PUBLICACIÓN

Schiff bases from TRIS and formylpyridines: Structure and mechanistic rationale aided by DFT calculations

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ACCEDER A LA PUBLICACIÓN: Scopus Orcid

Martinez R.F., Avalos M., Babiano R., Cintas P., Jimenez J.L., Light M.E., Palacios J.C., Perez E.M.S.

2010 EUROPEAN JOURNAL OF ORGANIC CHEMISTRY

Organic Chemistry (Q1), Physical and Theoretical Chemistry (Q1)

JCR: 3.206

SJR: 1.615

CITAS

8

DOI

10.1002/ejoc.201000922

EID

2-s2.0-78249244122

ISSN

1434-193X

EISSN

1099-0690

BIBTEX

@article{RID:1002140712918-26, title = {Schiff Bases from TRIS and Formylpyridines: Structure and Mechanistic Rationale Aided by DFT Calculations}, journal = {European Journal of Organic Chemistry}, year = {2010}, author = {Fernando Martinez, R. and Avalos, Martin and Babiano, Reyes and Cintas, Pedro and Jimenez, Jose L. and Light, Mark E. and Palacios, Juan C. and Perez, Esther M. S.}, number = {32}, pages = {6224-6232} }

AUTORES DE LA UEX

Pedro Cintas Moreno
Rafael Fernando Martínez Vázquez
Esther María Pérez Rosa

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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
Nine Of 16 Stereoisomeric Polyhydroxylated Proline Amides Are Potent Β-N-Acetylhexosaminidase Inhibitors
Rethinking Aromaticity In H-Bonded Systems. Caveats For Transition Structures Involving Hydrogen Transfer And Π-Delocalization
Nine Of 16 Stereoisomeric Polyhydroxylated Proline Amides Are Potent Β-N-Acetylhexosaminidase Inhibitors
Carbohydrate Derived Bicyclic Azetidin-3-Ones As Scaffolds For Highly Functionalized Azetidines
Nine Of 16 Stereoisomeric Polyhydroxylated Proline Amides Are Potent Β-N-Acetylhexosaminidase Inhibitors
Carbohydrate Derived Bicyclic Azetidin-3-Ones As Scaffolds For Highly Functionalized Azetidines
Short And Sweet: D-Glucose To L-Glucose And L-Glucuronic Acid
Carbohydrate Derived Bicyclic Azetidin-3-Ones As Scaffolds For Highly Functionalized Azetidines
Short And Sweet: D-Glucose To L-Glucose And L-Glucuronic Acid
Synthesis Of The Enantiomers Of Xylnac And Lyxnac: Comparison Of Β-N-Acetylhexosaminidase Inhibition By The 8 Stereoisomers Of 2-N-Acetylamino-1,2,4-Trideoxy-1,4-Iminopentitols
Short And Sweet: D-Glucose To L-Glucose And L-Glucuronic Acid
Synthesis Of The Enantiomers Of Xylnac And Lyxnac: Comparison Of Β-N-Acetylhexosaminidase Inhibition By The 8 Stereoisomers Of 2-N-Acetylamino-1,2,4-Trideoxy-1,4-Iminopentitols
Kurz Und Knapp:l-Glucose Undl-Glucuronsäure Ausd-Glucose
Synthesis Of The Enantiomers Of Xylnac And Lyxnac: Comparison Of Β-N-Acetylhexosaminidase Inhibition By The 8 Stereoisomers Of 2-N-Acetylamino-1,2,4-Trideoxy-1,4-Iminopentitols
Kurz Und Knapp:l-Glucose Undl-Glucuronsäure Ausd-Glucose
Pseudo-Cyclic Structures Of Mono- And Di-Azaderivatives Of Malondialdehydes. Synthesis And Conformational Disentanglement By Computational Analyses
Kurz Und Knapp:l-Glucose Undl-Glucuronsäure Ausd-Glucose
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
Rhodamine And Bodipy Chemodosimeters And Chemosensors For The Detection Of Hg2+, Based On Fluorescence Enhancement Effects
