PUBLICACIÓN

NMR studies of sugar amides and thioamides

ACCEDER A LA PUBLICACIÓN: Scopus Orcid

Avalos, M., Babiano, R., Durán, C.J., Jiménez, J.L., Palacios, J.C.

1992 Journal of the Chemical Society, Perkin Transactions 2

CITAS

42

DOI

10.1039/p29920002205

EID

2-s2.0-37049089693

ISSN

1472-779X

BIBTEX

@article{babiano1992,title = {NMR studies of sugar amides and thioamides},journal = {Journal of the Chemical Society, Perkin Transactions 2},year = {1992},number = {12},pages = {2205-2215},author = {Avalos, M. and Babiano, R. and Dur{\'a}n, C.J. and Jim{\'e}nez, J.L. and Palacios, J.C.}}

AUTORES DE LA UEX

Carlos Javier Durán Valle

OTRAS PUBLICACIONES DE INTERÉS

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Optimizing P25-Rgo Composites For Pesticides Degradation: Elucidation Of Photo-Mechanism
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Synthesis, Characterization And Applications Of Carbon-Based Calcium Catalysts Deriving From Avocado Seeds For Biodiesel Production From Waste Cooking Oil
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Hydrothermal Carbonisation: An Eco-Friendly Method For The Production Of Carbon Adsorbents
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Activated Carbons As Catalyst In The Synthesis Of Fine Chemicals
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Prebiotic-Like Condensations Of Cyanamide And Glyoxal: Revisiting Intractable Biotars
Activated Carbons As Catalyst In The Synthesis Of Fine Chemicals
Prebiotic-Like Condensations Of Cyanamide And Glyoxal: Revisiting Intractable Biotars
On The Plausibility Of Pseudosugar Formation In Cometary Ices And Oxygen-Rich Tholins
Prebiotic-Like Condensations Of Cyanamide And Glyoxal: Revisiting Intractable Biotars
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
Computational Insights Into Cycloadditions Of Thioisomünchnones With Acetylenes: How Does Sulfur Escape From Cycloadducts?
A Further Look At Π-Delocalization And Hydrogen Bonding In 2-Arylmalondialdehydes
Computational Insights Into Cycloadditions Of Thioisomünchnones With Acetylenes: How Does Sulfur Escape From Cycloadducts?
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On The Optimization Of Activated Carbon-Supported Iron Catalysts In Catalytic Wet Peroxide Oxidation Process
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On The Optimization Of Activated Carbon-Supported Iron Catalysts In Catalytic Wet Peroxide Oxidation Process
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Rethinking Aromaticity In H-Bonded Systems. Caveats For Transition Structures Involving Hydrogen Transfer And Π-Delocalization
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Rethinking Aromaticity In H-Bonded Systems. Caveats For Transition Structures Involving Hydrogen Transfer And Π-Delocalization
Analysis Of Synergistic And Antagonistic Adsorption Of Heavy Metals And Acid Blue 25 On Activated Carbon From Ternary Systems
Rethinking Aromaticity In H-Bonded Systems. Caveats For Transition Structures Involving Hydrogen Transfer And Π-Delocalization
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Pseudo-Cyclic Structures Of Mono- And Di-Azaderivatives Of Malondialdehydes. Synthesis And Conformational Disentanglement By Computational Analyses
Analysis Of Synergistic And Antagonistic Adsorption Of Heavy Metals And Acid Blue 25 On Activated Carbon From Ternary Systems
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
Non-Covalent Derivatization Of Aminosilanized Titanium Alloy Implants Silver-Enhanced Coating Of Antibacterial Organics
Hydrazones From Hydroxy Naphthaldehydes. Part 2. Condensations With Aromatic N-Aminoheterocycles And Elucidation Of Tautomeric Structures
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
Acid-Activated Carbon Materials: Cheaper Alternative Catalysts For The Synthesis Of Substituted Quinolines
