PUBLICACIÓN

Synthesis of chromeno[3,4-b]piperazines by an enol-ugi/reduction/cyclization sequence

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ACCEDER A LA PUBLICACIÓN: Scopus Orcid

Bornadiego A., Neo A.G., Marcos C.F.

2021 MOLECULES

Analytical Chemistry (Q2), Chemistry (miscellaneous) (Q2), Drug Discovery (Q2), Medicine (miscellaneous) (Q2), Molecular Medicine (Q3), Organic Chemistry (Q2), Pharmaceutical Science (Q1), Physical and Theoretical Chemistry (Q2)

JCR: 4.927

SJR: 0.705

CITAS

5

DOI

10.3390/molecules26051287

EID

2-s2.0-85102604957

EISSN

1420-3049

AUTORES DE LA UEX

Carlos María Fernández Marcos
Ana María Gómez Neo

OTRAS PUBLICACIONES DE INTERÉS

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
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Unlocking Enol-Ugi-Derived Conformationally Restricted Peptidomimetic Motifs
A Nuclear Magnetic Resonance Spectroscopy Metabolomic Approach To Renal Dysfunction In Canine Leishmaniasis
Classification Of Raw Cuts From Iberian And Celta Pigs Based On Lipid Analysis And Chemometrics
A Nuclear Magnetic Resonance Spectroscopy Metabolomic Approach To Renal Dysfunction In Canine Leishmaniasis
Classification Of Raw Cuts From Iberian And Celta Pigs Based On Lipid Analysis And Chemometrics
Machine Learning-Enabled Fatty Acid Quantification And Classification Of Pork From Autochthonous Breeds Using Low-Field 1h Nmr Spectroscopic Data
Classification Of Raw Cuts From Iberian And Celta Pigs Based On Lipid Analysis And Chemometrics
Machine Learning-Enabled Fatty Acid Quantification And Classification Of Pork From Autochthonous Breeds Using Low-Field 1h Nmr Spectroscopic Data
Synthesis Of Coumarin Dimers By A Microwave-Assisted Double Multicomponent Reaction
Machine Learning-Enabled Fatty Acid Quantification And Classification Of Pork From Autochthonous Breeds Using Low-Field 1h Nmr Spectroscopic Data
Synthesis Of Coumarin Dimers By A Microwave-Assisted Double Multicomponent Reaction
Amide-Derived Enols In Enol–ugi Reactions: Expanding Horizons For Peptidomimetic Scaffold Synthesis
Synthesis Of Coumarin Dimers By A Microwave-Assisted Double Multicomponent Reaction
Amide-Derived Enols In Enol–ugi Reactions: Expanding Horizons For Peptidomimetic Scaffold Synthesis
Stefano Marcaccini: A Pioneer In Isocyanide Chemistry
Amide-Derived Enols In Enol–ugi Reactions: Expanding Horizons For Peptidomimetic Scaffold Synthesis
Stefano Marcaccini: A Pioneer In Isocyanide Chemistry
The Castagnoli–cushman Reaction
Stefano Marcaccini: A Pioneer In Isocyanide Chemistry
The Castagnoli–cushman Reaction
Lipidomic Analysis And Classification Of Iberian Dry-Cured Hams With Low Field Nmr
The Castagnoli–cushman Reaction
Lipidomic Analysis And Classification Of Iberian Dry-Cured Hams With Low Field Nmr
1h Nmr To Analyse The Lipid Profile In The Glyceride Fraction Of Different Categories Of Iberian Dry-Cured Hams
Lipidomic Analysis And Classification Of Iberian Dry-Cured Hams With Low Field Nmr
1h Nmr To Analyse The Lipid Profile In The Glyceride Fraction Of Different Categories Of Iberian Dry-Cured Hams
Synthesis Of Imidazolocoumarins By The Amide-Directed Oxidative Cyclisation Of Enol-Ugi Derivatives
1h Nmr To Analyse The Lipid Profile In The Glyceride Fraction Of Different Categories Of Iberian Dry-Cured Hams