Non-Covalent Derivatization Of Aminosilanized Titanium Alloy Implants Silver-Enhanced Coating Of Antibacterial Organics
Rhodamine And Bodipy Chemodosimeters And Chemosensors For The Detection Of Hg2+, Based On Fluorescence Enhancement Effects
Photoinduced Electron Transfer Fluorometric Hg(Ii) Chemosensor Based On A Bodipy Armed With A Tetrapod Receptor
Rhodamine And Bodipy Chemodosimeters And Chemosensors For The Detection Of Hg2+, Based On Fluorescence Enhancement Effects
Photoinduced Electron Transfer Fluorometric Hg(Ii) Chemosensor Based On A Bodipy Armed With A Tetrapod Receptor
(3r,4s,5r,6r,7s)-3,4,5,7-Tetrahydroxyconidine, An Azetidine Analogue Of 6,7-Diepicastanospermine And A Conformationally Constrained D- Deoxyaltronojirimycin, From L-Arabinose
Photoinduced Electron Transfer Fluorometric Hg(Ii) Chemosensor Based On A Bodipy Armed With A Tetrapod Receptor
(3r,4s,5r,6r,7s)-3,4,5,7-Tetrahydroxyconidine, An Azetidine Analogue Of 6,7-Diepicastanospermine And A Conformationally Constrained D- Deoxyaltronojirimycin, From L-Arabinose
C-Branched Iminosugars: Α-Glucosidase Inhibition By Enantiomers Of Isodmdp, Isodgdp, And Isodab- L -Isodmdp Compared To Miglitol And Miglustat
(3r,4s,5r,6r,7s)-3,4,5,7-Tetrahydroxyconidine, An Azetidine Analogue Of 6,7-Diepicastanospermine And A Conformationally Constrained D- Deoxyaltronojirimycin, From L-Arabinose
C-Branched Iminosugars: Α-Glucosidase Inhibition By Enantiomers Of Isodmdp, Isodgdp, And Isodab- L -Isodmdp Compared To Miglitol And Miglustat
Microwave-Assisted Synthesis Of N-Heterocycles In Medicinal Chemistry
C-Branched Iminosugars: Α-Glucosidase Inhibition By Enantiomers Of Isodmdp, Isodgdp, And Isodab- L -Isodmdp Compared To Miglitol And Miglustat
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
Azetidine Iminosugars From The Cyclization Of 3,5-Di- O -Triflates Of Α-Furanosides And Of 2,4-Di- O -Triflates Of Β-Pyranosides Derived From Glucose
Complementary And Synergic Effects Of Microwaves And Ultrasound In Metal-Assisted Synthesis
Azetidine Iminosugars From The Cyclization Of 3,5-Di- O -Triflates Of Α-Furanosides And Of 2,4-Di- O -Triflates Of Β-Pyranosides Derived From Glucose
N-(2-Carboxyethyl)-2,5-Dideoxy-2,5-Imino-D-Mannonic Acid [(3r,4r,5r)-1-(2-Carboxyethyl)-3,4-Dihydroxy-5-Hydroxymethyl-L-Proline]
Azetidine Iminosugars From The Cyclization Of 3,5-Di- O -Triflates Of Α-Furanosides And Of 2,4-Di- O -Triflates Of Β-Pyranosides Derived From Glucose
N-(2-Carboxyethyl)-2,5-Dideoxy-2,5-Imino-D-Mannonic Acid [(3r,4r,5r)-1-(2-Carboxyethyl)-3,4-Dihydroxy-5-Hydroxymethyl-L-Proline]
Glycosidase Inhibition By All 10 Stereoisomeric 2,5-Dideoxy-2,5- Iminohexitols Prepared From The Enantiomers Of Glucuronolactone
N-(2-Carboxyethyl)-2,5-Dideoxy-2,5-Imino-D-Mannonic Acid [(3r,4r,5r)-1-(2-Carboxyethyl)-3,4-Dihydroxy-5-Hydroxymethyl-L-Proline]
Glycosidase Inhibition By All 10 Stereoisomeric 2,5-Dideoxy-2,5- Iminohexitols Prepared From The Enantiomers Of Glucuronolactone
Synthesis From D-Altrose Of (5 R,6 R,7 R,8 S)-5,7-Dihydroxy-8- Hydroxymethylconidine And 2,4-Dideoxy-2,4-Imino-D-Glucitol, Azetidine Analogues Of Swainsonine And 1,4-Dideoxy-1,4-Imino-D-Mannitol
Glycosidase Inhibition By All 10 Stereoisomeric 2,5-Dideoxy-2,5- Iminohexitols Prepared From The Enantiomers Of Glucuronolactone
