Portal Investigación UEx

An Efficient And Highly Diastereoselective Synthesis Of C-Glycosylated 1,3-Oxazolidines From N-Methyl-D-Glucamine

Catalytic Screening For 1,2-Diol Protection: A Saccharose-Derived Hydrothermal Carbon Showcases Enhanced Performance

Novel Graphitic Oxynitrides As Photocatalysts For Sustainable H2 Production And Co2 Valorization. The Importance Of Self-Assembly For Catalytic Activity

Catalytic Screening For 1,2-Diol Protection: A Saccharose-Derived Hydrothermal Carbon Showcases Enhanced Performance

Novel Graphitic Oxynitrides As Photocatalysts For Sustainable H2 Production And Co2 Valorization. The Importance Of Self-Assembly For Catalytic Activity

Tuning Synthesis And Sonochemistry Forges Learning And Enhances Educational Training: Protection Of 1,3-Diols Under Heterogeneous Catalysis As Sustainable Case Study

Novel Graphitic Oxynitrides As Photocatalysts For Sustainable H2 Production And Co2 Valorization. The Importance Of Self-Assembly For Catalytic Activity

Tuning Synthesis And Sonochemistry Forges Learning And Enhances Educational Training: Protection Of 1,3-Diols Under Heterogeneous Catalysis As Sustainable Case Study

Understanding Bio-Orthogonal Strain-Driven Sydnone Cycloadditions: Data-Assisted Profiles And The Search For Linear Relationships

Tuning Synthesis And Sonochemistry Forges Learning And Enhances Educational Training: Protection Of 1,3-Diols Under Heterogeneous Catalysis As Sustainable Case Study

Understanding Bio-Orthogonal Strain-Driven Sydnone Cycloadditions: Data-Assisted Profiles And The Search For Linear Relationships

Use Of Artificial Intelligence By Science University Students

Understanding Bio-Orthogonal Strain-Driven Sydnone Cycloadditions: Data-Assisted Profiles And The Search For Linear Relationships

Use Of Artificial Intelligence By Science University Students

A True Reverse Anomeric Effect Does Exist After All: A Hydrogen Bonding Stereocontrolling Effect In 2-Iminoaldoses

Use Of Artificial Intelligence By Science University Students

A True Reverse Anomeric Effect Does Exist After All: A Hydrogen Bonding Stereocontrolling Effect In 2-Iminoaldoses

University Students’ Introduction To Science Communication

A True Reverse Anomeric Effect Does Exist After All: A Hydrogen Bonding Stereocontrolling Effect In 2-Iminoaldoses

University Students’ Introduction To Science Communication

¿sabe El Estudiantado Universitario Hablar En Público?

University Students’ Introduction To Science Communication

¿sabe El Estudiantado Universitario Hablar En Público?

Preparación De Carbamatos A Partir De Aminas Aromáticas Mediante Catálisis Heterogénea

¿sabe El Estudiantado Universitario Hablar En Público?

Preparación De Carbamatos A Partir De Aminas Aromáticas Mediante Catálisis Heterogénea

Síntesis De Acetales Derivados De 1,2-Dioles En Presencia De Catalizadores Ácidos Carbonosos

Preparación De Carbamatos A Partir De Aminas Aromáticas Mediante Catálisis Heterogénea

Síntesis De Acetales Derivados De 1,2-Dioles En Presencia De Catalizadores Ácidos Carbonosos

An Eco-Friendly And Switchable Carbon-Based Catalyst For Protection-Deprotection Of Vicinal Diols

Síntesis De Acetales Derivados De 1,2-Dioles En Presencia De Catalizadores Ácidos Carbonosos

An Eco-Friendly And Switchable Carbon-Based Catalyst For Protection-Deprotection Of Vicinal Diols

Developing Public Speaking Skills In European Education Area Students: Reflections From Seven Years Of Experience

An Eco-Friendly And Switchable Carbon-Based Catalyst For Protection-Deprotection Of Vicinal Diols

Developing Public Speaking Skills In European Education Area Students: Reflections From Seven Years Of Experience

