PUBLICACIÓN

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.

ACCEDER A LA PUBLICACIÓN: Dialnet

María Victoria Gil Álvarez;José Luis Jiménez Requejo, José Antonio Serrano Blázquez

2007 Experiencias de implantación de metodologías ECTS en cursos piloto completos: II Jornadas Nacionales de Metodologías ECTS. Badajoz, 19, 20 y 21 de septiembre de 2007

ISBN

9788477237907

AUTORES DE LA UEX

María Victoria Gil Álvarez

OTRAS PUBLICACIONES DE INTERÉS

Preparation Of C-Nucleosides By Dehydration Of Pentahydroxypentyl-Heterocycles: Steric Course And Mechanism
Targeting Cow's Milk Allergy Using Hypoallergenic Protein-Polyphenol Formulas: A Proof Of Concept
A Lutein And Zeaxanthin Enriched Extra Virgin Olive Oil As A Potential Nutraceutical Agent: A Pilot Study
Targeting Cow's Milk Allergy Using Hypoallergenic Protein-Polyphenol Formulas: A Proof Of Concept
A Lutein And Zeaxanthin Enriched Extra Virgin Olive Oil As A Potential Nutraceutical Agent: A Pilot Study
Natural Clays As Adsorbents For The Efficient Removal Of Antibiotic Ciprofloxacin From Wastewaters: Experimental And Theoretical Studies Using Dft Method
A Lutein And Zeaxanthin Enriched Extra Virgin Olive Oil As A Potential Nutraceutical Agent: A Pilot Study
Natural Clays As Adsorbents For The Efficient Removal Of Antibiotic Ciprofloxacin From Wastewaters: Experimental And Theoretical Studies Using Dft Method
Antioxidant Activity And Hypoallergenicity Of Egg Protein Matrices Containing Polyphenols From Citrus Waste
Natural Clays As Adsorbents For The Efficient Removal Of Antibiotic Ciprofloxacin From Wastewaters: Experimental And Theoretical Studies Using Dft Method
Antioxidant Activity And Hypoallergenicity Of Egg Protein Matrices Containing Polyphenols From Citrus Waste
Highlighting The Adsorption Mechanism Of A Fluoroquinolone Antibiotic From Wastewater On Carbon Xerogel By Experiments, Characterization, Modelling And Dft Simulation
Antioxidant Activity And Hypoallergenicity Of Egg Protein Matrices Containing Polyphenols From Citrus Waste
Highlighting The Adsorption Mechanism Of A Fluoroquinolone Antibiotic From Wastewater On Carbon Xerogel By Experiments, Characterization, Modelling And Dft Simulation
Influence Of Transition Metal-Based Activating Agent On The Properties And Catalytic Activity Of Sewage Sludge-Derived Catalysts. Insights On Mechanism, Dft Calculation And Degradation Pathways
Highlighting The Adsorption Mechanism Of A Fluoroquinolone Antibiotic From Wastewater On Carbon Xerogel By Experiments, Characterization, Modelling And Dft Simulation
Influence Of Transition Metal-Based Activating Agent On The Properties And Catalytic Activity Of Sewage Sludge-Derived Catalysts. Insights On Mechanism, Dft Calculation And Degradation Pathways
Food Allergens: When Friends Become Foes—caveats And Opportunities For Oral Immunotherapy Based On Deactivation Methods
Influence Of Transition Metal-Based Activating Agent On The Properties And Catalytic Activity Of Sewage Sludge-Derived Catalysts. Insights On Mechanism, Dft Calculation And Degradation Pathways
Food Allergens: When Friends Become Foes—caveats And Opportunities For Oral Immunotherapy Based On Deactivation Methods
Compuestos Fenólicos En Orujo Procedente De La Vinificación De La Uva Tinta: Efecto De Las Altas Presiones Hidrostáticas Y La Temperatura De Almacenamiento
Food Allergens: When Friends Become Foes—caveats And Opportunities For Oral Immunotherapy Based On Deactivation Methods
Compuestos Fenólicos En Orujo Procedente De La Vinificación De La Uva Tinta: Efecto De Las Altas Presiones Hidrostáticas Y La Temperatura De Almacenamiento
Efficient Removal Of Antibiotic Ciprofloxacin By Catalytic Wet Air Oxidation Using Sewage Sludge-Based Catalysts: Degradation Mechanism By Dft Studies
Compuestos Fenólicos En Orujo Procedente De La Vinificación De La Uva Tinta: Efecto De Las Altas Presiones Hidrostáticas Y La Temperatura De Almacenamiento
Efficient Removal Of Antibiotic Ciprofloxacin By Catalytic Wet Air Oxidation Using Sewage Sludge-Based Catalysts: Degradation Mechanism By Dft Studies
A Synthetically Benign One-Pot Construction Of Enamino-Xanthene Dyes
Efficient Removal Of Antibiotic Ciprofloxacin By Catalytic Wet Air Oxidation Using Sewage Sludge-Based Catalysts: Degradation Mechanism By Dft Studies
A Synthetically Benign One-Pot Construction Of Enamino-Xanthene Dyes
Insights Of Emerging Contaminants Removal In Real Water Matrices By Cwpo Using A Magnetic Catalyst
A Synthetically Benign One-Pot Construction Of Enamino-Xanthene Dyes
Insights Of Emerging Contaminants Removal In Real Water Matrices By Cwpo Using A Magnetic Catalyst
Control Of Listeria Monocytogenes In Sliced Dry-Cured Iberian Ham By High Pressure Processing In Combination With An Eco-Friendly Packaging Based On Chitosan, Nisin And Phytochemicals From Rice Bran
Insights Of Emerging Contaminants Removal In Real Water Matrices By Cwpo Using A Magnetic Catalyst
Control Of Listeria Monocytogenes In Sliced Dry-Cured Iberian Ham By High Pressure Processing In Combination With An Eco-Friendly Packaging Based On Chitosan, Nisin And Phytochemicals From Rice Bran
Magnetite-Based Catalyst In The Catalytic Wet Peroxide Oxidation For Different Aqueous Matrices Spiked With Naproxen–diclofenac Mixture
Control Of Listeria Monocytogenes In Sliced Dry-Cured Iberian Ham By High Pressure Processing In Combination With An Eco-Friendly Packaging Based On Chitosan, Nisin And Phytochemicals From Rice Bran
Magnetite-Based Catalyst In The Catalytic Wet Peroxide Oxidation For Different Aqueous Matrices Spiked With Naproxen–diclofenac Mixture
Cellulase-Assisted Extraction Of Phenolic Compounds From Rice Bran (Oryza Sativa L.): Process Optimization And Characterization
Magnetite-Based Catalyst In The Catalytic Wet Peroxide Oxidation For Different Aqueous Matrices Spiked With Naproxen–diclofenac Mixture
Cellulase-Assisted Extraction Of Phenolic Compounds From Rice Bran (Oryza Sativa L.): Process Optimization And Characterization
Deberían Invertirse Más Esfuerzos En Paliar La Situación Ante La Que Queda Una Científica Cuando Se Convierte En Madre
