Portal Investigación UEx

Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides

Unlocking Enol-Ugi-Derived Conformationally Restricted Peptidomimetic Motifs

Elucidation Of The Pyridine Ring-Opening Mechanism Of 2,2′-Bipyridine Or 1,10-Phenanthroline Ligands At Re(I) Carbonyl Complexes

Unlocking Enol-Ugi-Derived Conformationally Restricted Peptidomimetic Motifs

Elucidation Of The Pyridine Ring-Opening Mechanism Of 2,2′-Bipyridine Or 1,10-Phenanthroline Ligands At Re(I) Carbonyl Complexes

Stefano Marcaccini: A Pioneer In Isocyanide Chemistry

Elucidation Of The Pyridine Ring-Opening Mechanism Of 2,2′-Bipyridine Or 1,10-Phenanthroline Ligands At Re(I) Carbonyl Complexes

Stefano Marcaccini: A Pioneer In Isocyanide Chemistry

The Castagnoli–cushman Reaction

Stefano Marcaccini: A Pioneer In Isocyanide Chemistry

The Castagnoli–cushman Reaction

Main Group Molecular Switches With Swivel Bifurcated To Trifurcated Hydrogen Bond Mode Of Action

The Castagnoli–cushman Reaction

Main Group Molecular Switches With Swivel Bifurcated To Trifurcated Hydrogen Bond Mode Of Action

1h Nmr To Analyse The Lipid Profile In The Glyceride Fraction Of Different Categories Of Iberian Dry-Cured Hams

Main Group Molecular Switches With Swivel Bifurcated To Trifurcated Hydrogen Bond Mode Of Action

1h Nmr To Analyse The Lipid Profile In The Glyceride Fraction Of Different Categories Of Iberian Dry-Cured Hams

Pre-Arranged Building Block Approach For The Orthogonal Synthesis Of An Unfolded Tetrameric Organic–inorganic Phosphazane Macrocycle

1h Nmr To Analyse The Lipid Profile In The Glyceride Fraction Of Different Categories Of Iberian Dry-Cured Hams

Pre-Arranged Building Block Approach For The Orthogonal Synthesis Of An Unfolded Tetrameric Organic–inorganic Phosphazane Macrocycle

Strongly Electron-Donating Triazolylidene Ligands: Cationic Metal Carbonyl Complexes Of 1-Methyl-1,2,3-Triazole As Triazolium Surrogates

Pre-Arranged Building Block Approach For The Orthogonal Synthesis Of An Unfolded Tetrameric Organic–inorganic Phosphazane Macrocycle

Strongly Electron-Donating Triazolylidene Ligands: Cationic Metal Carbonyl Complexes Of 1-Methyl-1,2,3-Triazole As Triazolium Surrogates

Size-Control In The Synthesis Of Oxo-Bridged Phosphazane Macrocycles Via A Modular Addition Approach

Strongly Electron-Donating Triazolylidene Ligands: Cationic Metal Carbonyl Complexes Of 1-Methyl-1,2,3-Triazole As Triazolium Surrogates

Size-Control In The Synthesis Of Oxo-Bridged Phosphazane Macrocycles Via A Modular Addition Approach

A Safe And Green Benzylic Radical Bromination Experiment

Size-Control In The Synthesis Of Oxo-Bridged Phosphazane Macrocycles Via A Modular Addition Approach

A Safe And Green Benzylic Radical Bromination Experiment

N-Bridged Acyclic Trimeric Poly-Cyclodiphosphazanes: Highly Tuneable Cyclodiphosphazane Building Blocks

A Safe And Green Benzylic Radical Bromination Experiment

N-Bridged Acyclic Trimeric Poly-Cyclodiphosphazanes: Highly Tuneable Cyclodiphosphazane Building Blocks

Influence Of The Nucleophilic Ligand On The Reactivity Of Carbonyl Rhenium(I) Complexes Towards Methyl Propiolate: A Computational Chemistry Perspective

N-Bridged Acyclic Trimeric Poly-Cyclodiphosphazanes: Highly Tuneable Cyclodiphosphazane Building Blocks

