PUBLICACIÓN

Unlocking Enol-Ugi-Derived Conformationally Restricted Peptidomimetic Motifs

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ACCEDER A LA PUBLICACIÓN: Scopus Orcid

Ramiro J.L.; Diaz J.; G. Neo A.; F. Marcos C.

2025 JOURNAL OF ORGANIC CHEMISTRY

CITAS

0

DOI

10.1021/acs.joc.5c00229

EID

2-s2.0-105001499784

ISSN

0022-3263

EISSN

1520-6904

AUTORES DE LA UEX

Carlos María Fernández Marcos
Jesús Díaz Álvarez

OTRAS PUBLICACIONES DE INTERÉS

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Non-Covalent Design Strategies For Topological Switching In Acyclic Bis-Cyclodiphosphazane Scaffolds
Classification Of Raw Cuts From Iberian And Celta Pigs Based On Lipid Analysis And Chemometrics
Elucidation Of The Pyridine Ring-Opening Mechanism Of 2,2′-Bipyridine Or 1,10-Phenanthroline Ligands At Re(I) Carbonyl Complexes
Classification Of Raw Cuts From Iberian And Celta Pigs Based On Lipid Analysis And Chemometrics
Elucidation Of The Pyridine Ring-Opening Mechanism Of 2,2′-Bipyridine Or 1,10-Phenanthroline Ligands At Re(I) Carbonyl Complexes
Machine Learning-Enabled Fatty Acid Quantification And Classification Of Pork From Autochthonous Breeds Using Low-Field 1h Nmr Spectroscopic Data
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Amide-Derived Enols In Enol–ugi Reactions: Expanding Horizons For Peptidomimetic Scaffold Synthesis
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Strongly Electron-Donating Triazolylidene Ligands: Cationic Metal Carbonyl Complexes Of 1-Methyl-1,2,3-Triazole As Triazolium Surrogates
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Regiochemistry Control By Bipyridine Substituents In The Deprotonation Of Rei And Moii N-Alkylimidazole Complexes
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Regiochemistry Control By Bipyridine Substituents In The Deprotonation Of Rei And Moii N-Alkylimidazole Complexes
Expeditious Multicomponent Synthesis Of Xanthone Dimers
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Selective Synthesis Of 3-Substituted Pyrrolidinones By Enol-Passerini And Anomalous Enol-Passerini Condensations
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Selective Synthesis Of 3-Substituted Pyrrolidinones By Enol-Passerini And Anomalous Enol-Passerini Condensations
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Selective Synthesis Of 3-Substituted Pyrrolidinones By Enol-Passerini And Anomalous Enol-Passerini Condensations
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An Easy Synthesis Of Diversely Functionalized 2h-Chromenes And Amido Amines By An Enol-Ugi Reaction
Intermolecular C−c Coupling Between 1-Methyl-1,2,3-Triazole And 2,2′-Bipyridine Or 1,10-Phenanthroline In Moii Complexes
An Easy Synthesis Of Diversely Functionalized 2h-Chromenes And Amido Amines By An Enol-Ugi Reaction
Intermolecular C−c Coupling Between 1-Methyl-1,2,3-Triazole And 2,2′-Bipyridine Or 1,10-Phenanthroline In Moii Complexes
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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
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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
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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
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A Multi-Step Solvent-Free Mechanochemical Route To Indium(Iii) Complexes
Enol-Ugi Reaction Of Hydroxycoumarins: Straightforward Synthesis Of Amino Acid Derived Coumarin Enamines
Regioselective Tandem [4 + 1]-[4 + 2] Synthesis Of Amino-Substituted Dihydroxanthones And Xanthones
Enol-Ugi Reaction Of Hydroxycoumarins: Straightforward Synthesis Of Amino Acid Derived Coumarin Enamines
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