Mechanistic Insights Into The Oxidative Degradation Of Formic And Oxalic Acids With Ozone And Oh Radical. A Computational Rationale

Developing Public Speaking Skills In European Education Area Students: Reflections From Seven Years Of Experience

Mechanistic Insights Into The Oxidative Degradation Of Formic And Oxalic Acids With Ozone And Oh Radical. A Computational Rationale

Novel Antagonist Of The Type 2 Lysophosphatidic Acid Receptor (Lpa2), Ucm-14216, Ameliorates Spinal Cord Injury In Mice

Mechanistic Insights Into The Oxidative Degradation Of Formic And Oxalic Acids With Ozone And Oh Radical. A Computational Rationale

Novel Antagonist Of The Type 2 Lysophosphatidic Acid Receptor (Lpa2), Ucm-14216, Ameliorates Spinal Cord Injury In Mice

On The Origin Of Sugar Handedness: Facts, Hypotheses And Missing Links-A Review

Novel Antagonist Of The Type 2 Lysophosphatidic Acid Receptor (Lpa2), Ucm-14216, Ameliorates Spinal Cord Injury In Mice

On The Origin Of Sugar Handedness: Facts, Hypotheses And Missing Links-A Review

Discovery And Mechanism Of Action Studies Of 4,6-Diphenylpyrimidine-2-Carbohydrazides As Utrophin Modulators For The Treatment Of Duchenne Muscular Dystrophy

On The Origin Of Sugar Handedness: Facts, Hypotheses And Missing Links-A Review

Discovery And Mechanism Of Action Studies Of 4,6-Diphenylpyrimidine-2-Carbohydrazides As Utrophin Modulators For The Treatment Of Duchenne Muscular Dystrophy

Targeting The Ftsz Allosteric Binding Site With A Novel Fluorescence Polarization Screen, Cytological And Structural Approaches For Antibacterial Discovery

Discovery And Mechanism Of Action Studies Of 4,6-Diphenylpyrimidine-2-Carbohydrazides As Utrophin Modulators For The Treatment Of Duchenne Muscular Dystrophy

Targeting The Ftsz Allosteric Binding Site With A Novel Fluorescence Polarization Screen, Cytological And Structural Approaches For Antibacterial Discovery

Organic Sonochemistry: A Chemist's Timely Perspective On Mechanisms And Reactivity

Targeting The Ftsz Allosteric Binding Site With A Novel Fluorescence Polarization Screen, Cytological And Structural Approaches For Antibacterial Discovery

Organic Sonochemistry: A Chemist's Timely Perspective On Mechanisms And Reactivity

A Novel Agonist Of The Type 1 Lysophosphatidic Acid Receptor (Lpa1), Ucm-05194, Shows Efficacy In Neuropathic Pain Amelioration

Organic Sonochemistry: A Chemist's Timely Perspective On Mechanisms And Reactivity

A Novel Agonist Of The Type 1 Lysophosphatidic Acid Receptor (Lpa1), Ucm-05194, Shows Efficacy In Neuropathic Pain Amelioration

Imine Or Enamine? Insights And Predictive Guidelines From The Electronic Effect Of Substituents In H-Bonded Salicylimines

A Novel Agonist Of The Type 1 Lysophosphatidic Acid Receptor (Lpa1), Ucm-05194, Shows Efficacy In Neuropathic Pain Amelioration

Imine Or Enamine? Insights And Predictive Guidelines From The Electronic Effect Of Substituents In H-Bonded Salicylimines

Mutarotation Of Aldoses: Getting A Deeper Knowledge Of A Classic Equilibrium Enabled By Computational Analyses

Imine Or Enamine? Insights And Predictive Guidelines From The Electronic Effect Of Substituents In H-Bonded Salicylimines

Mutarotation Of Aldoses: Getting A Deeper Knowledge Of A Classic Equilibrium Enabled By Computational Analyses