Influence Of The Nucleophilic Ligand On The Reactivity Of Carbonyl Rhenium(I) Complexes Towards Methyl Propiolate: A Computational Chemistry Perspective

Addition Of Re-Bonded Nucleophilic Ligands To Activated Alkynes: A Theoretical Rationalization

Influence Of The Nucleophilic Ligand On The Reactivity Of Carbonyl Rhenium(I) Complexes Towards Methyl Propiolate: A Computational Chemistry Perspective

Addition Of Re-Bonded Nucleophilic Ligands To Activated Alkynes: A Theoretical Rationalization

Multicomponet Synthesis Of Pyrrolo [3,4-A] Carbazole-1,3-Diones

Addition Of Re-Bonded Nucleophilic Ligands To Activated Alkynes: A Theoretical Rationalization

Multicomponet Synthesis Of Pyrrolo [3,4-A] Carbazole-1,3-Diones

Direct Multicomponent Synthesis Of Benzocoumarins

Multicomponet Synthesis Of Pyrrolo [3,4-A] Carbazole-1,3-Diones

Direct Multicomponent Synthesis Of Benzocoumarins

Tandem Synthesis Of Polycyclic Isoindoles

Direct Multicomponent Synthesis Of Benzocoumarins

Tandem Synthesis Of Polycyclic Isoindoles

Tandem Synthesis Of 4-Aminoxanthones Is Controlled By A Water-Assisted Tautomerization: A General Straightforward Reaction

Tandem Synthesis Of Polycyclic Isoindoles

Tandem Synthesis Of 4-Aminoxanthones Is Controlled By A Water-Assisted Tautomerization: A General Straightforward Reaction

Regiochemistry Control By Bipyridine Substituents In The Deprotonation Of Rei And Moii N-Alkylimidazole Complexes

Tandem Synthesis Of 4-Aminoxanthones Is Controlled By A Water-Assisted Tautomerization: A General Straightforward Reaction

Regiochemistry Control By Bipyridine Substituents In The Deprotonation Of Rei And Moii N-Alkylimidazole Complexes

Expeditious Multicomponent Synthesis Of Xanthone Dimers

Regiochemistry Control By Bipyridine Substituents In The Deprotonation Of Rei And Moii N-Alkylimidazole Complexes

Expeditious Multicomponent Synthesis Of Xanthone Dimers

Synthesis Of Unique Phosphazane Macrocycles Via Steric Activation Of C-N Bonds

Expeditious Multicomponent Synthesis Of Xanthone Dimers

Synthesis Of Unique Phosphazane Macrocycles Via Steric Activation Of C-N Bonds

Bifunctional Iminophosphorane Catalysed Enantioselective Sulfa-Michael Addition Of Alkyl Thiols To Alkenyl Benzimidazoles

Synthesis Of Unique Phosphazane Macrocycles Via Steric Activation Of C-N Bonds

Bifunctional Iminophosphorane Catalysed Enantioselective Sulfa-Michael Addition Of Alkyl Thiols To Alkenyl Benzimidazoles

Intermolecular C−c Coupling Between 1-Methyl-1,2,3-Triazole And 2,2′-Bipyridine Or 1,10-Phenanthroline In Moii Complexes

Bifunctional Iminophosphorane Catalysed Enantioselective Sulfa-Michael Addition Of Alkyl Thiols To Alkenyl Benzimidazoles

Intermolecular C−c Coupling Between 1-Methyl-1,2,3-Triazole And 2,2′-Bipyridine Or 1,10-Phenanthroline In Moii Complexes

Synthesis And The Optical And Electrochemical Properties Of Indium(Iii) Bis(Arylimino)acenaphthene Complexes

Intermolecular C−c Coupling Between 1-Methyl-1,2,3-Triazole And 2,2′-Bipyridine Or 1,10-Phenanthroline In Moii Complexes

Synthesis And The Optical And Electrochemical Properties Of Indium(Iii) Bis(Arylimino)acenaphthene Complexes

Insights On The Reactivity Of Terminal Phosphanido Metal Complexes Toward Activated Alkynes From Theoretical Computations

Synthesis And The Optical And Electrochemical Properties Of Indium(Iii) Bis(Arylimino)acenaphthene Complexes