Allylic Amination Of Passerini Adducts. Application To The Selective Synthesis Of Chromone-Substituted Α-And Γ-Amino Acid Peptidic And Retropeptidic Units
Synthesis Of 4-Aminoxanthones By An Uncatalyzed, Multicomponent Reaction
Allylic Amination Of Passerini Adducts. Application To The Selective Synthesis Of Chromone-Substituted Α-And Γ-Amino Acid Peptidic And Retropeptidic Units
Elusive 2-Aminofuran Diels-Alder Substrates For A Straightforward Synthesis Of Polysubstituted Anilines
Allylic Amination Of Passerini Adducts. Application To The Selective Synthesis Of Chromone-Substituted Α-And Γ-Amino Acid Peptidic And Retropeptidic Units
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
Enols As Feasible Acid Components In The Ugi Condensation
Copper-Catalyzed Addition Of Nucleophilic Silicon To Aldehydes
Enols As Feasible Acid Components In The Ugi Condensation
Furo[3,4-B]chromones, And Not Pyrano[3,4-B]chromones, Are Obtained By The Reaction Of 3-Formylchromones With Isocyanides
Enols As Feasible Acid Components In The Ugi Condensation
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
A Straightforward Synthesis Of 2-Aminobenzothiazoles From Herz Compounds
Conjugate Addition Of Isocyanides To Chromone 3-Carboxylic Acid: An Efficient One-Pot Synthesis Of Chroman-4-One 2-Carboxamides
A Straightforward Synthesis Of 2-Aminobenzothiazoles From Herz Compounds
A Multicomponent Approach To The Synthesis Of 1,3-Dicarbonylic Compounds
A Straightforward Synthesis Of 2-Aminobenzothiazoles From Herz Compounds
A Multicomponent Approach To The Synthesis Of 1,3-Dicarbonylic Compounds
Two Different Hydrogen Bond Donor Ligands Together: A Selectivity Improvement In Organometallic {Re(Co) 3} Anion Hosts
A Multicomponent Approach To The Synthesis Of 1,3-Dicarbonylic Compounds
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
Sequential Five-Component Synthesis Of Spiropyrrolidinochromanones
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
Sequential Five-Component Synthesis Of Spiropyrrolidinochromanones
Nanoscale Aggregation Phenomena At The Contact Line Of Air-Drying Pure Water Droplets On Silicon Revealed By Atomic Force Microscopy
Sequential Five-Component Synthesis Of Spiropyrrolidinochromanones
Nanoscale Aggregation Phenomena At The Contact Line Of Air-Drying Pure Water Droplets On Silicon Revealed By Atomic Force Microscopy
Studies On Isocyanides: Synthesis Of Tetrazolyl-Isoindolinones Via Tandem Ugi Four-Component Condensation/intramolecular Amidation
Nanoscale Aggregation Phenomena At The Contact Line Of Air-Drying Pure Water Droplets On Silicon Revealed By Atomic Force Microscopy
Studies On Isocyanides: Synthesis Of Tetrazolyl-Isoindolinones Via Tandem Ugi Four-Component Condensation/intramolecular Amidation
Multicomponent Synthesis Of Highly Substituted 2-Pyridones
Studies On Isocyanides: Synthesis Of Tetrazolyl-Isoindolinones Via Tandem Ugi Four-Component Condensation/intramolecular Amidation
Multicomponent Synthesis Of Highly Substituted 2-Pyridones
Photodynamic Cell-Kill Analysis Of Breast Tumor Cells With A Tamoxifen-Pyropheophorbide Conjugate
Multicomponent Synthesis Of Highly Substituted 2-Pyridones
Photodynamic Cell-Kill Analysis Of Breast Tumor Cells With A Tamoxifen-Pyropheophorbide Conjugate
Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives
Photodynamic Cell-Kill Analysis Of Breast Tumor Cells With A Tamoxifen-Pyropheophorbide Conjugate
Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives
On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives
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
Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives
Ultrastructural And Physico-Chemical Heterogeneities Of Yeast Surfaces Revealed By Mapping Lateral-Friction And Normal-Adhesion Forces Using An Atomic Force Microscope
Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives
Tert-Butyl Isocyanide
Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives
Tert-Butyl Isocyanide
Studies On Isocyanides. A Facile Synthesis Of 4,5-Dihydro-1,4- Benzothiazepin-3(2h)-Ones Via Post-Condensation Modifications Of The Ugi Reaction
Tert-Butyl Isocyanide
Studies On Isocyanides. A Facile Synthesis Of 4,5-Dihydro-1,4- Benzothiazepin-3(2h)-Ones Via Post-Condensation Modifications Of The Ugi Reaction
Indene And Pseudoazulene Discotic Liquid Crystals: A Synthetic And Structural Study
Studies On Isocyanides. A Facile Synthesis Of 4,5-Dihydro-1,4- Benzothiazepin-3(2h)-Ones Via Post-Condensation Modifications Of The Ugi Reaction
Indene And Pseudoazulene Discotic Liquid Crystals: A Synthetic And Structural Study
A New Synthesis Of Β-Keto Amides By Reduction Of Passerini Adducts
Indene And Pseudoazulene Discotic Liquid Crystals: A Synthetic And Structural Study
A New Synthesis Of Β-Keto Amides By Reduction Of Passerini Adducts
Computer-Assisted Design Of Asymmetric 1,3-Dipolar Cycloadditions Between Dimethylvinylborane And Chiral Nitrones
A New Synthesis Of Β-Keto Amides By Reduction Of Passerini Adducts
Computer-Assisted Design Of Asymmetric 1,3-Dipolar Cycloadditions Between Dimethylvinylborane And Chiral Nitrones
Synthesis Of Highly Branched Sulfur-Nitrogen Heterocycles By Cascade Cycloadditions Of [1,2]dithiolo[1,4]thiazines And [1,2]dithiolopyrroles
Computer-Assisted Design Of Asymmetric 1,3-Dipolar Cycloadditions Between Dimethylvinylborane And Chiral Nitrones
Synthesis Of Highly Branched Sulfur-Nitrogen Heterocycles By Cascade Cycloadditions Of [1,2]dithiolo[1,4]thiazines And [1,2]dithiolopyrroles
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
Synthesis Of Highly Branched Sulfur-Nitrogen Heterocycles By Cascade Cycloadditions Of [1,2]dithiolo[1,4]thiazines And [1,2]dithiolopyrroles
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
Affinity Labeling Of The Nuclear Vitamin D Receptor With Nonsteroidal Alkylating Agents
Non-Dipolar Behavior Of Mesoionic Heterocycles: Synthesis And Tautomerism Of 2-Alkylthioisomünchnones
Affinity Labeling Of The Nuclear Vitamin D Receptor With Nonsteroidal Alkylating Agents
Infrared Spectroscopy In The Study Of Renal Lithiasis
Affinity Labeling Of The Nuclear Vitamin D Receptor With Nonsteroidal Alkylating Agents
Infrared Spectroscopy In The Study Of Renal Lithiasis
Studies On Isocyanides And Related Compounds; A Facile Synthesis Of Functionalized 3(2h)-Pyridazinones Via Ugi Four-Component Condensation
Infrared Spectroscopy In The Study Of Renal Lithiasis
Studies On Isocyanides And Related Compounds; A Facile Synthesis Of Functionalized 3(2h)-Pyridazinones Via Ugi Four-Component Condensation
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Studies On Isocyanides And Related Compounds; A Facile Synthesis Of Functionalized 3(2h)-Pyridazinones Via Ugi Four-Component Condensation
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Synthesis Of Poly-Ferrocene Heterocycles By Cycloaddition Of Mono- Or Bis(Ferrocenecarbonyl)acetylenes And Bis[1,2]dithiolo[1,4]thiazinethiones
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Synthesis Of Poly-Ferrocene Heterocycles By Cycloaddition Of Mono- Or Bis(Ferrocenecarbonyl)acetylenes And Bis[1,2]dithiolo[1,4]thiazinethiones
Synthesis Of [1,3]dithiole And Spiro[1,3] Dithiole Thiopyran Derivatives Of The [1,2]dithiolo[1,4]thiazine Ring System
Synthesis Of Poly-Ferrocene Heterocycles By Cycloaddition Of Mono- Or Bis(Ferrocenecarbonyl)acetylenes And Bis[1,2]dithiolo[1,4]thiazinethiones
Synthesis Of [1,3]dithiole And Spiro[1,3] Dithiole Thiopyran Derivatives Of The [1,2]dithiolo[1,4]thiazine Ring System
New Chemistry Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles
Synthesis Of [1,3]dithiole And Spiro[1,3] Dithiole Thiopyran Derivatives Of The [1,2]dithiolo[1,4]thiazine Ring System
New Chemistry Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles
Derivatives Of Methyl 5-Methyl-4-Oxo-1,2,4,5,8,8a-Hexahydrocyclopropa[C]-Pyrrolo[3,2-E] Indole-7-Carboxylate: A Case Of Inverse Electronic Effects On The Reactivity Of Cc-1065 Derivatives
New Chemistry Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles
Derivatives Of Methyl 5-Methyl-4-Oxo-1,2,4,5,8,8a-Hexahydrocyclopropa[C]-Pyrrolo[3,2-E] Indole-7-Carboxylate: A Case Of Inverse Electronic Effects On The Reactivity Of Cc-1065 Derivatives
Synthesis Of Thiadiazole, Dithietane, And Imine Derivatives Of The [1,2]dithiolo[1,4]thiazine Ring System
Derivatives Of Methyl 5-Methyl-4-Oxo-1,2,4,5,8,8a-Hexahydrocyclopropa[C]-Pyrrolo[3,2-E] Indole-7-Carboxylate: A Case Of Inverse Electronic Effects On The Reactivity Of Cc-1065 Derivatives
Synthesis Of Thiadiazole, Dithietane, And Imine Derivatives Of The [1,2]dithiolo[1,4]thiazine Ring System
Glu-256 Is A Main Structural Determinant For Oligomerisation Of Human Arginase I
Synthesis Of Thiadiazole, Dithietane, And Imine Derivatives Of The [1,2]dithiolo[1,4]thiazine Ring System
Glu-256 Is A Main Structural Determinant For Oligomerisation Of Human Arginase I
Multicomponent Reactions: A Convenient Undergraduate Organic Chemistry Experiment
Glu-256 Is A Main Structural Determinant For Oligomerisation Of Human Arginase I
Multicomponent Reactions: A Convenient Undergraduate Organic Chemistry Experiment
Studies On Isocyanides And Related Compounds. Synthesis Of Furan Derivatives And Their Transformation Into Indole Derivatives
Multicomponent Reactions: A Convenient Undergraduate Organic Chemistry Experiment
Studies On Isocyanides And Related Compounds. Synthesis Of Furan Derivatives And Their Transformation Into Indole Derivatives
Synthesis Of Bis[1,2]dithiolo[1,4]thiazines And A [1,2]dithiolo[1,4]thiazine From Tertiary Diisopropylamines
Studies On Isocyanides And Related Compounds. Synthesis Of Furan Derivatives And Their Transformation Into Indole Derivatives
Synthesis Of Bis[1,2]dithiolo[1,4]thiazines And A [1,2]dithiolo[1,4]thiazine From Tertiary Diisopropylamines
Synthesis Of Sulfur-Rich 1,2-And 1,3-Dithiolo Disulfides And Thiodesaurines From Diisopropyl Sulfide
Synthesis Of Bis[1,2]dithiolo[1,4]thiazines And A [1,2]dithiolo[1,4]thiazine From Tertiary Diisopropylamines
Synthesis Of Sulfur-Rich 1,2-And 1,3-Dithiolo Disulfides And Thiodesaurines From Diisopropyl Sulfide
Bis[1,2]dithiolo[3,4-B][4',3'-E][1,4]thiazine-3,5-Dione, A Planar 1,4-Thiazine
Synthesis Of Sulfur-Rich 1,2-And 1,3-Dithiolo Disulfides And Thiodesaurines From Diisopropyl Sulfide
Bis[1,2]dithiolo[3,4-B][4',3'-E][1,4]thiazine-3,5-Dione, A Planar 1,4-Thiazine
Conversion Of W-Alkyldiisopropylàmines Into Yv,/v-Bis(5-Chloro-3-Oxo[1,2]dithiol-4-Yl)amines
Bis[1,2]dithiolo[3,4-B][4',3'-E][1,4]thiazine-3,5-Dione, A Planar 1,4-Thiazine
Conversion Of W-Alkyldiisopropylàmines Into Yv,/v-Bis(5-Chloro-3-Oxo[1,2]dithiol-4-Yl)amines
Selective Syntheses Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles From Hünig's Base
Conversion Of W-Alkyldiisopropylàmines Into Yv,/v-Bis(5-Chloro-3-Oxo[1,2]dithiol-4-Yl)amines
Selective Syntheses Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles From Hünig's Base
Tertiary Amine-S2cl2 Chemistry: Interception Of Reaction Intermediates
Selective Syntheses Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles From Hünig's Base
Tertiary Amine-S2cl2 Chemistry: Interception Of Reaction Intermediates
A Facile Synthesis Of Β-Lactams Based On The Isocyanide Chemistry
Tertiary Amine-S2cl2 Chemistry: Interception Of Reaction Intermediates
A Facile Synthesis Of Β-Lactams Based On The Isocyanide Chemistry