Cellulase-Assisted Extraction Of Phenolic Compounds From Rice Bran (Oryza Sativa L.): Process Optimization And Characterization
Deberían Invertirse Más Esfuerzos En Paliar La Situación Ante La Que Queda Una Científica Cuando Se Convierte En Madre
Antioxidant And Antimicrobial Evaluation Of Rice Bran (Oryza Sativa L.) Extracts In A Mayonnaise-Type Emulsion
Deberían Invertirse Más Esfuerzos En Paliar La Situación Ante La Que Queda Una Científica Cuando Se Convierte En Madre
Antioxidant And Antimicrobial Evaluation Of Rice Bran (Oryza Sativa L.) Extracts In A Mayonnaise-Type Emulsion
Effect Of Rice Bran Extract On The Preservation Of Pork Burger Treated With High Pressure Processing
Antioxidant And Antimicrobial Evaluation Of Rice Bran (Oryza Sativa L.) Extracts In A Mayonnaise-Type Emulsion
Effect Of Rice Bran Extract On The Preservation Of Pork Burger Treated With High Pressure Processing
Magnetic Fe3o4/multi-Walled Carbon Nanotubes Materials For A Highly Efficient Depletion Of Diclofenac By Catalytic Wet Peroxideoxidation
Effect Of Rice Bran Extract On The Preservation Of Pork Burger Treated With High Pressure Processing
Magnetic Fe3o4/multi-Walled Carbon Nanotubes Materials For A Highly Efficient Depletion Of Diclofenac By Catalytic Wet Peroxideoxidation
Synthesis And Antiproliferative Activity Of New 2-Glyco-3-Nitro-2h-Chromenes
Magnetic Fe3o4/multi-Walled Carbon Nanotubes Materials For A Highly Efficient Depletion Of Diclofenac By Catalytic Wet Peroxideoxidation
Synthesis And Antiproliferative Activity Of New 2-Glyco-3-Nitro-2h-Chromenes
Alergias Alimentarias:: Cuando La Adrenalina Salva Vidas, Pero La Formación, También.
Synthesis And Antiproliferative Activity Of New 2-Glyco-3-Nitro-2h-Chromenes
Alergias Alimentarias:: Cuando La Adrenalina Salva Vidas, Pero La Formación, También.
Nutracéutico De Aceite De Oliva Virgen Extra Enriquecido En Luteína Y Zeaxantina
Alergias Alimentarias:: Cuando La Adrenalina Salva Vidas, Pero La Formación, También.
Nutracéutico De Aceite De Oliva Virgen Extra Enriquecido En Luteína Y Zeaxantina
Bioavailability, Composition And Functional Characterization Of Extracts From Oryza Sativa L. Bran
Nutracéutico De Aceite De Oliva Virgen Extra Enriquecido En Luteína Y Zeaxantina
Bioavailability, Composition And Functional Characterization Of Extracts From Oryza Sativa L. Bran
Antiproliferative Activity Of New 2-Glyco-3-Nitro-1,2-Dihydroquinolines And Quinolines Synthesized Under Solventless Conditions Promoted By Neutral Alumina
Bioavailability, Composition And Functional Characterization Of Extracts From Oryza Sativa L. Bran
Antiproliferative Activity Of New 2-Glyco-3-Nitro-1,2-Dihydroquinolines And Quinolines Synthesized Under Solventless Conditions Promoted By Neutral Alumina
Computational Screening Of New Orthogonal Metal-Free Dipolar Cycloadditions Of Mesomeric Betaines
Antiproliferative Activity Of New 2-Glyco-3-Nitro-1,2-Dihydroquinolines And Quinolines Synthesized Under Solventless Conditions Promoted By Neutral Alumina
Computational Screening Of New Orthogonal Metal-Free Dipolar Cycloadditions Of Mesomeric Betaines
On The Dual Reactivity Of A Janus-Type Mesoionic Dipole: Experiments And Theoretical Validation
Computational Screening Of New Orthogonal Metal-Free Dipolar Cycloadditions Of Mesomeric Betaines
On The Dual Reactivity Of A Janus-Type Mesoionic Dipole: Experiments And Theoretical Validation
Mechanistic Studies Of 1,3-Dipolar Cycloadditions Of Bicyclic Thioisomünchnones With Alkenes. A Computational Rationale Focused On Donor-Acceptor Interactions
On The Dual Reactivity Of A Janus-Type Mesoionic Dipole: Experiments And Theoretical Validation
Mechanistic Studies Of 1,3-Dipolar Cycloadditions Of Bicyclic Thioisomünchnones With Alkenes. A Computational Rationale Focused On Donor-Acceptor Interactions
Can Lecturers Help Students Develop Public Speaking Skills? Reflexions From Experience
Mechanistic Studies Of 1,3-Dipolar Cycloadditions Of Bicyclic Thioisomünchnones With Alkenes. A Computational Rationale Focused On Donor-Acceptor Interactions
Can Lecturers Help Students Develop Public Speaking Skills? Reflexions From Experience
Ii Public Speaking Seminar: Analysis Of Results
Can Lecturers Help Students Develop Public Speaking Skills? Reflexions From Experience
Ii Public Speaking Seminar: Analysis Of Results
Química En Tu Plato
Ii Public Speaking Seminar: Analysis Of Results
Química En Tu Plato
Virgin Olive Oil Enriched With Lutein-Zeaxanthin From Spinacia Oleracea
Química En Tu Plato
Virgin Olive Oil Enriched With Lutein-Zeaxanthin From Spinacia Oleracea
Synthesis And Antiproliferative Activity Of Sulfa-Michael Adducts And Thiochromenes Derived From Carbohydrates
Virgin Olive Oil Enriched With Lutein-Zeaxanthin From Spinacia Oleracea
Synthesis And Antiproliferative Activity Of Sulfa-Michael Adducts And Thiochromenes Derived From Carbohydrates
Assessing Stereoelectronic Effects In Dipolar Cycloadditions Yielding Fused Thiazolopyridone Rings
Synthesis And Antiproliferative Activity Of Sulfa-Michael Adducts And Thiochromenes Derived From Carbohydrates
Assessing Stereoelectronic Effects In Dipolar Cycloadditions Yielding Fused Thiazolopyridone Rings
Synthesis And Antiproliferative Activity Of Peracetylated 2-Amino-1,2-Dideoxy-1-Nitro-D-Glycero-L-Manno And D-Glycero-D-Talo Heptitols
Assessing Stereoelectronic Effects In Dipolar Cycloadditions Yielding Fused Thiazolopyridone Rings
Synthesis And Antiproliferative Activity Of Peracetylated 2-Amino-1,2-Dideoxy-1-Nitro-D-Glycero-L-Manno And D-Glycero-D-Talo Heptitols
Green Chemical Synthesis And Click Reactions
Synthesis And Antiproliferative Activity Of Peracetylated 2-Amino-1,2-Dideoxy-1-Nitro-D-Glycero-L-Manno And D-Glycero-D-Talo Heptitols
Green Chemical Synthesis And Click Reactions
On Water Reactivity Between Carbohydrate-Derived Nitroalkenes And Furans
Green Chemical Synthesis And Click Reactions
On Water Reactivity Between Carbohydrate-Derived Nitroalkenes And Furans
Prebiotic-Like Condensations Of Cyanamide And Glyoxal: Revisiting Intractable Biotars
On Water Reactivity Between Carbohydrate-Derived Nitroalkenes And Furans
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?