Synthesis From D-Altrose Of (5 R,6 R,7 R,8 S)-5,7-Dihydroxy-8- Hydroxymethylconidine And 2,4-Dideoxy-2,4-Imino-D-Glucitol, Azetidine Analogues Of Swainsonine And 1,4-Dideoxy-1,4-Imino-D-Mannitol
On The Physical Basis Of Asymmetry And Homochirality
Synthesis From D-Altrose Of (5 R,6 R,7 R,8 S)-5,7-Dihydroxy-8- Hydroxymethylconidine And 2,4-Dideoxy-2,4-Imino-D-Glucitol, Azetidine Analogues Of Swainsonine And 1,4-Dideoxy-1,4-Imino-D-Mannitol
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
Breed As Risk Factor For Oesophageal Foreign Bodies
Power Ultrasound In Metal-Assisted Synthesis: From Classical Barbier-Like Reactions To Click Chemistry
Breed As Risk Factor For Oesophageal Foreign Bodies
Push-Pull 1,3-Thiazolium-5-Thiolates. Formation Via Concerted And Stepwise Pathways, And Theoretical Evaluation Of Nlo Properties
Breed As Risk Factor For Oesophageal Foreign Bodies
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
Morphometry Of The Abdominal Esophagus And Stomach Of The Rabbit. Laparoscopyc Surgery Applications
Evolving Alchemy Into Chemistry: No Longer A Dichotomy
Morphometry Of The Abdominal Esophagus And Stomach Of The Rabbit. Laparoscopyc Surgery Applications
Dissecting Competitive Mechanisms: Thionation Vs. Cycloaddition In The Reaction Of Thioisomünchnones With Isothiocyanates Under Microwave Irradiation
Morphometry Of The Abdominal Esophagus And Stomach Of The Rabbit. Laparoscopyc Surgery Applications
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
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
Ultrasound-Induced Activation Of Metals: Principles And Applications In Organic Synthesis
Adaptación De La Asignatura Química Orgánica Al Proceso De Convergencia Europea En Los Estudios Degrado En Química De La Universidad De Extremadura
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
Enhanced Diels-Alder Reactions: On The Role Of Mineral Catalysts And Microwave Irradiation In Ionic Liquids As Recyclable Media
Extraction Of Flavourings From Natural Sources
Enhanced Diels-Alder Reactions: On The Role Of Mineral Catalysts And Microwave Irradiation In Ionic Liquids As Recyclable Media
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
Enhanced Diels-Alder Reactions: On The Role Of Mineral Catalysts And Microwave Irradiation In Ionic Liquids As Recyclable Media
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
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Chemistry And Luminescence
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
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))
Tiletamine-Zolazepam Anesthesia In Horses: Repeated Dose Versus Continuous Infusion
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))
Tiletamine-Zolazepam Anesthesia In Horses: Repeated Dose Versus Continuous Infusion
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Tiletamine-Zolazepam Anesthesia In Horses: Repeated Dose Versus Continuous Infusion
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
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 Olefinst
Generation And Fate Of A Novel Homochiral Mesoionic Dipole: Synthesis Of C-Nucleoside Analogs