Insights On The Reactivity Of Terminal Phosphanido Metal Complexes Toward Activated Alkynes From Theoretical Computations

Regioselective Synthesis Of Dihydroxanthones And Xanthones Through A Tandem Process

Insights On The Reactivity Of Terminal Phosphanido Metal Complexes Toward Activated Alkynes From Theoretical Computations

Regioselective Synthesis Of Dihydroxanthones And Xanthones Through A Tandem Process

Activation Of Aromatic C−c Bonds Of 2,2’-Bipyridine Ligands

Regioselective Synthesis Of Dihydroxanthones And Xanthones Through A Tandem Process

Activation Of Aromatic C−c Bonds Of 2,2’-Bipyridine Ligands

A Multi-Step Solvent-Free Mechanochemical Route To Indium(Iii) Complexes

Activation Of Aromatic C−c Bonds Of 2,2’-Bipyridine Ligands

A Multi-Step Solvent-Free Mechanochemical Route To Indium(Iii) Complexes

Regioselective Tandem [4 + 1]-[4 + 2] Synthesis Of Amino-Substituted Dihydroxanthones And Xanthones

A Multi-Step Solvent-Free Mechanochemical Route To Indium(Iii) Complexes

Regioselective Tandem [4 + 1]-[4 + 2] Synthesis Of Amino-Substituted Dihydroxanthones And Xanthones

Influence Of The N-N Coligand: C-C Coupling Instead Of Formation Of Imidazol-2-Yl Complexes At {Mo(Η3-Allyl)(Co)2} Fragments. Theoretical And Experimental Studies

Regioselective Tandem [4 + 1]-[4 + 2] Synthesis Of Amino-Substituted Dihydroxanthones And Xanthones

Influence Of The N-N Coligand: C-C Coupling Instead Of Formation Of Imidazol-2-Yl Complexes At {Mo(Η3-Allyl)(Co)2} Fragments. Theoretical And Experimental Studies

Steric C-N Bond Activation On The Dimeric Macrocycle [{P(Μ-Nr)}2(Μ-Nr)]2

Influence Of The N-N Coligand: C-C Coupling Instead Of Formation Of Imidazol-2-Yl Complexes At {Mo(Η3-Allyl)(Co)2} Fragments. Theoretical And Experimental Studies

Steric C-N Bond Activation On The Dimeric Macrocycle [{P(Μ-Nr)}2(Μ-Nr)]2

Synthesis Of 4-Aminoxanthones By An Uncatalyzed, Multicomponent Reaction

Steric C-N Bond Activation On The Dimeric Macrocycle [{P(Μ-Nr)}2(Μ-Nr)]2

Synthesis Of 4-Aminoxanthones By An Uncatalyzed, Multicomponent Reaction

Elusive 2-Aminofuran Diels-Alder Substrates For A Straightforward Synthesis Of Polysubstituted Anilines

Synthesis Of 4-Aminoxanthones By An Uncatalyzed, Multicomponent Reaction

Elusive 2-Aminofuran Diels-Alder Substrates For A Straightforward Synthesis Of Polysubstituted Anilines

Copper-Catalyzed Addition Of Nucleophilic Silicon To Aldehydes

Elusive 2-Aminofuran Diels-Alder Substrates For A Straightforward Synthesis Of Polysubstituted Anilines

Copper-Catalyzed Addition Of Nucleophilic Silicon To Aldehydes

Furo[3,4-B]chromones, And Not Pyrano[3,4-B]chromones, Are Obtained By The Reaction Of 3-Formylchromones With Isocyanides

Copper-Catalyzed Addition Of Nucleophilic Silicon To Aldehydes

Furo[3,4-B]chromones, And Not Pyrano[3,4-B]chromones, Are Obtained By The Reaction Of 3-Formylchromones With Isocyanides

Conjugate Addition Of Isocyanides To Chromone 3-Carboxylic Acid: An Efficient One-Pot Synthesis Of Chroman-4-One 2-Carboxamides

Furo[3,4-B]chromones, And Not Pyrano[3,4-B]chromones, Are Obtained By The Reaction Of 3-Formylchromones With Isocyanides