Rethinking Aromaticity In H-Bonded Systems. Caveats For Transition Structures Involving Hydrogen Transfer And Π-Delocalization
Computational Insights Into Cycloadditions Of Thioisomünchnones With Acetylenes: How Does Sulfur Escape From Cycloadducts?
Rethinking Aromaticity In H-Bonded Systems. Caveats For Transition Structures Involving Hydrogen Transfer And Π-Delocalization
Phenolic Compounds And Antioxidant Capacity Of Virgin Olive Oil
Rethinking Aromaticity In H-Bonded Systems. Caveats For Transition Structures Involving Hydrogen Transfer And Π-Delocalization
Phenolic Compounds And Antioxidant Capacity Of Virgin Olive Oil
Expeditious 'on-Water' Cycloaddition Between N-Substituted Maleimides And Furans
Phenolic Compounds And Antioxidant Capacity Of Virgin Olive Oil
Expeditious 'on-Water' Cycloaddition Between N-Substituted Maleimides And Furans
Pseudo-Cyclic Structures Of Mono- And Di-Azaderivatives Of Malondialdehydes. Synthesis And Conformational Disentanglement By Computational Analyses
Expeditious 'on-Water' Cycloaddition Between N-Substituted Maleimides And Furans
Pseudo-Cyclic Structures Of Mono- And Di-Azaderivatives Of Malondialdehydes. Synthesis And Conformational Disentanglement By Computational Analyses
Stepwise Formation Of 1,3-Diazolium-4-Thiolates By Münchnone Cycloadditions: Promising Candidates For Nonlinear Optics
Pseudo-Cyclic Structures Of Mono- And Di-Azaderivatives Of Malondialdehydes. Synthesis And Conformational Disentanglement By Computational Analyses
Stepwise Formation Of 1,3-Diazolium-4-Thiolates By Münchnone Cycloadditions: Promising Candidates For Nonlinear Optics
Hydrazones From Hydroxy Naphthaldehydes. Part 2. Condensations With Aromatic N-Aminoheterocycles And Elucidation Of Tautomeric Structures
Stepwise Formation Of 1,3-Diazolium-4-Thiolates By Münchnone Cycloadditions: Promising Candidates For Nonlinear Optics
Hydrazones From Hydroxy Naphthaldehydes. Part 2. Condensations With Aromatic N-Aminoheterocycles And Elucidation Of Tautomeric Structures
Conjugated Nitrodienes. Synthesis And Reactivity
Hydrazones From Hydroxy Naphthaldehydes. Part 2. Condensations With Aromatic N-Aminoheterocycles And Elucidation Of Tautomeric Structures
Conjugated Nitrodienes. Synthesis And Reactivity
On The Prebiotic Synthesis Of D-Sugars Catalyzed By L-Peptides: Assessments From First-Principles Calculations
Conjugated Nitrodienes. Synthesis And Reactivity
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
Classical Insecticides:past, Present And Future
Fast And Reliable Location Of Stationary Points In A Reaction Path
Classical Insecticides:past, Present And Future
Tautomerism In Schiff Bases. The Cases Of 2-Hydroxy-1-Naphthaldehyde And 1-Hydroxy-2-Naphthaldehyde Investigated In Solution And The Solid State
Classical Insecticides:past, Present And Future
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
Discriminating Between Two Chiral Diastereoisomeric 7-Oxanitronorbornenes By Conventional X-Ray Powder Diffractometry
Hydrazones From Hydroxy Naphthaldehydes And N-Aminoheterocycles: Structure And Stereodynamics
Discriminating Between Two Chiral Diastereoisomeric 7-Oxanitronorbornenes By Conventional X-Ray Powder Diffractometry
Synthesis And Ring Opening Reactions Of 2-Glyco-1,4-Dimethyl-3-Nitro-7-Oxabicyclo[2.2.1]hept-5-Enes
Discriminating Between Two Chiral Diastereoisomeric 7-Oxanitronorbornenes By Conventional X-Ray Powder Diffractometry
Synthesis And Ring Opening Reactions Of 2-Glyco-1,4-Dimethyl-3-Nitro-7-Oxabicyclo[2.2.1]hept-5-Enes
Push-Pull 1,3-Thiazolium-5-Thiolates. Formation Via Concerted And Stepwise Pathways, And Theoretical Evaluation Of Nlo Properties
Synthesis And Ring Opening Reactions Of 2-Glyco-1,4-Dimethyl-3-Nitro-7-Oxabicyclo[2.2.1]hept-5-Enes
Push-Pull 1,3-Thiazolium-5-Thiolates. Formation Via Concerted And Stepwise Pathways, And Theoretical Evaluation Of Nlo Properties
Schiff Bases From Tris And Formylpyridines: Structure And Mechanistic Rationale Aided By Dft Calculations
Push-Pull 1,3-Thiazolium-5-Thiolates. Formation Via Concerted And Stepwise Pathways, And Theoretical Evaluation Of Nlo Properties
Schiff Bases From Tris And Formylpyridines: Structure And Mechanistic Rationale Aided By Dft Calculations
An Anomeric Effect Drives The Regiospecific Ring-Opening Of 1,3-Oxazolidines Under Acetylating Conditions
Schiff Bases From Tris And Formylpyridines: Structure And Mechanistic Rationale Aided By Dft Calculations
An Anomeric Effect Drives The Regiospecific Ring-Opening Of 1,3-Oxazolidines Under Acetylating Conditions
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
Laboratorio De Química: Generalidades Y Aspectos Básicos
Schiff Bases From D-Glucosamine And Aliphatic Ketones
Laboratorio De Química: Generalidades Y Aspectos Básicos
Synthesis Of Chiral 2-Furyl And 3-Nitro-7-Oxabicyclo[2.2.1]heptane Derivatives From Sugars
Laboratorio De Química: Generalidades Y Aspectos Básicos
Synthesis Of Chiral 2-Furyl And 3-Nitro-7-Oxabicyclo[2.2.1]heptane Derivatives From Sugars
Dissecting Competitive Mechanisms: Thionation Vs. Cycloaddition In The Reaction Of Thioisomünchnones With Isothiocyanates Under Microwave Irradiation
Synthesis Of Chiral 2-Furyl And 3-Nitro-7-Oxabicyclo[2.2.1]heptane Derivatives From Sugars
Dissecting Competitive Mechanisms: Thionation Vs. Cycloaddition In The Reaction Of Thioisomünchnones With Isothiocyanates Under Microwave Irradiation
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
New C-Aryl Alditols From Diels-Alder Adducts Of Sugar Nitroalkenes
Thionation Of Mesoionics With Isothiocyanates: Evidence Supporting A Four-Step Domino Process And Ruling Out A [2 + 2] Mechanism
New C-Aryl Alditols From Diels-Alder Adducts Of Sugar Nitroalkenes