Isolation From Stevia Rebaudiana Of Dmdp Acetic Acid, A Novel Iminosugar Amino Acid: Synthesis And Glycosidase Inhibition Profile Of Glycine And Β-Alanine Pyrrolidine Amino Acids

Mutarotation Of Aldoses: Getting A Deeper Knowledge Of A Classic Equilibrium Enabled By Computational Analyses

Isolation From Stevia Rebaudiana Of Dmdp Acetic Acid, A Novel Iminosugar Amino Acid: Synthesis And Glycosidase Inhibition Profile Of Glycine And Β-Alanine Pyrrolidine Amino Acids

A Novel Agonist Of The Type 1 Lysophosphatidic Acid Receptor (Lpa1), Ucm-05194, Shows Efficacy In Neuropathic Pain Amelioration.

Isolation From Stevia Rebaudiana Of Dmdp Acetic Acid, A Novel Iminosugar Amino Acid: Synthesis And Glycosidase Inhibition Profile Of Glycine And Β-Alanine Pyrrolidine Amino Acids

A Novel Agonist Of The Type 1 Lysophosphatidic Acid Receptor (Lpa1), Ucm-05194, Shows Efficacy In Neuropathic Pain Amelioration.

The Dimroth Rearrangement As A Probable Cause For Structural Misassignments In Imidazo[1,2-A]pyrimidines: A 15n-Labelling Study And An Easy Method For The Determination Of Regiochemistry

A Novel Agonist Of The Type 1 Lysophosphatidic Acid Receptor (Lpa1), Ucm-05194, Shows Efficacy In Neuropathic Pain Amelioration.

The Dimroth Rearrangement As A Probable Cause For Structural Misassignments In Imidazo[1,2-A]pyrimidines: A 15n-Labelling Study And An Easy Method For The Determination Of Regiochemistry

Cycloadditions With Mesoionic Dipoles: Strategy And Control

The Dimroth Rearrangement As A Probable Cause For Structural Misassignments In Imidazo[1,2-A]pyrimidines: A 15n-Labelling Study And An Easy Method For The Determination Of Regiochemistry

Cycloadditions With Mesoionic Dipoles: Strategy And Control

The Structural Assembly Switch Of Cell Division Protein Ftsz Probed With Fluorescent Allosteric Inhibitors

Cycloadditions With Mesoionic Dipoles: Strategy And Control

The Structural Assembly Switch Of Cell Division Protein Ftsz Probed With Fluorescent Allosteric Inhibitors

Cycloadditions With Mesoionic Dipoles: Strategy And Control

The Structural Assembly Switch Of Cell Division Protein Ftsz Probed With Fluorescent Allosteric Inhibitors

Cycloadditions With Mesoionic Dipoles: Strategy And Control

Structural Essentials For Β-: N -Acetylhexosaminidase Inhibition By Amides Of Prolines, Pipecolic And Azetidine Carboxylic Acids

Cycloadditions With Mesoionic Dipoles: Strategy And Control

Structural Essentials For Β-: N -Acetylhexosaminidase Inhibition By Amides Of Prolines, Pipecolic And Azetidine Carboxylic Acids

Nine Of 16 Stereoisomeric Polyhydroxylated Proline Amides Are Potent Β-N-Acetylhexosaminidase Inhibitors

Structural Essentials For Β-: N -Acetylhexosaminidase Inhibition By Amides Of Prolines, Pipecolic And Azetidine Carboxylic Acids

Nine Of 16 Stereoisomeric Polyhydroxylated Proline Amides Are Potent Β-N-Acetylhexosaminidase Inhibitors

Carbohydrate Derived Bicyclic Azetidin-3-Ones As Scaffolds For Highly Functionalized Azetidines

Nine Of 16 Stereoisomeric Polyhydroxylated Proline Amides Are Potent Β-N-Acetylhexosaminidase Inhibitors

Carbohydrate Derived Bicyclic Azetidin-3-Ones As Scaffolds For Highly Functionalized Azetidines

Short And Sweet: D-Glucose To L-Glucose And L-Glucuronic Acid

Carbohydrate Derived Bicyclic Azetidin-3-Ones As Scaffolds For Highly Functionalized Azetidines