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 Olefinst
Can We Predict The Conformational Preference Of Amides?
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 Olefinst
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))
Carbohydrate-Derived Dienes For Intramolecular And Asymmetric Diels-Alder Reactions
Erratum: Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone - Alkene Cycloaddition Reaction (European Journal Of Organic Chemistry (2001) (2135-2144))
Carbohydrate-Derived Dienes For Intramolecular And Asymmetric Diels-Alder Reactions
Reactions Of 2-Amino-2-Thiazolines With Isocyanates And Isothiocyanates. Chemical And Computational Studies On The Regioselectivity, Adduct Rearrangement, And Mechanistic Pathways
Carbohydrate-Derived Dienes For Intramolecular And Asymmetric Diels-Alder Reactions
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
Preparation Of Riboflavin 4',5'-Cyclic Phosphate By Incubation Of Flavin-Adenine Dinucleotide With Mn2+ In The Absence Of Riboflavin 5'- Phosphate Cyclase
Understanding Diastereofacial Selection In Carbohydrate-Based Domino Cycloadditions: Semiempirical And Dft Calculations
Preparation Of Riboflavin 4',5'-Cyclic Phosphate By Incubation Of Flavin-Adenine Dinucleotide With Mn2+ In The Absence Of Riboflavin 5'- Phosphate Cyclase
Expeditious Formation Of 1,2,4-Triazine Derivatives Via A Thioisomunchnone Cycloaddition Reaction
Preparation Of Riboflavin 4',5'-Cyclic Phosphate By Incubation Of Flavin-Adenine Dinucleotide With Mn2+ In The Absence Of Riboflavin 5'- Phosphate Cyclase
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
Asymmetric Tandem Reactions Based On Nitroalkenes: A One-Pot Construction Of Functionalized Chiral Bicycles By A Three-Component Reaction
Absolute Asymmetric Synthesis Under Physical Fields: Facts And Fictions
Asymmetric Tandem Reactions Based On Nitroalkenes: A One-Pot Construction Of Functionalized Chiral Bicycles By A Three-Component Reaction
Enzymic Formation Of Riboflavin 4′,5′-Cyclic Phosphate From Fad: Evidence For A Specific Low-Km Fmn Cyclase In Rat Liver
Asymmetric Tandem Reactions Based On Nitroalkenes: A One-Pot Construction Of Functionalized Chiral Bicycles By A Three-Component Reaction
Enzymic Formation Of Riboflavin 4′,5′-Cyclic Phosphate From Fad: Evidence For A Specific Low-Km Fmn Cyclase In Rat Liver
Glycine-Enhanced Inhibition Of Rat Liver Nucleotide Pyrophosphatase/phosphodiesterase-I By Edta: A Full Account Of The Reported Inhibition By Commercial Preparations Of Acidic Fibroblast Growth Factor (Fgf-1)
Enzymic Formation Of Riboflavin 4′,5′-Cyclic Phosphate From Fad: Evidence For A Specific Low-Km Fmn Cyclase In Rat Liver
Glycine-Enhanced Inhibition Of Rat Liver Nucleotide Pyrophosphatase/phosphodiesterase-I By Edta: A Full Account Of The Reported Inhibition By Commercial Preparations Of Acidic Fibroblast Growth Factor (Fgf-1)
Reactions Of Thioamides With Metal Carboxylates In Organic Media
Glycine-Enhanced Inhibition Of Rat Liver Nucleotide Pyrophosphatase/phosphodiesterase-I By Edta: A Full Account Of The Reported Inhibition By Commercial Preparations Of Acidic Fibroblast Growth Factor (Fgf-1)
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