From Hünig's Base To Bis([1,2]dithiolo)- [1,4]thiazines In One Pot: The Fast Route To Highly Sulfurated Heterocycles
A Facile Synthesis Of Β-Lactams Based On The Isocyanide Chemistry
From Hünig's Base To Bis([1,2]dithiolo)- [1,4]thiazines In One Pot: The Fast Route To Highly Sulfurated Heterocycles
Studies On Isocyanides And Related Compounds. An Unusual Synthesis Of Functionalized Succinimides
From Hünig's Base To Bis([1,2]dithiolo)- [1,4]thiazines In One Pot: The Fast Route To Highly Sulfurated Heterocycles
Studies On Isocyanides And Related Compounds. An Unusual Synthesis Of Functionalized Succinimides
One-Pot Synthesis And Chemistry Of Bis[1,2]dithiolopyrroles
Studies On Isocyanides And Related Compounds. An Unusual Synthesis Of Functionalized Succinimides
One-Pot Synthesis And Chemistry Of Bis[1,2]dithiolopyrroles
Studies On Isocyanides And Related Compounds. A Novel Synthetic Route To 1,6-Dihydro-6-Oxopyridine-2-Carboxylic Acid Derivatives
One-Pot Synthesis And Chemistry Of Bis[1,2]dithiolopyrroles
Studies On Isocyanides And Related Compounds. A Novel Synthetic Route To 1,6-Dihydro-6-Oxopyridine-2-Carboxylic Acid Derivatives
Studies On The Synthesis Of The Antitumor Agent Cc-1065: Preparation Of Isopropyl 6-Hydroxy-7-Methoxy-4-(2-Nitrooxyethyl)indole-2-Carboxylate
Studies On Isocyanides And Related Compounds. A Novel Synthetic Route To 1,6-Dihydro-6-Oxopyridine-2-Carboxylic Acid Derivatives
Studies On The Synthesis Of The Antitumor Agent Cc-1065: Preparation Of Isopropyl 6-Hydroxy-7-Methoxy-4-(2-Nitrooxyethyl)indole-2-Carboxylate
Synthesis Of Enantiomerically Pure Tricarbonylchromium(0) Complexes Of Ortho Substituted Styrenes From S‐α‐methylbenzylamine
Studies On The Synthesis Of The Antitumor Agent Cc-1065: Preparation Of Isopropyl 6-Hydroxy-7-Methoxy-4-(2-Nitrooxyethyl)indole-2-Carboxylate
Synthesis Of Enantiomerically Pure Tricarbonylchromium(0) Complexes Of Ortho Substituted Styrenes From S‐α‐methylbenzylamine
Phenol Nitration From A 2-(Nitrooxy)ethyl Side Chain
Synthesis Of Enantiomerically Pure Tricarbonylchromium(0) Complexes Of Ortho Substituted Styrenes From S‐α‐methylbenzylamine
Phenol Nitration From A 2-(Nitrooxy)ethyl Side Chain
Organometallics In Synthesis. Part I: The Transition Elements
Phenol Nitration From A 2-(Nitrooxy)ethyl Side Chain
Organometallics In Synthesis. Part I: The Transition Elements
First Synthesis Of Sulfonyl Substituted Tricarbonyl(Η6- Arene)chromium(0) Complexed
Organometallics In Synthesis. Part I: The Transition Elements
First Synthesis Of Sulfonyl Substituted Tricarbonyl(Η6- Arene)chromium(0) Complexed
Sulfoxides And Stereochemical Control In Organometallic Chemistry
First Synthesis Of Sulfonyl Substituted Tricarbonyl(Η6- Arene)chromium(0) Complexed
Sulfoxides And Stereochemical Control In Organometallic Chemistry
Synthesis Of Tricarbonyliron(0) Complexes Of Itaconic Acid Derivatives
Sulfoxides And Stereochemical Control In Organometallic Chemistry
Synthesis Of Tricarbonyliron(0) Complexes Of Itaconic Acid Derivatives
New One-Pot Synthesis Of Alkyl Nitrates From Alcohols
Synthesis Of Tricarbonyliron(0) Complexes Of Itaconic Acid Derivatives
New One-Pot Synthesis Of Alkyl Nitrates From Alcohols
Synthesis Of Methyl 4-(2,2-Dimethoxyethyl)-6-Hydroxy-7-Methoxyindole-2-Carboxylate: A Potential Intermediate For The Synthesis Of The Central And Right Parts Of The Anticancer Antibiotic Cc-1065
New One-Pot Synthesis Of Alkyl Nitrates From Alcohols
Synthesis Of Methyl 4-(2,2-Dimethoxyethyl)-6-Hydroxy-7-Methoxyindole-2-Carboxylate: A Potential Intermediate For The Synthesis Of The Central And Right Parts Of The Anticancer Antibiotic Cc-1065
Unlocking Enol-Ugi-Derived Conformationally Restricted Peptidomimetic Motifs
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