Photoinduced Electron Transfer Fluorometric Hg(Ii) Chemosensor Based On A Bodipy Armed With A Tetrapod Receptor
Acid-Activated Carbon Materials: Cheaper Alternative Catalysts For The Synthesis Of Substituted Quinolines
Controlled Silanization-Amination Reactions On The Ti6al4v Surface For Biomedical Applications
Acid-Activated Carbon Materials: Cheaper Alternative Catalysts For The Synthesis Of Substituted Quinolines
Controlled Silanization-Amination Reactions On The Ti6al4v Surface For Biomedical Applications
On The Prebiotic Synthesis Of D-Sugars Catalyzed By L-Peptides: Assessments From First-Principles Calculations
Controlled Silanization-Amination Reactions On The Ti6al4v Surface For Biomedical Applications
On The Prebiotic Synthesis Of D-Sugars Catalyzed By L-Peptides: Assessments From First-Principles Calculations
Fast And Reliable Location Of Stationary Points In A Reaction Path
On The Prebiotic Synthesis Of D-Sugars Catalyzed By L-Peptides: Assessments From First-Principles Calculations
Fast And Reliable Location Of Stationary Points In A Reaction Path
Mesoporous Carbon As An Efficient Catalyst For Alcoholysis And Aminolysis Of Epoxides
Fast And Reliable Location Of Stationary Points In A Reaction Path
Mesoporous Carbon As An Efficient Catalyst For Alcoholysis And Aminolysis Of Epoxides
Activated Carbon As A Catalyst For The Synthesis Of N-Alkylimidazoles And Imidazolium Ionic Liquids
Mesoporous Carbon As An Efficient Catalyst For Alcoholysis And Aminolysis Of Epoxides
Activated Carbon As A Catalyst For The Synthesis Of N-Alkylimidazoles And Imidazolium Ionic Liquids
Synergic Adsorption In The Simultaneous Removal Of Acid Blue 25 And Heavy Metals From Water Using A Ca(Po 3) 2-Modified Carbon
Activated Carbon As A Catalyst For The Synthesis Of N-Alkylimidazoles And Imidazolium Ionic Liquids
Synergic Adsorption In The Simultaneous Removal Of Acid Blue 25 And Heavy Metals From Water Using A Ca(Po 3) 2-Modified Carbon
Tautomerism In Schiff Bases. The Cases Of 2-Hydroxy-1-Naphthaldehyde And 1-Hydroxy-2-Naphthaldehyde Investigated In Solution And The Solid State
Synergic Adsorption In The Simultaneous Removal Of Acid Blue 25 And Heavy Metals From Water Using A Ca(Po 3) 2-Modified Carbon
Tautomerism In Schiff Bases. The Cases Of 2-Hydroxy-1-Naphthaldehyde And 1-Hydroxy-2-Naphthaldehyde Investigated In Solution And The Solid State
On The Enhanced Reactivity And Selectivity Of Triazole Formation In Molecular Flasks. A Theoretical Rationale
Tautomerism In Schiff Bases. The Cases Of 2-Hydroxy-1-Naphthaldehyde And 1-Hydroxy-2-Naphthaldehyde Investigated In Solution And The Solid State
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
Schiff Bases From Tris And Ortho-Hydroxyarenecarbaldehydes: Structures And Tautomeric Equilibria In The Solid State And In Solution
A Bioinspired Look At The Glucosinolate Metabolic Pathway. Structural Insights Into The Reaction Of Benzyl Isothiocyanate And D-Glucosamine
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
Push-Pull 1,3-Thiazolium-5-Thiolates. Formation Via Concerted And Stepwise Pathways, And Theoretical Evaluation Of Nlo Properties
Hydrazones From Hydroxy Naphthaldehydes And N-Aminoheterocycles: Structure And Stereodynamics
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
Unusual Aryl Migration In A Mesomeric Betaine In The Solid And Liquid State: Mechanistic Insights Into The Snar Reaction
An Anomeric Effect Drives The Regiospecific Ring-Opening Of 1,3-Oxazolidines Under Acetylating Conditions
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
A New Model For Mapping The Peptide Backbone: Predicting Proton Chemical Shifts In Proteins
Homochirality And Chemical Evolution: New Vistas And Reflections On Recent Models
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
Last Decade Of Research On Activated Carbons As Catalytic Support In Chemical Processes
Schiff Bases From D-Glucosamine And Aliphatic Ketones