Unexpected Reactions: From (2s,3r)-2-(Endo-D-Galacto-Pentaacetoxypentyl)-1, 4-Dimethyl-3-Exo-Nitro-7-Oxabicyclo[2.2.1]hept-5-Ene To Chiral Cyclic Ethers
New C-Aryl Alditols From Diels-Alder Adducts Of Sugar Nitroalkenes
Unexpected Reactions: From (2s,3r)-2-(Endo-D-Galacto-Pentaacetoxypentyl)-1, 4-Dimethyl-3-Exo-Nitro-7-Oxabicyclo[2.2.1]hept-5-Ene To Chiral Cyclic Ethers
An Efficient And Highly Diastereoselective Synthesis Of C-Glycosylated 1,3-Oxazolidines From N-Methyl-D-Glucamine
Unexpected Reactions: From (2s,3r)-2-(Endo-D-Galacto-Pentaacetoxypentyl)-1, 4-Dimethyl-3-Exo-Nitro-7-Oxabicyclo[2.2.1]hept-5-Ene To Chiral Cyclic Ethers
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
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.
Chiral N-Acyloxazolidines: Synthesis, Structure, And Mechanistic Insights
Adaptación Al Espacio Europeo De Educación Superior De La Asignatura Química Orgánica Básica En Los Estudios De Grado En Química En La Universidad De Extremadura.
Adaptación De La Asignatura Química Orgánica Al Proceso De Convergencia Europea En Los Estudios Degrado En Química De La Universidad De Extremadura
Adaptación Al Espacio Europeo De Educación Superior De La Asignatura Química Orgánica Básica En Los Estudios De Grado En Química En La Universidad De Extremadura.
Adaptación De La Asignatura Química Orgánica Al Proceso De Convergencia Europea En Los Estudios Degrado En Química De La Universidad De Extremadura
Experiencias De La Implantación De Un Plan De Acción Tutorial
Adaptación De La Asignatura Química Orgánica Al Proceso De Convergencia Europea En Los Estudios Degrado En Química De La Universidad De Extremadura
Experiencias De La Implantación De Un Plan De Acción Tutorial
Click Chemistry - What's In A Name? Triazole Synthesis And Beyond
Experiencias De La Implantación De Un Plan De Acción Tutorial
Click Chemistry - What's In A Name? Triazole Synthesis And Beyond
Aplicación Al Suelo De Compost De Estiércol Bovino Como Fertilizante Orgánico: Experiencias Prácticas En Cultivos De Frutales Y De Viñedo
Click Chemistry - What's In A Name? Triazole Synthesis And Beyond
Aplicación Al Suelo De Compost De Estiércol Bovino Como Fertilizante Orgánico: Experiencias Prácticas En Cultivos De Frutales Y De Viñedo
New Molecular Scaffolds: Synthesis Of (2r,3r)- And (2s,3s)-3-Nitro-7- Oxabicyclo[2.2.1]hept-5-Ene-2-Carbaldehyde From Furan
Aplicación Al Suelo De Compost De Estiércol Bovino Como Fertilizante Orgánico: Experiencias Prácticas En Cultivos De Frutales Y De Viñedo
New Molecular Scaffolds: Synthesis Of (2r,3r)- And (2s,3s)-3-Nitro-7- Oxabicyclo[2.2.1]hept-5-Ene-2-Carbaldehyde From Furan
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
New Molecular Scaffolds: Synthesis Of (2r,3r)- And (2s,3s)-3-Nitro-7- Oxabicyclo[2.2.1]hept-5-Ene-2-Carbaldehyde From Furan
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
Construction Of C-Nucleosides Diversified By [3+2] Cycloaddition From A Sugar-Based Mesoionic Ring
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
Construction Of C-Nucleosides Diversified By [3+2] Cycloaddition From A Sugar-Based Mesoionic Ring
Greener Media In Chemical Synthesis And Processing
Construction Of C-Nucleosides Diversified By [3+2] Cycloaddition From A Sugar-Based Mesoionic Ring
Greener Media In Chemical Synthesis And Processing
A One-Pot Domino Reaction In Constructing Isoorotate Bases And Their Nucleosides
Greener Media In Chemical Synthesis And Processing
A One-Pot Domino Reaction In Constructing Isoorotate Bases And Their Nucleosides
Synthesis Of Sugar Isocyanates And Their Application To The Formation Of Ureido-Linked Disaccharides
A One-Pot Domino Reaction In Constructing Isoorotate Bases And Their Nucleosides
Synthesis Of Sugar Isocyanates And Their Application To The Formation Of Ureido-Linked Disaccharides
Tandem Michael Addition And Intramolecular Aldol Cyclization Of 1,2-Dideoxy-1-Nitroheptitols Derived From Sugars
Synthesis Of Sugar Isocyanates And Their Application To The Formation Of Ureido-Linked Disaccharides
Tandem Michael Addition And Intramolecular Aldol Cyclization Of 1,2-Dideoxy-1-Nitroheptitols Derived From Sugars
New Trends In Pest Control: The Search For Greener Insecticides
Tandem Michael Addition And Intramolecular Aldol Cyclization Of 1,2-Dideoxy-1-Nitroheptitols Derived From Sugars
New Trends In Pest Control: The Search For Greener Insecticides
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 4: Absolute Stereochemistry Of Carbohydrate-Based Imidazolidine-2-Ones And 2-Thiones With Axial And Central Chirality
New Trends In Pest Control: The Search For Greener Insecticides
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 4: Absolute Stereochemistry Of Carbohydrate-Based Imidazolidine-2-Ones And 2-Thiones With Axial And Central Chirality
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 3: Rotational Isomerism Of Sterically Hindered Heteroaryl Imidazolidine-2-Ones And 2-Thiones
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 4: Absolute Stereochemistry Of Carbohydrate-Based Imidazolidine-2-Ones And 2-Thiones With Axial And Central Chirality
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 3: Rotational Isomerism Of Sterically Hindered Heteroaryl Imidazolidine-2-Ones And 2-Thiones
Exploiting Synthetic Chemistry With Mesoionic Rings: Improvements Achieved With Thioisomünchnones
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 3: Rotational Isomerism Of Sterically Hindered Heteroaryl Imidazolidine-2-Ones And 2-Thiones
Exploiting Synthetic Chemistry With Mesoionic Rings: Improvements Achieved With Thioisomünchnones
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Exploiting Synthetic Chemistry With Mesoionic Rings: Improvements Achieved With Thioisomünchnones