Short And Sweet: D-Glucose To L-Glucose And L-Glucuronic Acid

Synthesis Of The Enantiomers Of Xylnac And Lyxnac: Comparison Of Β-N-Acetylhexosaminidase Inhibition By The 8 Stereoisomers Of 2-N-Acetylamino-1,2,4-Trideoxy-1,4-Iminopentitols

Short And Sweet: D-Glucose To L-Glucose And L-Glucuronic Acid

Synthesis Of The Enantiomers Of Xylnac And Lyxnac: Comparison Of Β-N-Acetylhexosaminidase Inhibition By The 8 Stereoisomers Of 2-N-Acetylamino-1,2,4-Trideoxy-1,4-Iminopentitols

Kurz Und Knapp:l-Glucose Undl-Glucuronsäure Ausd-Glucose

Synthesis Of The Enantiomers Of Xylnac And Lyxnac: Comparison Of Β-N-Acetylhexosaminidase Inhibition By The 8 Stereoisomers Of 2-N-Acetylamino-1,2,4-Trideoxy-1,4-Iminopentitols

Kurz Und Knapp:l-Glucose Undl-Glucuronsäure Ausd-Glucose

Hydrazones From Hydroxy Naphthaldehydes. Part 2. Condensations With Aromatic N-Aminoheterocycles And Elucidation Of Tautomeric Structures

Kurz Und Knapp:l-Glucose Undl-Glucuronsäure Ausd-Glucose

Hydrazones From Hydroxy Naphthaldehydes. Part 2. Condensations With Aromatic N-Aminoheterocycles And Elucidation Of Tautomeric Structures

(3r,4s,5r,6r,7s)-3,4,5,7-Tetrahydroxyconidine, An Azetidine Analogue Of 6,7-Diepicastanospermine And A Conformationally Constrained D- Deoxyaltronojirimycin, From L-Arabinose

Hydrazones From Hydroxy Naphthaldehydes. Part 2. Condensations With Aromatic N-Aminoheterocycles And Elucidation Of Tautomeric Structures

(3r,4s,5r,6r,7s)-3,4,5,7-Tetrahydroxyconidine, An Azetidine Analogue Of 6,7-Diepicastanospermine And A Conformationally Constrained D- Deoxyaltronojirimycin, From L-Arabinose

C-Branched Iminosugars: Α-Glucosidase Inhibition By Enantiomers Of Isodmdp, Isodgdp, And Isodab- L -Isodmdp Compared To Miglitol And Miglustat

(3r,4s,5r,6r,7s)-3,4,5,7-Tetrahydroxyconidine, An Azetidine Analogue Of 6,7-Diepicastanospermine And A Conformationally Constrained D- Deoxyaltronojirimycin, From L-Arabinose

C-Branched Iminosugars: Α-Glucosidase Inhibition By Enantiomers Of Isodmdp, Isodgdp, And Isodab- L -Isodmdp Compared To Miglitol And Miglustat

Azetidine Iminosugars From The Cyclization Of 3,5-Di- O -Triflates Of Α-Furanosides And Of 2,4-Di- O -Triflates Of Β-Pyranosides Derived From Glucose

C-Branched Iminosugars: Α-Glucosidase Inhibition By Enantiomers Of Isodmdp, Isodgdp, And Isodab- L -Isodmdp Compared To Miglitol And Miglustat

Azetidine Iminosugars From The Cyclization Of 3,5-Di- O -Triflates Of Α-Furanosides And Of 2,4-Di- O -Triflates Of Β-Pyranosides Derived From Glucose

N-(2-Carboxyethyl)-2,5-Dideoxy-2,5-Imino-D-Mannonic Acid [(3r,4r,5r)-1-(2-Carboxyethyl)-3,4-Dihydroxy-5-Hydroxymethyl-L-Proline]

Azetidine Iminosugars From The Cyclization Of 3,5-Di- O -Triflates Of Α-Furanosides And Of 2,4-Di- O -Triflates Of Β-Pyranosides Derived From Glucose