Last Decade Of Research On Activated Carbons As Catalytic Support In Chemical Processes
The Effect Of Ultrasound On The N-Alkylation Of Imidazole Over Alkaline Carbons: Kinetic Aspects
Last Decade Of Research On Activated Carbons As Catalytic Support In Chemical Processes
The Effect Of Ultrasound On The N-Alkylation Of Imidazole Over Alkaline Carbons: Kinetic Aspects
Radioactive Content Of Charcoal
The Effect Of Ultrasound On The N-Alkylation Of Imidazole Over Alkaline Carbons: Kinetic Aspects
Radioactive Content Of Charcoal
Dissecting Competitive Mechanisms: Thionation Vs. Cycloaddition In The Reaction Of Thioisomünchnones With Isothiocyanates Under Microwave Irradiation
Radioactive Content Of Charcoal
Dissecting Competitive Mechanisms: Thionation Vs. Cycloaddition In The Reaction Of Thioisomünchnones With Isothiocyanates Under Microwave Irradiation
Thionation Of Mesoionics With Isothiocyanates: Evidence Supporting A Four-Step Domino Process And Ruling Out A [2 + 2] Mechanism
Dissecting Competitive Mechanisms: Thionation Vs. Cycloaddition In The Reaction Of Thioisomünchnones With Isothiocyanates Under Microwave Irradiation
Thionation Of Mesoionics With Isothiocyanates: Evidence Supporting A Four-Step Domino Process And Ruling Out A [2 + 2] Mechanism
Acidic Activated Carbons: An Efficient Catalyst For The Epoxide Ring-Opening Reaction With Ethanol
Thionation Of Mesoionics With Isothiocyanates: Evidence Supporting A Four-Step Domino Process And Ruling Out A [2 + 2] Mechanism
Acidic Activated Carbons: An Efficient Catalyst For The Epoxide Ring-Opening Reaction With Ethanol
An Efficient And Highly Diastereoselective Synthesis Of C-Glycosylated 1,3-Oxazolidines From N-Methyl-D-Glucamine
Acidic Activated Carbons: An Efficient Catalyst For The Epoxide Ring-Opening Reaction With Ethanol
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
Stepwise Cycloadditions Of Mesoionic Systems: Thionation Of Thioisomunchnones By Isothiocyanates
A Family Of Hydrogels Based On Ureido-Linked Aminopolyol-Derived Amphiphiles And Bolaamphiphiles: Synthesis, Gelation Under Thermal And Sonochemical Stimuli, And Mesomorphic Characterization
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
Control Microbiológico De Las Aguas De Consumo Humano En La Provincia De Badajoz En El Año 2006
Chiral N-Acyloxazolidines: Synthesis, Structure, And Mechanistic Insights
Control Microbiológico De Las Aguas De Consumo Humano En La Provincia De Badajoz En El Año 2006
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.
Control Microbiológico De Las Aguas De Consumo Humano En La Provincia De Badajoz En El Año 2006
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
Enhanced Diels-Alder Reactions: On The Role Of Mineral Catalysts And Microwave Irradiation In Ionic Liquids As Recyclable Media
Adaptación De La Asignatura Química Orgánica Al Proceso De Convergencia Europea En Los Estudios Degrado En Química De La Universidad De Extremadura
Enhanced Diels-Alder Reactions: On The Role Of Mineral Catalysts And Microwave Irradiation In Ionic Liquids As Recyclable Media
Adsorption Of Aqueous Mercury (Ii) Species By Commerical Activated Carbon Fibres With And Without Surface Modification
Enhanced Diels-Alder Reactions: On The Role Of Mineral Catalysts And Microwave Irradiation In Ionic Liquids As Recyclable Media
Adsorption Of Aqueous Mercury (Ii) Species By Commerical Activated Carbon Fibres With And Without Surface Modification
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
Adsorption Of Aqueous Mercury (Ii) Species By Commerical Activated Carbon Fibres With And Without Surface Modification
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
Preparation Of Charcoal From Cherry Stones
Synthesis Of Sugar Isocyanates And Their Application To The Formation Of Ureido-Linked Disaccharides
Preparation Of Charcoal From Cherry Stones
Geometrical Relationship Between Elemental Composition And Molecular Size In Carbonaceous Materials