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Cetyltrimethylammonium Hydroxide (Ctaoh) As A General, Ecofriendly Catalyst For The Formation Of Carbon-Carbon Bond Through Nitroalkanes
An In-Depth Look At The Effect Of Lewis Acid Catalysts On Diels-Alder Cycloadditions In Ionic Liquids
Cetyltrimethylammonium Hydroxide (Ctaoh) As A General, Ecofriendly Catalyst For The Formation Of Carbon-Carbon Bond Through Nitroalkanes
A New, One Pot Synthesis Of Alkylated Methyl Tri- And Tetracarboxylate Derivatives By Nitrolkanes
Cetyltrimethylammonium Hydroxide (Ctaoh) As A General, Ecofriendly Catalyst For The Formation Of Carbon-Carbon Bond Through Nitroalkanes
A New, One Pot Synthesis Of Alkylated Methyl Tri- And Tetracarboxylate Derivatives By Nitrolkanes
Erratum: One-Pot Synthesis Of Polyfunctionalized Α, Β-Unsaturated Nitriles From Nitroalkanes (Tetrahedron Letters (2003) 44 (9033-9034))
A New, One Pot Synthesis Of Alkylated Methyl Tri- And Tetracarboxylate Derivatives By Nitrolkanes
Erratum: One-Pot Synthesis Of Polyfunctionalized Α, Β-Unsaturated Nitriles From Nitroalkanes (Tetrahedron Letters (2003) 44 (9033-9034))
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
Erratum: One-Pot Synthesis Of Polyfunctionalized Α, Β-Unsaturated Nitriles From Nitroalkanes (Tetrahedron Letters (2003) 44 (9033-9034))
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
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))
One-Pot Synthesis Of Polyfunctionalized Α,β-Unsaturated Nitriles From Nitroalkanes
Erratum: Thermal And Sonochemical Studies On The Diels-Alder Cycloadditions Of Masked O-Benzoquinones With Furans: New Insights Into The Reaction Mechanism (Journal Of Organic Chemistry (2003) 68 (7193-7203))
One-Pot Synthesis Of Polyfunctionalized Α,β-Unsaturated Nitriles From Nitroalkanes
Δ-Nitroalkanols As Precursors For The One-Pot Synthesis Of Substituted Tetrahydrofurans
One-Pot Synthesis Of Polyfunctionalized Α,β-Unsaturated Nitriles From Nitroalkanes
Δ-Nitroalkanols As Precursors For The One-Pot Synthesis Of Substituted Tetrahydrofurans
Michael Addition Of Α-Nitro Ketones To Conjugated Enones Under Solventless Conditions Using Silica
Δ-Nitroalkanols As Precursors For The One-Pot Synthesis Of Substituted Tetrahydrofurans
Michael Addition Of Α-Nitro Ketones To Conjugated Enones Under Solventless Conditions Using Silica
The First Synthesis Of Pentadecyl 6-Hydroxydodecanoate A Novel Compound Isolated From The Leaves Of Artabotrys Odoratissimus
Michael Addition Of Α-Nitro Ketones To Conjugated Enones Under Solventless Conditions Using Silica
The First Synthesis Of Pentadecyl 6-Hydroxydodecanoate A Novel Compound Isolated From The Leaves Of Artabotrys Odoratissimus
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
The First Synthesis Of Pentadecyl 6-Hydroxydodecanoate A Novel Compound Isolated From The Leaves Of Artabotrys Odoratissimus
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Thermal And Sonochemical Studies On The Diels-Alder Cycloadditions Of Masked O-Benzoquinones With Furans: New Insights Into The Reaction Mechanism
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Thermal And Sonochemical Studies On The Diels-Alder Cycloadditions Of Masked O-Benzoquinones With Furans: New Insights Into The Reaction Mechanism
1,3-Dipolar Cycloaddition Of 2-Dialkylaminothioisomünchnones With Aliphatic Aldehydes: Synthesis Of Β-Lactams And Thiiranes, Structure Elucidation, And Rationale For Chemoselective Fragmentation Of Cycloadducts
Thermal And Sonochemical Studies On The Diels-Alder Cycloadditions Of Masked O-Benzoquinones With Furans: New Insights Into The Reaction Mechanism
1,3-Dipolar Cycloaddition Of 2-Dialkylaminothioisomünchnones With Aliphatic Aldehydes: Synthesis Of Β-Lactams And Thiiranes, Structure Elucidation, And Rationale For Chemoselective Fragmentation Of Cycloadducts
Conformation Of Secondary Amides. A Predictive Algorithm That Correlates Dft-Calculated Structures And Experimental Proton Chemical Shifts
1,3-Dipolar Cycloaddition Of 2-Dialkylaminothioisomünchnones With Aliphatic Aldehydes: Synthesis Of Β-Lactams And Thiiranes, Structure Elucidation, And Rationale For Chemoselective Fragmentation Of Cycloadducts
Conformation Of Secondary Amides. A Predictive Algorithm That Correlates Dft-Calculated Structures And Experimental Proton Chemical Shifts
Preparation Of Enantiomerically Pure 4-Alkyl-5-Formyl-4-Nitrocyclohex-1-Enes From 5-Glyco-4-Nitrocyclohex-1-Enes
Conformation Of Secondary Amides. A Predictive Algorithm That Correlates Dft-Calculated Structures And Experimental Proton Chemical Shifts
Preparation Of Enantiomerically Pure 4-Alkyl-5-Formyl-4-Nitrocyclohex-1-Enes From 5-Glyco-4-Nitrocyclohex-1-Enes
Reactions Of Hydroxylated Sodium Nitronates With Acetic Anhydride/pyridine
Preparation Of Enantiomerically Pure 4-Alkyl-5-Formyl-4-Nitrocyclohex-1-Enes From 5-Glyco-4-Nitrocyclohex-1-Enes
Reactions Of Hydroxylated Sodium Nitronates With Acetic Anhydride/pyridine
Studies On The Chemistry Of Sodium Nitronates And Nitronic Esters Derived From 5-Glyco-4-Nitro-1-Cyclohexenes
Reactions Of Hydroxylated Sodium Nitronates With Acetic Anhydride/pyridine
Studies On The Chemistry Of Sodium Nitronates And Nitronic Esters Derived From 5-Glyco-4-Nitro-1-Cyclohexenes
Michael Addition Of Nitroalkanes To Dimethyl Citraconate, With Dbu As Base: An Unexpected, One-Pot Synthesis Of Polyfunctionalized Carbonyl Derivatives
Studies On The Chemistry Of Sodium Nitronates And Nitronic Esters Derived From 5-Glyco-4-Nitro-1-Cyclohexenes
Michael Addition Of Nitroalkanes To Dimethyl Citraconate, With Dbu As Base: An Unexpected, One-Pot Synthesis Of Polyfunctionalized Carbonyl Derivatives
What Does Elementary Chirality Have To Do With Neutrinos?