Identification Of Rat Liver Glucose-3-Phosphatase As An Inositol Monophosphatase Inhibited By Lithium
Nonlinear Stereochemical Effects In Asymmetric Reactions
Identification Of Rat Liver Glucose-3-Phosphatase As An Inositol Monophosphatase Inhibited By Lithium
Isolation Of New Nonconditional Saccharomyces Cerevisiae Mutants Defective In Asparagine-Linked Glycosylation
Identification Of Rat Liver Glucose-3-Phosphatase As An Inositol Monophosphatase Inhibited By Lithium
Isolation Of New Nonconditional Saccharomyces Cerevisiae Mutants Defective In Asparagine-Linked Glycosylation
Nmr Studies And Semiempirical Calculations On The Structure Of Glycoamidines
Isolation Of New Nonconditional Saccharomyces Cerevisiae Mutants Defective In Asparagine-Linked Glycosylation
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.
Reaction Of Thioamides With Silver Carboxylates In Aprotic Media. A Nucleophilic Approach To The Synthesis Of Imides, Amides, And Nitriles
Condensation Of 2-Amino-2-Deoxysugars With Isothiocyanates. Synthesis Of Cis-1,2-Fused Glycopyrano Heterocycles.
Reaction Of Thioamides With Silver Carboxylates In Aprotic Media. A Nucleophilic Approach To The Synthesis Of Imides, Amides, And Nitriles
Misconduct In Science [2]
Reaction Of Thioamides With Silver Carboxylates In Aprotic Media. A Nucleophilic Approach To The Synthesis Of Imides, Amides, And Nitriles
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
Diastereoselective Synthesis Of Chiral Thiiranes By 1,3-Dipolar Cycloaddition Of Imidazo[2,1-B]thiazolium-4-Olate Systems With Aromatic Aldehydes
A Novel Regio- And Highly Stereoselective Anomeric Deacetylation Of 2-Aminosugar Derivatives
Diastereoselective Synthesis Of Chiral Thiiranes By 1,3-Dipolar Cycloaddition Of Imidazo[2,1-B]thiazolium-4-Olate Systems With Aromatic Aldehydes
Alcohol Esterification Reactions And Mechanisms Of Snake Venom 5′‐nucleotide Phosphodiesterase
Diastereoselective Synthesis Of Chiral Thiiranes By 1,3-Dipolar Cycloaddition Of Imidazo[2,1-B]thiazolium-4-Olate Systems With Aromatic Aldehydes
Alcohol Esterification Reactions And Mechanisms Of Snake Venom 5′‐nucleotide Phosphodiesterase
Haloalkyl Isothiocyanates, Useful And Versatile Reagents In Heterocyclic Chemistry
Alcohol Esterification Reactions And Mechanisms Of Snake Venom 5′‐nucleotide Phosphodiesterase
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
Nmr Studies Of Sugar Amides And Thioamides
Addition Of Organochromium Compounds To Aldehydes: The Nozaki-Hiyama Reaction
Nmr Studies Of Sugar Amides And Thioamides
A New Synthesis Of 6-Oxopyrimidinium-4-Olates. Theoretical Study Of The Regioselective Cycloaddition Of Arylisocyanates With A 1,3-Thiazolium-4-Olate System
Nmr Studies Of Sugar Amides And Thioamides
A New Synthesis Of 6-Oxopyrimidinium-4-Olates. Theoretical Study Of The Regioselective Cycloaddition Of Arylisocyanates With A 1,3-Thiazolium-4-Olate System
Stereochemical Puzzle [2]
A New Synthesis Of 6-Oxopyrimidinium-4-Olates. Theoretical Study Of The Regioselective Cycloaddition Of Arylisocyanates With A 1,3-Thiazolium-4-Olate System
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 And Reactivity Toward Acetylenic Dipolarophiles Of Imidazo[2,1-B]thiazolium-3-Olate Systems