Preparation Of Charcoal From Cherry Stones
Geometrical Relationship Between Elemental Composition And Molecular Size In Carbonaceous Materials
Ultrasound Accelerated Claisen-Schmidt Condensation: A Green Route To Chalcones
Geometrical Relationship Between Elemental Composition And Molecular Size In Carbonaceous Materials
Ultrasound Accelerated Claisen-Schmidt Condensation: A Green Route To Chalcones
Alkylation Of Imidazole Under Ultrasound Irradiation Over Alkaline Carbons
Ultrasound Accelerated Claisen-Schmidt Condensation: A Green Route To Chalcones
Alkylation Of Imidazole Under Ultrasound Irradiation Over Alkaline Carbons
Catalysis By Basic Carbons: Preparation Of Dihydropyridines
Alkylation Of Imidazole Under Ultrasound Irradiation Over Alkaline Carbons
Catalysis By Basic Carbons: Preparation Of Dihydropyridines
Green Chemistry: Efficient Epoxides Ring-Opening With 1-Butanol Under Microwave Irradiation
Catalysis By Basic Carbons: Preparation Of Dihydropyridines
Green Chemistry: Efficient Epoxides Ring-Opening With 1-Butanol Under Microwave Irradiation
Sonocatalysis In Solvent Free Conditions: An Efficient Eco-Friendly Methodology To Prepare Chalcones Using A New Type Of Amino Grafted Zeolites
Green Chemistry: Efficient Epoxides Ring-Opening With 1-Butanol Under Microwave Irradiation
Sonocatalysis In Solvent Free Conditions: An Efficient Eco-Friendly Methodology To Prepare Chalcones Using A New Type Of Amino Grafted Zeolites
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 4: Absolute Stereochemistry Of Carbohydrate-Based Imidazolidine-2-Ones And 2-Thiones With Axial And Central Chirality
Sonocatalysis In Solvent Free Conditions: An Efficient Eco-Friendly Methodology To Prepare Chalcones Using A New Type Of Amino Grafted Zeolites
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
Study Of Cherry Stones As Raw Material In Preparation Of Carbonaceous Adsorbents
Exploiting Synthetic Chemistry With Mesoionic Rings: Improvements Achieved With Thioisomünchnones
Study Of Cherry Stones As Raw Material In Preparation Of Carbonaceous Adsorbents
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Study Of Cherry Stones As Raw Material In Preparation Of Carbonaceous Adsorbents
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Sonocatalysis And Alkaline-Doped Carbons: An Efficient Method For The Synthesis Of Chalcones In Heterogeneous Media
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Sonocatalysis And Alkaline-Doped Carbons: An Efficient Method For The Synthesis Of Chalcones In Heterogeneous Media
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
Sonocatalysis And Alkaline-Doped Carbons: An Efficient Method For The Synthesis Of Chalcones In Heterogeneous Media
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
Symmetry Breaking: An Epistemological Note
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
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
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))
Symmetry Breaking By Spontaneous Crystallization - Is It The Most Plausible Source Of Terrestrial Handedness We Have Long Been Looking For? - A Reappraisal
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))
The Effect Of Ultrasound On The Catalytic Activity Of Alkaline Carbons: Preparation Of N-Alkyl Imidazoles
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))
The Effect Of Ultrasound On The Catalytic Activity Of Alkaline Carbons: Preparation Of N-Alkyl Imidazoles
Ultrasound-Promoted N-Propargylation Of Imidazole By Alkaline-Doped Carbons
The Effect Of Ultrasound On The Catalytic Activity Of Alkaline Carbons: Preparation Of N-Alkyl Imidazoles
Ultrasound-Promoted N-Propargylation Of Imidazole By Alkaline-Doped Carbons
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Ultrasound-Promoted N-Propargylation Of Imidazole By Alkaline-Doped Carbons
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