Michael Addition Of Nitroalkanes To Dimethyl Citraconate, With Dbu As Base: An Unexpected, One-Pot Synthesis Of Polyfunctionalized Carbonyl Derivatives
What Does Elementary Chirality Have To Do With Neutrinos?
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
Stereoselective Denitrohydrogenation Reactions Of 4-Alkyl-5-Glyco-4-Nitrocyclohex-1-Enes
Generation And Fate Of A Novel Homochiral Mesoionic Dipole: Synthesis Of C-Nucleoside Analogs
Stereoselective Denitrohydrogenation Reactions Of 4-Alkyl-5-Glyco-4-Nitrocyclohex-1-Enes
Nitrous Acid Elimination From 4-Alkyl-5-Formyl-4-Nitrocyclohex-1-Enes: Synthesis Of Mono And Bicyclic Benzene And Dihydrobenzene Derivatives
Stereoselective Denitrohydrogenation Reactions Of 4-Alkyl-5-Glyco-4-Nitrocyclohex-1-Enes
Nitrous Acid Elimination From 4-Alkyl-5-Formyl-4-Nitrocyclohex-1-Enes: Synthesis Of Mono And Bicyclic Benzene And Dihydrobenzene Derivatives
Synthesis Of Functionalized Nitrocyclohexene Derivatives From 2-Nitrocycloalkanones, Via Anionic Domino Reactions
Nitrous Acid Elimination From 4-Alkyl-5-Formyl-4-Nitrocyclohex-1-Enes: Synthesis Of Mono And Bicyclic Benzene And Dihydrobenzene Derivatives
Synthesis Of Functionalized Nitrocyclohexene Derivatives From 2-Nitrocycloalkanones, Via Anionic Domino Reactions
Stereoselective Synthesis Of (E)-4-Alkylidenecyclopent-2-En-1-Ones By A Tandem Ring Closure-Michael Addition-Elimination
Synthesis Of Functionalized Nitrocyclohexene Derivatives From 2-Nitrocycloalkanones, Via Anionic Domino Reactions
Stereoselective Synthesis Of (E)-4-Alkylidenecyclopent-2-En-1-Ones By A Tandem Ring Closure-Michael Addition-Elimination
Can We Predict The Conformational Preference Of Amides?
Stereoselective Synthesis Of (E)-4-Alkylidenecyclopent-2-En-1-Ones By A Tandem Ring Closure-Michael Addition-Elimination
Can We Predict The Conformational Preference Of Amides?
Carbohydrates As Chiral Controllers: Synthesis Of Dihydrothieno[2,3-C]furanones
Can We Predict The Conformational Preference Of Amides?
Carbohydrates As Chiral Controllers: Synthesis Of Dihydrothieno[2,3-C]furanones
A Cycloaddition Strategy For The Synthesis Of Thiirane-Containing Glycomimetics
Carbohydrates As Chiral Controllers: Synthesis Of Dihydrothieno[2,3-C]furanones
A Cycloaddition Strategy For The Synthesis Of Thiirane-Containing Glycomimetics
Synergic Effect Of Vicinal Stereocenters In [3 + 2] Cycloadditions Of Carbohydrate Azadipolarophiles And Mesoionic Dipoles: Origin Of Diastereofacial Selectivity
A Cycloaddition Strategy For The Synthesis Of Thiirane-Containing Glycomimetics
Synergic Effect Of Vicinal Stereocenters In [3 + 2] Cycloadditions Of Carbohydrate Azadipolarophiles And Mesoionic Dipoles: Origin Of Diastereofacial Selectivity
Three- And Four-Membered Rings From Cycloadditions Of 1,3-Thiazolium-4-Olates And Aldehydes
Synergic Effect Of Vicinal Stereocenters In [3 + 2] Cycloadditions Of Carbohydrate Azadipolarophiles And Mesoionic Dipoles: Origin Of Diastereofacial Selectivity
Three- And Four-Membered Rings From Cycloadditions Of 1,3-Thiazolium-4-Olates And Aldehydes
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
Carbohydrate-Derived Dienes For Intramolecular And Asymmetric Diels-Alder Reactions
Synthesis Of Dihydrothiophenes By An Amino-Directed Thioisomünchnone-Alkene Cycloaddition Reaction
Carbohydrate-Derived Dienes For Intramolecular And Asymmetric Diels-Alder Reactions
Procesos De Oxidación Avanzada: Aplicación A Compuestos Orgánicos En Disolución Acuosa
Carbohydrate-Derived Dienes For Intramolecular And Asymmetric Diels-Alder Reactions
Procesos De Oxidación Avanzada: Aplicación A Compuestos Orgánicos En Disolución Acuosa
Benzoxocin, Benzoxepin And Benzofuran Frameworks From 5-Glyco-4-Nitrocyclohex-1-Enes Through Nef Reaction And Intramolecular Cyclization
Procesos De Oxidación Avanzada: Aplicación A Compuestos Orgánicos En Disolución Acuosa
Benzoxocin, Benzoxepin And Benzofuran Frameworks From 5-Glyco-4-Nitrocyclohex-1-Enes Through Nef Reaction And Intramolecular Cyclization
Unexpected Transformations: From 5-Glyco-4-Nitrocyclohexenes To Bicyclic [3.3.1] Oximes Through Isoxazoline N-Oxides
Benzoxocin, Benzoxepin And Benzofuran Frameworks From 5-Glyco-4-Nitrocyclohex-1-Enes Through Nef Reaction And Intramolecular Cyclization
Unexpected Transformations: From 5-Glyco-4-Nitrocyclohexenes To Bicyclic [3.3.1] Oximes Through Isoxazoline N-Oxides
Reactions Of 2-Amino-2-Thiazolines With Isocyanates And Isothiocyanates. Chemical And Computational Studies On The Regioselectivity, Adduct Rearrangement, And Mechanistic Pathways
Unexpected Transformations: From 5-Glyco-4-Nitrocyclohexenes To Bicyclic [3.3.1] Oximes Through Isoxazoline N-Oxides
Reactions Of 2-Amino-2-Thiazolines With Isocyanates And Isothiocyanates. Chemical And Computational Studies On The Regioselectivity, Adduct Rearrangement, And Mechanistic Pathways
The First Density Functional Study On The [4 + 2]-Cycloaddition Reactions Of 1,2-Diaza-1,3-Butadiene With Alkenes