Asymmetric Synthesis Of Α-Amino Acids From Carbohydrates As Chiral Templates
Synthesis And Reactivity Toward Acetylenic Dipolarophiles Of Imidazo[2,1-B]thiazolium-3-Olate Systems
Methanol Esterification Reactions Catalyzed By Snake Venom And Bovine Intestinal 5′‐nucleotide Phosphodiesterases: Formation Of Nucleoside 5′‐monophosphate Methyl Esters From Guanosine 5′‐triphosphate And Other Nucleoside 5′‐polyphosphates
Synthesis And Reactivity Toward Acetylenic Dipolarophiles Of Imidazo[2,1-B]thiazolium-3-Olate Systems
Methanol Esterification Reactions Catalyzed By Snake Venom And Bovine Intestinal 5′‐nucleotide Phosphodiesterases: Formation Of Nucleoside 5′‐monophosphate Methyl Esters From Guanosine 5′‐triphosphate And Other Nucleoside 5′‐polyphosphates
Synthesis Of Sugar N-(2-Thiazolin-2-Yl)thioureas
Methanol Esterification Reactions Catalyzed By Snake Venom And Bovine Intestinal 5′‐nucleotide Phosphodiesterases: Formation Of Nucleoside 5′‐monophosphate Methyl Esters From Guanosine 5′‐triphosphate And Other Nucleoside 5′‐polyphosphates
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
Synthesis Of N,n′-Bis(Aryl)-N-(2-Thiazolin-2-Yl)thioureas
Reaction Of Glycosylisothiocyanates With 2-Chloroethylamine. Synthesis And Structure Of N-Nucleoside Analogues
Synthesis Of N,n′-Bis(Aryl)-N-(2-Thiazolin-2-Yl)thioureas
Reduction Of Isothiocyanates To Thioformamides With Tri-N-Butyltin Hydride
Synthesis Of N,n′-Bis(Aryl)-N-(2-Thiazolin-2-Yl)thioureas
Reduction Of Isothiocyanates To Thioformamides With Tri-N-Butyltin Hydride
Synthesis Of Glycofurano[2,1-D]imidazolidin-2-Ones
Reduction Of Isothiocyanates To Thioformamides With Tri-N-Butyltin Hydride
Synthesis Of Glycofurano[2,1-D]imidazolidin-2-Ones
An Efficient And Regioselective Synthesis Of Acyclic C-Nucleosides From Mesoionic Compounds
Synthesis Of Glycofurano[2,1-D]imidazolidin-2-Ones
An Efficient And Regioselective Synthesis Of Acyclic C-Nucleosides From Mesoionic Compounds
Reaction Of Glycosylisothiocyanates With 2-Chloroethylamine
An Efficient And Regioselective Synthesis Of Acyclic C-Nucleosides From Mesoionic Compounds
Reaction Of Glycosylisothiocyanates With 2-Chloroethylamine
Oxidation Of Enamines Derived From Sugars
Reaction Of Glycosylisothiocyanates With 2-Chloroethylamine
Oxidation Of Enamines Derived From Sugars
Syntheses Of Partially Protected D-Galactopyranosylthioureas: New D-Galactopyranosylimidazoline-2-Thiones And D-Galactopyranosylaminothiazoles
Oxidation Of Enamines Derived From Sugars
Syntheses Of Partially Protected D-Galactopyranosylthioureas: New D-Galactopyranosylimidazoline-2-Thiones And D-Galactopyranosylaminothiazoles
Regioselective Benzoylations Of Glycopyranosylamines: Synthesis Of Partially Protected Glycopyranosyl Isothiocyanates
Syntheses Of Partially Protected D-Galactopyranosylthioureas: New D-Galactopyranosylimidazoline-2-Thiones And D-Galactopyranosylaminothiazoles
Regioselective Benzoylations Of Glycopyranosylamines: Synthesis Of Partially Protected Glycopyranosyl Isothiocyanates
Syntheses Of D-Ribosylamines, D-Ribopyranosyl Isothiocyanates, And D-Ribopyranosylthioureas, And Their Transformations Into Heterocyclic Compounds