N-(2-Carboxyethyl)-2,5-Dideoxy-2,5-Imino-D-Mannonic Acid [(3r,4r,5r)-1-(2-Carboxyethyl)-3,4-Dihydroxy-5-Hydroxymethyl-L-Proline]

Glycosidase Inhibition By All 10 Stereoisomeric 2,5-Dideoxy-2,5- Iminohexitols Prepared From The Enantiomers Of Glucuronolactone

N-(2-Carboxyethyl)-2,5-Dideoxy-2,5-Imino-D-Mannonic Acid [(3r,4r,5r)-1-(2-Carboxyethyl)-3,4-Dihydroxy-5-Hydroxymethyl-L-Proline]

Glycosidase Inhibition By All 10 Stereoisomeric 2,5-Dideoxy-2,5- Iminohexitols Prepared From The Enantiomers Of Glucuronolactone

Synthesis From D-Altrose Of (5 R,6 R,7 R,8 S)-5,7-Dihydroxy-8- Hydroxymethylconidine And 2,4-Dideoxy-2,4-Imino-D-Glucitol, Azetidine Analogues Of Swainsonine And 1,4-Dideoxy-1,4-Imino-D-Mannitol

Glycosidase Inhibition By All 10 Stereoisomeric 2,5-Dideoxy-2,5- Iminohexitols Prepared From The Enantiomers Of Glucuronolactone

Synthesis From D-Altrose Of (5 R,6 R,7 R,8 S)-5,7-Dihydroxy-8- Hydroxymethylconidine And 2,4-Dideoxy-2,4-Imino-D-Glucitol, Azetidine Analogues Of Swainsonine And 1,4-Dideoxy-1,4-Imino-D-Mannitol

Tautomerism In Schiff Bases. The Cases Of 2-Hydroxy-1-Naphthaldehyde And 1-Hydroxy-2-Naphthaldehyde Investigated In Solution And The Solid State

Synthesis From D-Altrose Of (5 R,6 R,7 R,8 S)-5,7-Dihydroxy-8- Hydroxymethylconidine And 2,4-Dideoxy-2,4-Imino-D-Glucitol, Azetidine Analogues Of Swainsonine And 1,4-Dideoxy-1,4-Imino-D-Mannitol

Tautomerism In Schiff Bases. The Cases Of 2-Hydroxy-1-Naphthaldehyde And 1-Hydroxy-2-Naphthaldehyde Investigated In Solution And The Solid State

Schiff Bases From Tris And Ortho-Hydroxyarenecarbaldehydes: Structures And Tautomeric Equilibria In The Solid State And In Solution

Tautomerism In Schiff Bases. The Cases Of 2-Hydroxy-1-Naphthaldehyde And 1-Hydroxy-2-Naphthaldehyde Investigated In Solution And The Solid State

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

Hydrazones From Hydroxy Naphthaldehydes And N-Aminoheterocycles: Structure And Stereodynamics

A Quantitative Structure-Reactivity Relationship In N-Acetyl Oxazolidines: An Electrostatic Interaction Controls Rotamer Population

Hydrazones From Hydroxy Naphthaldehydes And N-Aminoheterocycles: Structure And Stereodynamics

Schiff Bases From Tris And Formylpyridines: Structure And Mechanistic Rationale Aided By Dft Calculations

Hydrazones From Hydroxy Naphthaldehydes And N-Aminoheterocycles: Structure And Stereodynamics

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

An Efficient And Highly Diastereoselective Synthesis Of C-Glycosylated 1,3-Oxazolidines From N-Methyl-D-Glucamine

An Anomeric Effect Drives The Regiospecific Ring-Opening Of 1,3-Oxazolidines Under Acetylating Conditions

An Efficient And Highly Diastereoselective Synthesis Of C-Glycosylated 1,3-Oxazolidines From N-Methyl-D-Glucamine

Catalytic Screening For 1,2-Diol Protection: A Saccharose-Derived Hydrothermal Carbon Showcases Enhanced Performance