Reactions Of 2-Amino-2-Thiazolines With Isocyanates And Isothiocyanates. Chemical And Computational Studies On The Regioselectivity, Adduct Rearrangement, And Mechanistic Pathways
The First Density Functional Study On The [4 + 2]-Cycloaddition Reactions Of 1,2-Diaza-1,3-Butadiene With Alkenes
Computational Studies On The Bf3-Catalyzed Cycloaddition Of Furan With Methyl Vinyl Ketone: A New Look At Lewis Acid Catalysis
The First Density Functional Study On The [4 + 2]-Cycloaddition Reactions Of 1,2-Diaza-1,3-Butadiene With Alkenes
Computational Studies On The Bf3-Catalyzed Cycloaddition Of Furan With Methyl Vinyl Ketone: A New Look At Lewis Acid Catalysis
Diastereoselective Cycloadditions Of 1,3-Thiazolium-4-Olates With Chiral 1,2-Diaza-1,3-Butadienes
Computational Studies On The Bf3-Catalyzed Cycloaddition Of Furan With Methyl Vinyl Ketone: A New Look At Lewis Acid Catalysis
Diastereoselective Cycloadditions Of 1,3-Thiazolium-4-Olates With Chiral 1,2-Diaza-1,3-Butadienes
From Parity To Chirality: Chemical Implications Revisited
Diastereoselective Cycloadditions Of 1,3-Thiazolium-4-Olates With Chiral 1,2-Diaza-1,3-Butadienes
From Parity To Chirality: Chemical Implications Revisited
Chiral Autocatalysis: Where Stereochemistry Meets The Origin Of Life
From Parity To Chirality: Chemical Implications Revisited
Chiral Autocatalysis: Where Stereochemistry Meets The Origin Of Life
Sonochemical Cycloadditions Of O-Quinones. The Search For A Cation Radical Pathway
Chiral Autocatalysis: Where Stereochemistry Meets The Origin Of Life
Sonochemical Cycloadditions Of O-Quinones. The Search For A Cation Radical Pathway
Optically Active Sugar Thioamides From Δ-Gluconolactone
Sonochemical Cycloadditions Of O-Quinones. The Search For A Cation Radical Pathway
Optically Active Sugar Thioamides From Δ-Gluconolactone
[3+2]-Cycloadditions Of 2-Aminothioisomunchnones To Alkynes: Synthetic Scope And Mechanistic Insights
Optically Active Sugar Thioamides From Δ-Gluconolactone
[3+2]-Cycloadditions Of 2-Aminothioisomunchnones To Alkynes: Synthetic Scope And Mechanistic Insights
Understanding Diastereofacial Selection In Carbohydrate-Based Domino Cycloadditions: Semiempirical And Dft Calculations
[3+2]-Cycloadditions Of 2-Aminothioisomunchnones To Alkynes: Synthetic Scope And Mechanistic Insights
Understanding Diastereofacial Selection In Carbohydrate-Based Domino Cycloadditions: Semiempirical And Dft Calculations
Expeditious Formation Of 1,2,4-Triazine Derivatives Via A Thioisomunchnone Cycloaddition Reaction
Understanding Diastereofacial Selection In Carbohydrate-Based Domino Cycloadditions: Semiempirical And Dft Calculations
Expeditious Formation Of 1,2,4-Triazine Derivatives Via A Thioisomunchnone Cycloaddition Reaction
Atropisomeric Carbohydrate Imidazolidines: A Novel Class Of Nonbiaryl Atropisomers
Expeditious Formation Of 1,2,4-Triazine Derivatives Via A Thioisomunchnone Cycloaddition Reaction
Atropisomeric Carbohydrate Imidazolidines: A Novel Class Of Nonbiaryl Atropisomers
Unexpected Formation Of Β-Lactams And Penem Isosteres From Mesoionics: Sequential Ring-Opening-Rearrangement Of [3 + 2] Cycloadducts
Atropisomeric Carbohydrate Imidazolidines: A Novel Class Of Nonbiaryl Atropisomers
Unexpected Formation Of Β-Lactams And Penem Isosteres From Mesoionics: Sequential Ring-Opening-Rearrangement Of [3 + 2] Cycloadducts
Hetero-Diels-Alder Reactions Of Homochiral 1,2-Diaza-1,3-Butadienes With Diethyl Azodicarboxylate Under Microwave Irradiation. Theoretical Rationale Of The Stereochemical Outcome
Unexpected Formation Of Β-Lactams And Penem Isosteres From Mesoionics: Sequential Ring-Opening-Rearrangement Of [3 + 2] Cycloadducts
Hetero-Diels-Alder Reactions Of Homochiral 1,2-Diaza-1,3-Butadienes With Diethyl Azodicarboxylate Under Microwave Irradiation. Theoretical Rationale Of The Stereochemical Outcome
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 1. Stereoselective Synthesis Of 1-Aryl-5-Hydroxyimidazolidine-2-Thiones And Their Transformation Into Imidazoline-2-Thiones
Hetero-Diels-Alder Reactions Of Homochiral 1,2-Diaza-1,3-Butadienes With Diethyl Azodicarboxylate Under Microwave Irradiation. Theoretical Rationale Of The Stereochemical Outcome
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 1. Stereoselective Synthesis Of 1-Aryl-5-Hydroxyimidazolidine-2-Thiones And Their Transformation Into Imidazoline-2-Thiones
Diastereoselective Cycloadditions Of Nitroalkenes As An Approach To The Assembly Of Bicyclic Nitrogen Heterocycles
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 1. Stereoselective Synthesis Of 1-Aryl-5-Hydroxyimidazolidine-2-Thiones And Their Transformation Into Imidazoline-2-Thiones
Diastereoselective Cycloadditions Of Nitroalkenes As An Approach To The Assembly Of Bicyclic Nitrogen Heterocycles
Synthetic Variations Based On Low-Valent Chromium: New Developments
Diastereoselective Cycloadditions Of Nitroalkenes As An Approach To The Assembly Of Bicyclic Nitrogen Heterocycles