Regioselective Benzoylations Of Glycopyranosylamines: Synthesis Of Partially Protected Glycopyranosyl Isothiocyanates
Syntheses Of D-Ribosylamines, D-Ribopyranosyl Isothiocyanates, And D-Ribopyranosylthioureas, And Their Transformations Into Heterocyclic Compounds
Protonation Study Of Biological Bases Of Dna
Syntheses Of D-Ribosylamines, D-Ribopyranosyl Isothiocyanates, And D-Ribopyranosylthioureas, And Their Transformations Into Heterocyclic Compounds
Protonation Study Of Biological Bases Of Dna
A Discussion Of The Hammett Acidity Function. Study Of Some Weak Bases
Protonation Study Of Biological Bases Of Dna
A Discussion Of The Hammett Acidity Function. Study Of Some Weak Bases
Síntesis De Hidrobromuros De Glucopirano [2,1-D]-2-Tiazolinas
A Discussion Of The Hammett Acidity Function. Study Of Some Weak Bases
Síntesis De Hidrobromuros De Glucopirano [2,1-D]-2-Tiazolinas
Acylation Of Glycofurano[2,1-D]imidazolidine-2-Thiones: A Structural Revision
Síntesis De Hidrobromuros De Glucopirano [2,1-D]-2-Tiazolinas
Acylation Of Glycofurano[2,1-D]imidazolidine-2-Thiones: A Structural Revision
Facile Preparation Of C-Glycosylbarbiturates And C-Glycosylbarbituric Acids
Acylation Of Glycofurano[2,1-D]imidazolidine-2-Thiones: A Structural Revision
Facile Preparation Of C-Glycosylbarbiturates And C-Glycosylbarbituric Acids
Synthesis Of 1,3,4,6-Tetra-O-Acetyl-2-[3-Alkyl-(Aryl)-Thioreido]-2-Deoxy-Α-D-Glucopyranoses And Their Transformation Into 2-Alkyl(Aryl)amino-(1,2-Dideoxy-Α-D-Glucopyrano)[2,1-D]-2-Thiazolines
Facile Preparation Of C-Glycosylbarbiturates And C-Glycosylbarbituric Acids
Synthesis Of 1,3,4,6-Tetra-O-Acetyl-2-[3-Alkyl-(Aryl)-Thioreido]-2-Deoxy-Α-D-Glucopyranoses And Their Transformation Into 2-Alkyl(Aryl)amino-(1,2-Dideoxy-Α-D-Glucopyrano)[2,1-D]-2-Thiazolines
A New Method For The Preparation Of Acylated Glycosylamines And Their Transformations Into Glycosyl Isothiocyanates And N,n′-Diglycosylthioureas
Synthesis Of 1,3,4,6-Tetra-O-Acetyl-2-[3-Alkyl-(Aryl)-Thioreido]-2-Deoxy-Α-D-Glucopyranoses And Their Transformation Into 2-Alkyl(Aryl)amino-(1,2-Dideoxy-Α-D-Glucopyrano)[2,1-D]-2-Thiazolines
A New Method For The Preparation Of Acylated Glycosylamines And Their Transformations Into Glycosyl Isothiocyanates And N,n′-Diglycosylthioureas
3-Alquil-1-Aril(Glicoheptofurano)imidazolidina-2-Tionas Derivadas De Nuevas 2-(Alquilamino)-2-Desoxi-Heptosas De Configuración D-Glicero-L-Gluco, D-Glicero-L-Mano, D-Glicero-D-Gulo Y D-Glicero-D-Ido
A New Method For The Preparation Of Acylated Glycosylamines And Their Transformations Into Glycosyl Isothiocyanates And N,n′-Diglycosylthioureas
3-Alquil-1-Aril(Glicoheptofurano)imidazolidina-2-Tionas Derivadas De Nuevas 2-(Alquilamino)-2-Desoxi-Heptosas De Configuración D-Glicero-L-Gluco, D-Glicero-L-Mano, D-Glicero-D-Gulo Y D-Glicero-D-Ido
Preparación Del Hidrocloruro De 2-Amino-2-Desoxi-D-Glicero-D-Altro-Heptosa A Partir De D-Alosa
3-Alquil-1-Aril(Glicoheptofurano)imidazolidina-2-Tionas Derivadas De Nuevas 2-(Alquilamino)-2-Desoxi-Heptosas De Configuración D-Glicero-L-Gluco, D-Glicero-L-Mano, D-Glicero-D-Gulo Y D-Glicero-D-Ido