What Does Elementary Chirality Have To Do With Neutrinos?
Conformation Of Secondary Amides. A Predictive Algorithm That Correlates Dft-Calculated Structures And Experimental Proton Chemical Shifts
What Does Elementary Chirality Have To Do With Neutrinos?
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
What Does Elementary Chirality Have To Do With Neutrinos?
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
Generation And Fate Of A Novel Homochiral Mesoionic Dipole: Synthesis Of C-Nucleoside Analogs
Novel Acid-Catalyzed Rearrangement Of Tetrahydro-1,2,3,4-Tetrazines: Unexpected Formation Of Glycosazones
Generation And Fate Of A Novel Homochiral Mesoionic Dipole: Synthesis Of C-Nucleoside Analogs
Pore Structure Of Activated Carbons Prepared By Carbon Dioxide And Steam Activation At Different Temperatures From Extracted Rockrose
Generation And Fate Of A Novel Homochiral Mesoionic Dipole: Synthesis Of C-Nucleoside Analogs
Pore Structure Of Activated Carbons Prepared By Carbon Dioxide And Steam Activation At Different Temperatures From Extracted Rockrose
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
Pore Structure Of Activated Carbons Prepared By Carbon Dioxide And Steam Activation At Different Temperatures From Extracted Rockrose
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
Metalurgia General Práctica
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
Metalurgia General Práctica
Can We Predict The Conformational Preference Of Amides?
Metalurgia General Práctica
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
Conjugate Additions Of Heteronucleophiles To Enones And Alkynoates. A 'benign By Design' Functionalization Of Heteroaromatics
Three- And Four-Membered Rings From Cycloadditions Of 1,3-Thiazolium-4-Olates And Aldehydes
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
Pore Structure Of Chars And Activated Carbons Prepared Using Carbon Dioxide At Different Temperatures From Extracted Rockrose
Carbohydrate-Derived Dienes For Intramolecular And Asymmetric Diels-Alder Reactions
Pore Structure Of Chars And Activated Carbons Prepared Using Carbon Dioxide At Different Temperatures From Extracted Rockrose
Aplicabilidad De Un Carbón Vegetal En La Descontaminación Radiactiva De Aguas Naturales
Pore Structure Of Chars And Activated Carbons Prepared Using Carbon Dioxide At Different Temperatures From Extracted Rockrose
Aplicabilidad De Un Carbón Vegetal En La Descontaminación Radiactiva De Aguas Naturales
Estudio De La Microporosidad Estrecha De Carbones Activados Preparados Mediante Activación Con Aire A Partir De Huesos De Cereza
Aplicabilidad De Un Carbón Vegetal En La Descontaminación Radiactiva De Aguas Naturales
Estudio De La Microporosidad Estrecha De Carbones Activados Preparados Mediante Activación Con Aire A Partir De Huesos De Cereza
Estructura Química De Carbones Activados Preparados Mediante Activación Con Aire, Dióxido De Carbono Y Vapor De Agua A Partir De Jara
Estudio De La Microporosidad Estrecha De Carbones Activados Preparados Mediante Activación Con Aire A Partir De Huesos De Cereza
Estructura Química De Carbones Activados Preparados Mediante Activación Con Aire, Dióxido De Carbono Y Vapor De Agua A Partir De Jara
Estudio De Algunos Cambios En Un Carbón Vegetal Industrial Mediante Tratamientos Térmicos
Estructura Química De Carbones Activados Preparados Mediante Activación Con Aire, Dióxido De Carbono Y Vapor De Agua A Partir De Jara
Estudio De Algunos Cambios En Un Carbón Vegetal Industrial Mediante Tratamientos Térmicos
Carbonizados Y Carbones Activados Con Aire A 250º C Preparados A Partir De Un Carbón Industrial
Estudio De Algunos Cambios En Un Carbón Vegetal Industrial Mediante Tratamientos Térmicos
Carbonizados Y Carbones Activados Con Aire A 250º C Preparados A Partir De Un Carbón Industrial
Carbones Ácidos Y Química Fina: Relaciones De Esterificación
