PUBLICACIÓN

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

ACCEDER A LA PUBLICACIÓN: Scopus Orcid

Shi X. et al.

2020 ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Catalysis (Q1), Chemistry (miscellaneous) (Q1)

JCR: 15.336

SJR: 5.831

CITAS

4

DOI

10.1002/anie.202008214

EID

2-s2.0-85091466892

ISSN

1433-7851

EISSN

1521-3773

BIBTEX

@article{Shi_2020, doi = {10.1002/anie.202008214}, url = {https://doi.org/10.1002%2Fanie.202008214}, year = 2020, month = {sep}, publisher = {Wiley}, author = {Xiaoyan Shi and Felix Le{\'{o}}n and Ying Sim and Shina Quek and Gavin Hum and Yi Xin Joycelyn Khoo and Zi Xuan Ng and Mian Yang Par and How Chee Ong and Varun K. Singh and Rakesh Ganguly and Jack K. Clegg and Jes{\'{u}}s D{\'{\i}}az and Felipe Garc{\'{\i}}a}, title = {N-Bridged Acyclic Trimeric Poly-Cyclodiphosphazanes: Highly Tuneable Cyclodiphosphazane Building Blocks}, journal = {Angewandte Chemie International Edition}}

AUTORES DE LA UEX

Jesús Díaz Álvarez

OTRAS PUBLICACIONES DE INTERÉS

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
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