Preparación Del Hidrocloruro De 2-Amino-2-Desoxi-D-Glicero-D-Altro-Heptosa A Partir De D-Alosa
New Acyclic-Sugar C-Nucleoside Analogs. Synthesis Of 2-(Alditol-1-Yl)-1-Alkyl-4,5,6,7-Tetrahydroindol-4-Ones
Preparación Del Hidrocloruro De 2-Amino-2-Desoxi-D-Glicero-D-Altro-Heptosa A Partir De D-Alosa
New Acyclic-Sugar C-Nucleoside Analogs. Synthesis Of 2-(Alditol-1-Yl)-1-Alkyl-4,5,6,7-Tetrahydroindol-4-Ones
Synthesis Of D-Ribo-C-Nucleoside Analogues By Dehydration Of New D-Allo-Pentitol-1-Yl Heterocycles
New Acyclic-Sugar C-Nucleoside Analogs. Synthesis Of 2-(Alditol-1-Yl)-1-Alkyl-4,5,6,7-Tetrahydroindol-4-Ones
Synthesis Of D-Ribo-C-Nucleoside Analogues By Dehydration Of New D-Allo-Pentitol-1-Yl Heterocycles
Limitations Of The Aminonitrile Synthesis. New Products From D-Glucose, D-Galactose, And D-Mannose
Synthesis Of D-Ribo-C-Nucleoside Analogues By Dehydration Of New D-Allo-Pentitol-1-Yl Heterocycles
Limitations Of The Aminonitrile Synthesis. New Products From D-Glucose, D-Galactose, And D-Mannose
Tioureas Derivadas De Carbohidratos. V. Isotiocianato Y Tioureas Derivadas De La 2-Amino-2-Desoxi-D-Glicero-Α-L-Gluco-Heptopiranosa
Limitations Of The Aminonitrile Synthesis. New Products From D-Glucose, D-Galactose, And D-Mannose
Tioureas Derivadas De Carbohidratos. V. Isotiocianato Y Tioureas Derivadas De La 2-Amino-2-Desoxi-D-Glicero-Α-L-Gluco-Heptopiranosa
Acyclic-Sugar Pyrrole C-Nucleoside-Analogs Derived From 2-(Alkylamino)-2-Deoxyaldoses
Tioureas Derivadas De Carbohidratos. V. Isotiocianato Y Tioureas Derivadas De La 2-Amino-2-Desoxi-D-Glicero-Α-L-Gluco-Heptopiranosa
Acyclic-Sugar Pyrrole C-Nucleoside-Analogs Derived From 2-(Alkylamino)-2-Deoxyaldoses
1-Aryl(Glycofurano)imidazolidine-2-Thiones Derived From New 2-(Alkylamino)-2-Deoxyheptoses Having D-Glycero- D-Galacto And D-Glycero-D-Talo Configurations
Acyclic-Sugar Pyrrole C-Nucleoside-Analogs Derived From 2-(Alkylamino)-2-Deoxyaldoses
1-Aryl(Glycofurano)imidazolidine-2-Thiones Derived From New 2-(Alkylamino)-2-Deoxyheptoses Having D-Glycero- D-Galacto And D-Glycero-D-Talo Configurations
Synthesis Of 1-Aryl-(Glycofurano)imidazolidine-2-Thiones From New 2-(Alkylamino)-2-Deoxyhexoses
1-Aryl(Glycofurano)imidazolidine-2-Thiones Derived From New 2-(Alkylamino)-2-Deoxyheptoses Having D-Glycero- D-Galacto And D-Glycero-D-Talo Configurations
Synthesis Of 1-Aryl-(Glycofurano)imidazolidine-2-Thiones From New 2-(Alkylamino)-2-Deoxyhexoses
A Facile Synthesis Of C-Glycosylbarbiturates
Synthesis Of 1-Aryl-(Glycofurano)imidazolidine-2-Thiones From New 2-(Alkylamino)-2-Deoxyhexoses
A Facile Synthesis Of C-Glycosylbarbiturates
Syntheses Of 2-Amino- And 2-(Benzylamino)-2-Deoxyheptonic Acids
A Facile Synthesis Of C-Glycosylbarbiturates
Syntheses Of 2-Amino- And 2-(Benzylamino)-2-Deoxyheptonic Acids
Preparation Of C-Nucleosides By Dehydration Of Pentahydroxypentyl-Heterocycles: Steric Course And Mechanism
Syntheses Of 2-Amino- And 2-(Benzylamino)-2-Deoxyheptonic Acids
Preparation Of C-Nucleosides By Dehydration Of Pentahydroxypentyl-Heterocycles: Steric Course And Mechanism
Catalytic Screening For 1,2-Diol Protection: A Saccharose-Derived Hydrothermal Carbon Showcases Enhanced Performance
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