Acetic Anhydride/pyridine
Preparation Of Enantiomerically Pure 4-Alkyl-5-Formyl-4-Nitrocyclohex-1-Enes From 5-Glyco-4-Nitrocyclohex-1-Enes
Reactions Of Hydroxylated Sodium Nitronates With Acetic Anhydride/pyridine
Studies On The Chemistry Of Sodium Nitronates And Nitronic Esters Derived From 5-Glyco-4-Nitro-1-Cyclohexenes
Reactions Of Hydroxylated Sodium Nitronates With Acetic Anhydride/pyridine
Studies On The Chemistry Of Sodium Nitronates And Nitronic Esters Derived From 5-Glyco-4-Nitro-1-Cyclohexenes
Michael Addition Of Nitroalkanes To Dimethyl Citraconate, With Dbu As Base: An Unexpected, One-Pot Synthesis Of Polyfunctionalized Carbonyl Derivatives
Studies On The Chemistry Of Sodium Nitronates And Nitronic Esters Derived From 5-Glyco-4-Nitro-1-Cyclohexenes
Michael Addition Of Nitroalkanes To Dimethyl Citraconate, With Dbu As Base: An Unexpected, One-Pot Synthesis Of Polyfunctionalized Carbonyl Derivatives
What Does Elementary Chirality Have To Do With Neutrinos?
Michael Addition Of Nitroalkanes To Dimethyl Citraconate, With Dbu As Base: An Unexpected, One-Pot Synthesis Of Polyfunctionalized Carbonyl Derivatives
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
Stereoselective Denitrohydrogenation Reactions Of 4-Alkyl-5-Glyco-4-Nitrocyclohex-1-Enes
Generation And Fate Of A Novel Homochiral Mesoionic Dipole: Synthesis Of C-Nucleoside Analogs
Stereoselective Denitrohydrogenation Reactions Of 4-Alkyl-5-Glyco-4-Nitrocyclohex-1-Enes
Nitrous Acid Elimination From 4-Alkyl-5-Formyl-4-Nitrocyclohex-1-Enes: Synthesis Of Mono And Bicyclic Benzene And Dihydrobenzene Derivatives
Stereoselective Denitrohydrogenation Reactions Of 4-Alkyl-5-Glyco-4-Nitrocyclohex-1-Enes
Nitrous Acid Elimination From 4-Alkyl-5-Formyl-4-Nitrocyclohex-1-Enes: Synthesis Of Mono And Bicyclic Benzene And Dihydrobenzene Derivatives
Synthesis Of Functionalized Nitrocyclohexene Derivatives From 2-Nitrocycloalkanones, Via Anionic Domino Reactions
Nitrous Acid Elimination From 4-Alkyl-5-Formyl-4-Nitrocyclohex-1-Enes: Synthesis Of Mono And Bicyclic Benzene And Dihydrobenzene Derivatives
Synthesis Of Functionalized Nitrocyclohexene Derivatives From 2-Nitrocycloalkanones, Via Anionic Domino Reactions
Stereoselective Synthesis Of (E)-4-Alkylidenecyclopent-2-En-1-Ones By A Tandem Ring Closure-Michael Addition-Elimination
Synthesis Of Functionalized Nitrocyclohexene Derivatives From 2-Nitrocycloalkanones, Via Anionic Domino Reactions
Stereoselective Synthesis Of (E)-4-Alkylidenecyclopent-2-En-1-Ones By A Tandem Ring Closure-Michael Addition-Elimination
Can We Predict The Conformational Preference Of Amides?
Stereoselective Synthesis Of (E)-4-Alkylidenecyclopent-2-En-1-Ones By A Tandem Ring Closure-Michael Addition-Elimination
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))
Procesos De Oxidación Avanzada: Aplicación A Compuestos Orgánicos En Disolución Acuosa
Erratum: Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone - Alkene Cycloaddition Reaction (European Journal Of Organic Chemistry (2001) (2135-2144))
Procesos De Oxidación Avanzada: Aplicación A Compuestos Orgánicos En Disolución Acuosa
Benzoxocin, Benzoxepin And Benzofuran Frameworks From 5-Glyco-4-Nitrocyclohex-1-Enes Through Nef Reaction And Intramolecular Cyclization
Procesos De Oxidación Avanzada: Aplicación A Compuestos Orgánicos En Disolución Acuosa
Benzoxocin, Benzoxepin And Benzofuran Frameworks From 5-Glyco-4-Nitrocyclohex-1-Enes Through Nef Reaction And Intramolecular Cyclization
Unexpected Transformations: From 5-Glyco-4-Nitrocyclohexenes To Bicyclic [3.3.1] Oximes Through Isoxazoline N-Oxides
Benzoxocin, Benzoxepin And Benzofuran Frameworks From 5-Glyco-4-Nitrocyclohex-1-Enes Through Nef Reaction And Intramolecular Cyclization
Unexpected Transformations: From 5-Glyco-4-Nitrocyclohexenes To Bicyclic [3.3.1] Oximes Through Isoxazoline N-Oxides
Reactions Of 2-Amino-2-Thiazolines With Isocyanates And Isothiocyanates. Chemical And Computational Studies On The Regioselectivity, Adduct Rearrangement, And Mechanistic Pathways
Unexpected Transformations: From 5-Glyco-4-Nitrocyclohexenes To Bicyclic [3.3.1] Oximes Through Isoxazoline N-Oxides
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
Importancia De Los Compuestos Fenólicos En Los Vinos
Absolute Asymmetric Synthesis Under Physical Fields: Facts And Fictions
Importancia De Los Compuestos Fenólicos En Los Vinos
Stereoselective Michael Addition Reactions Of 5-Glyco-4-Nitrocyclohex- 1-Enes
Importancia De Los Compuestos Fenólicos En Los Vinos
Stereoselective Michael Addition Reactions Of 5-Glyco-4-Nitrocyclohex- 1-Enes
Reactions Of Thioamides With Metal Carboxylates In Organic Media
Stereoselective Michael Addition Reactions Of 5-Glyco-4-Nitrocyclohex- 1-Enes
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
Unraveling The Conglomeratic Nature Of Methanol Clusters Adsorbed On Graphene Surfaces. Insights From Molecular Dynamics Simulations
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