Carbonizados Y Carbones Activados Con Aire A 250º C Preparados A Partir De Un Carbón Industrial
Carbones Ácidos Y Química Fina: Relaciones De Esterificación
Reactions Of 2-Amino-2-Thiazolines With Isocyanates And Isothiocyanates. Chemical And Computational Studies On The Regioselectivity, Adduct Rearrangement, And Mechanistic Pathways
Carbones Ácidos Y Química Fina: Relaciones De Esterificación
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
Chemical Study Of Extracted Rockrose And Of Chars And Activated Carbons Prepared At Different Temperatures
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 2. Atropisomeric Behavior Of Monocyclic And Bicyclic Imidazolidine-2-Ones And 2- Thiones
Chemical Study Of Extracted Rockrose And Of Chars And Activated Carbons Prepared At Different Temperatures
Formation Of Oxygen Structures By Air Activation. A Study By Ft-Ir Spectroscopy
Chemical Study Of Extracted Rockrose And Of Chars And Activated Carbons Prepared At Different Temperatures
Formation Of Oxygen Structures By Air Activation. A Study By Ft-Ir Spectroscopy
Clay-Catalyzed Solventless Addition Reactions Of Furan With Α,β- Unsaturated Carbonyl Compounds
Formation Of Oxygen Structures By Air Activation. A Study By Ft-Ir Spectroscopy
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
Organic Chemical Structure And Structural Shrinkage Of Chars Prepared From Rockrose
Absolute Asymmetric Synthesis Under Physical Fields: Facts And Fictions
Organic Chemical Structure And Structural Shrinkage Of Chars Prepared From Rockrose
Asymmetric Tandem Reactions Based On Nitroalkenes: A One-Pot Construction Of Functionalized Chiral Bicycles By A Three-Component Reaction
Organic Chemical Structure And Structural Shrinkage Of Chars Prepared From Rockrose
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
Ft-Ir Study Of Rockrose And Of Char And Activated Carbon
A Simple, Cip-Based Notation System For The Unambiguous Specification Of Asymmetric Reactions
Ft-Ir Study Of Rockrose And Of Char And Activated Carbon
Heat Treatment Of Rockrose Char In Air. Effect On Surface Chemistry And Porous Texture
Ft-Ir Study Of Rockrose And Of Char And Activated Carbon
Heat Treatment Of Rockrose Char In Air. Effect On Surface Chemistry And Porous Texture
Münchnone-Alkene Cycloadditions: Deviations From The Fmo Theory. Theoretical Studies In The Search Of The Transition State
Heat Treatment Of Rockrose Char In Air. Effect On Surface Chemistry And Porous Texture
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
Condensation Of 2-Amino-2-Deoxysugars With Isothiocyanates. Synthesis Of Cis-1,2-Fused Glycopyrano Heterocycles.
A Novel Highly Diastereoselective Synthesis Of Chiral Dihydrothiophenes From Mesoionic Compounds
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
Structure Of Adducts Of 2-Arylaminothiazolines With Isocyanates And Isothiocyanates
Reaction Of Thioamides With Silver Carboxylates In Aprotic Media. A Nucleophilic Approach To The Synthesis Of Imides, Amides, And Nitriles
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
Nmr Studies Of Sugar Amides And Thioamides
Haloalkyl Isothiocyanates, Useful And Versatile Reagents In Heterocyclic Chemistry
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
Diastereofacial Selectivity In Diels-Alder Reactions Of Chiral 1,2-Diaza-1,3-Butadienes From Carbohydrates
A New Synthesis Of 6-Oxopyrimidinium-4-Olates. Theoretical Study Of The Regioselective Cycloaddition Of Arylisocyanates With A 1,3-Thiazolium-4-Olate System
Diastereofacial Selectivity In Diels-Alder Reactions Of Chiral 1,2-Diaza-1,3-Butadienes From Carbohydrates
Synthesis And Reactivity Toward Acetylenic Dipolarophiles Of Imidazo[2,1-B]thiazolium-3-Olate Systems
Diastereofacial Selectivity In Diels-Alder Reactions Of Chiral 1,2-Diaza-1,3-Butadienes From Carbohydrates
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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