Synthetic Variations Based On Low-Valent Chromium: New Developments
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 2. Atropisomeric Behavior Of Monocyclic And Bicyclic Imidazolidine-2-Ones And 2- Thiones
Synthetic Variations Based On Low-Valent Chromium: New Developments
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 2. Atropisomeric Behavior Of Monocyclic And Bicyclic Imidazolidine-2-Ones And 2- Thiones
Clay-Catalyzed Solventless Addition Reactions Of Furan With Α,β- Unsaturated Carbonyl Compounds
Non-Biaryl Atropisomers Derived From Carbohydrates. Part 2. Atropisomeric Behavior Of Monocyclic And Bicyclic Imidazolidine-2-Ones And 2- Thiones
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
Importancia De Los Compuestos Fenólicos En Los Vinos
Asymmetric Tandem Reactions Based On Nitroalkenes: A One-Pot Construction Of Functionalized Chiral Bicycles By A Three-Component Reaction
Importancia De Los Compuestos Fenólicos En Los Vinos
Stereoselective Michael Addition Reactions Of 5-Glyco-4-Nitrocyclohex- 1-Enes
Importancia De Los Compuestos Fenólicos En Los Vinos
Stereoselective Michael Addition Reactions Of 5-Glyco-4-Nitrocyclohex- 1-Enes
Reactions Of Thioamides With Metal Carboxylates In Organic Media
Stereoselective Michael Addition Reactions Of 5-Glyco-4-Nitrocyclohex- 1-Enes
Reactions Of Thioamides With Metal Carboxylates In Organic Media
Nonlinear Stereochemical Effects In Asymmetric Reactions
Reactions Of Thioamides With Metal Carboxylates In Organic Media
Nonlinear Stereochemical Effects In Asymmetric Reactions
Nmr Studies And Semiempirical Calculations On The Structure Of Glycoamidines
Nonlinear Stereochemical Effects In Asymmetric Reactions
Nmr Studies And Semiempirical Calculations On The Structure Of Glycoamidines
Cycloaddition Chemistry Of 1,3-Thiazolium-4-Olate Systems. Reaction With Nitroalkenes And Interpretation Of Results Using Pm3 Calculations
Nmr Studies And Semiempirical Calculations On The Structure Of Glycoamidines
Cycloaddition Chemistry Of 1,3-Thiazolium-4-Olate Systems. Reaction With Nitroalkenes And Interpretation Of Results Using Pm3 Calculations
Substrate-Controlled Stereodifferentiation Of Tandem [4 + 2]/[3 + 2] Cycloadditions By A Vicinal Carbohydrate-Based Template
Cycloaddition Chemistry Of 1,3-Thiazolium-4-Olate Systems. Reaction With Nitroalkenes And Interpretation Of Results Using Pm3 Calculations
Substrate-Controlled Stereodifferentiation Of Tandem [4 + 2]/[3 + 2] Cycloadditions By A Vicinal Carbohydrate-Based Template
A Simple, Cip-Based Notation System For The Unambiguous Specification Of Asymmetric Reactions
Substrate-Controlled Stereodifferentiation Of Tandem [4 + 2]/[3 + 2] Cycloadditions By A Vicinal Carbohydrate-Based Template
A Simple, Cip-Based Notation System For The Unambiguous Specification Of Asymmetric Reactions
Münchnone-Alkene Cycloadditions: Deviations From The Fmo Theory. Theoretical Studies In The Search Of The Transition State
A Simple, Cip-Based Notation System For The Unambiguous Specification Of Asymmetric Reactions
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
Haloalkyl Isothiocyanates, Useful And Versatile Reagents In Heterocyclic Chemistry
Diastereoselective Synthesis Of Chiral Thiiranes By 1,3-Dipolar Cycloaddition Of Imidazo[2,1-B]thiazolium-4-Olate Systems With Aromatic Aldehydes
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
Synthesis Of Sugar N-(2-Thiazolin-2-Yl)thioureas
Synthesis And Reactivity Toward Acetylenic Dipolarophiles Of Imidazo[2,1-B]thiazolium-3-Olate Systems
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
Síntesis De Hidrobromuros De Glucopirano [2,1-D]-2-Tiazolinas
Reaction Of Glycosylisothiocyanates With 2-Chloroethylamine
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
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
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
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
New Acyclic-Sugar C-Nucleoside Analogs. Synthesis Of 2-(Alditol-1-Yl)-1-Alkyl-4,5,6,7-Tetrahydroindol-4-Ones
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
New Acyclic-Sugar C-Nucleoside Analogs. Synthesis Of 2-(Alditol-1-Yl)-1-Alkyl-4,5,6,7-Tetrahydroindol-4-Ones
Tioureas Derivadas De Carbohidratos. V. Isotiocianato Y Tioureas Derivadas De La 2-Amino-2-Desoxi-D-Glicero-Α-L-Gluco-Heptopiranosa
New Acyclic-Sugar C-Nucleoside Analogs. Synthesis Of 2-(Alditol-1-Yl)-1-Alkyl-4,5,6,7-Tetrahydroindol-4-Ones
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
Preparation Of C-Nucleosides By Dehydration Of Pentahydroxypentyl-Heterocycles: Steric Course And Mechanism
A Facile Synthesis Of C-Glycosylbarbiturates
Preparation Of C-Nucleosides By Dehydration Of Pentahydroxypentyl-Heterocycles: Steric Course And Mechanism
Targeting Cow's Milk Allergy Using Hypoallergenic Protein-Polyphenol Formulas: A Proof Of Concept
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