Conjugate Addition Of Isocyanides To Chromone 3-Carboxylic Acid: An Efficient One-Pot Synthesis Of Chroman-4-One 2-Carboxamides

Two Different Hydrogen Bond Donor Ligands Together: A Selectivity Improvement In Organometallic {Re(Co) 3} Anion Hosts

Conjugate Addition Of Isocyanides To Chromone 3-Carboxylic Acid: An Efficient One-Pot Synthesis Of Chroman-4-One 2-Carboxamides

Two Different Hydrogen Bond Donor Ligands Together: A Selectivity Improvement In Organometallic {Re(Co) 3} Anion Hosts

Imidazole To Nhc Rearrangements At Molybdenum Centers: An Experimental And Theoretical Study

Two Different Hydrogen Bond Donor Ligands Together: A Selectivity Improvement In Organometallic {Re(Co) 3} Anion Hosts

Imidazole To Nhc Rearrangements At Molybdenum Centers: An Experimental And Theoretical Study

Proline-Catalyzed Aldol Reactions Of Cyclic Diketones: Fluorine Modifies Pathways As Well As Transition States

Imidazole To Nhc Rearrangements At Molybdenum Centers: An Experimental And Theoretical Study

Proline-Catalyzed Aldol Reactions Of Cyclic Diketones: Fluorine Modifies Pathways As Well As Transition States

From Bis(N-Alkylimidazole) To Bis(Nh-Nhc) In Rhenium Carbonyl Complexes

Proline-Catalyzed Aldol Reactions Of Cyclic Diketones: Fluorine Modifies Pathways As Well As Transition States

From Bis(N-Alkylimidazole) To Bis(Nh-Nhc) In Rhenium Carbonyl Complexes

Effect Of The Nature Of The Substituent In N-Alkylimidazole Ligands On The Outcome Of Deprotonation: Ring Opening Versus The Formation Of N-Heterocyclic Carbene Complexes

From Bis(N-Alkylimidazole) To Bis(Nh-Nhc) In Rhenium Carbonyl Complexes

Effect Of The Nature Of The Substituent In N-Alkylimidazole Ligands On The Outcome Of Deprotonation: Ring Opening Versus The Formation Of N-Heterocyclic Carbene Complexes

Nanoscale Aggregation Phenomena At The Contact Line Of Air-Drying Pure Water Droplets On Silicon Revealed By Atomic Force Microscopy

Effect Of The Nature Of The Substituent In N-Alkylimidazole Ligands On The Outcome Of Deprotonation: Ring Opening Versus The Formation Of N-Heterocyclic Carbene Complexes

Nanoscale Aggregation Phenomena At The Contact Line Of Air-Drying Pure Water Droplets On Silicon Revealed By Atomic Force Microscopy

On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles

Nanoscale Aggregation Phenomena At The Contact Line Of Air-Drying Pure Water Droplets On Silicon Revealed By Atomic Force Microscopy

On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles

Ultrastructural And Physico-Chemical Heterogeneities Of Yeast Surfaces Revealed By Mapping Lateral-Friction And Normal-Adhesion Forces Using An Atomic Force Microscope

On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles

Ultrastructural And Physico-Chemical Heterogeneities Of Yeast Surfaces Revealed By Mapping Lateral-Friction And Normal-Adhesion Forces Using An Atomic Force Microscope

Computer-Assisted Design Of Asymmetric 1,3-Dipolar Cycloadditions Between Dimethylvinylborane And Chiral Nitrones

Ultrastructural And Physico-Chemical Heterogeneities Of Yeast Surfaces Revealed By Mapping Lateral-Friction And Normal-Adhesion Forces Using An Atomic Force Microscope

Computer-Assisted Design Of Asymmetric 1,3-Dipolar Cycloadditions Between Dimethylvinylborane And Chiral Nitrones

Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones

Computer-Assisted Design Of Asymmetric 1,3-Dipolar Cycloadditions Between Dimethylvinylborane And Chiral Nitrones

Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones

Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides

Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones

Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides

Unlocking Enol-Ugi-Derived Conformationally Restricted Peptidomimetic Motifs