Synthesis Of Imidazolocoumarins By The Amide-Directed Oxidative Cyclisation Of Enol-Ugi Derivatives
Amide-Stabilized Enols In The Enol-Ugi Reaction: A Five-Component Synthesis Of Triamides
Synthesis Of Imidazolocoumarins By The Amide-Directed Oxidative Cyclisation Of Enol-Ugi Derivatives
Amide-Stabilized Enols In The Enol-Ugi Reaction: A Five-Component Synthesis Of Triamides
Multicomponent Reactions Of Isocyanides For The Preparation Of Low Molecular Weight Gelators: Preliminary Studies
Amide-Stabilized Enols In The Enol-Ugi Reaction: A Five-Component Synthesis Of Triamides
Multicomponent Reactions Of Isocyanides For The Preparation Of Low Molecular Weight Gelators: Preliminary Studies
Synthesis Of Chromeno[3,4-B]piperazines By An Enol-Ugi/reduction/cyclization Sequence
Multicomponent Reactions Of Isocyanides For The Preparation Of Low Molecular Weight Gelators: Preliminary Studies
Synthesis Of Chromeno[3,4-B]piperazines By An Enol-Ugi/reduction/cyclization Sequence
A Safe And Green Benzylic Radical Bromination Experiment
Synthesis Of Chromeno[3,4-B]piperazines By An Enol-Ugi/reduction/cyclization Sequence
A Safe And Green Benzylic Radical Bromination Experiment
Synthesis Of Heterocyclic Compounds By Photochemical Cyclizations
A Safe And Green Benzylic Radical Bromination Experiment
Synthesis Of Heterocyclic Compounds By Photochemical Cyclizations
Multicomponet Synthesis Of Pyrrolo [3,4-A] Carbazole-1,3-Diones
Synthesis Of Heterocyclic Compounds By Photochemical Cyclizations
Multicomponet Synthesis Of Pyrrolo [3,4-A] Carbazole-1,3-Diones
Tandem Synthesis Of Polycyclic Isoindoles
Multicomponet Synthesis Of Pyrrolo [3,4-A] Carbazole-1,3-Diones
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
Expeditious Multicomponent Synthesis Of Xanthone Dimers
Tandem Synthesis Of 4-Aminoxanthones Is Controlled By A Water-Assisted Tautomerization: A General Straightforward Reaction
Expeditious Multicomponent Synthesis Of Xanthone Dimers
Pyrrolidinodiones In Enol-Ugi, Enol-Passerini, And Anomalous Enol-Passerini Condensations
Expeditious Multicomponent Synthesis Of Xanthone Dimers
Pyrrolidinodiones In Enol-Ugi, Enol-Passerini, And Anomalous Enol-Passerini Condensations
Selective Synthesis Of 3-Substituted Pyrrolidinones By Enol-Passerini And Anomalous Enol-Passerini Condensations
Pyrrolidinodiones In Enol-Ugi, Enol-Passerini, And Anomalous Enol-Passerini Condensations
Selective Synthesis Of 3-Substituted Pyrrolidinones By Enol-Passerini And Anomalous Enol-Passerini Condensations
An Easy Synthesis Of Diversely Functionalized 2h-Chromenes And Amido Amines By An Enol-Ugi Reaction
Selective Synthesis Of 3-Substituted Pyrrolidinones By Enol-Passerini And Anomalous Enol-Passerini Condensations
An Easy Synthesis Of Diversely Functionalized 2h-Chromenes And Amido Amines By An Enol-Ugi Reaction
Enol-Ugi Reaction Of Hydroxycoumarins: Straightforward Synthesis Of Amino Acid Derived Coumarin Enamines
An Easy Synthesis Of Diversely Functionalized 2h-Chromenes And Amido Amines By An Enol-Ugi Reaction
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
Synthesis Of 4-Aminoxanthones By An Uncatalyzed, Multicomponent Reaction
Regioselective Tandem [4 + 1]-[4 + 2] Synthesis Of Amino-Substituted Dihydroxanthones And Xanthones
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
Studies On The Synthesis Of A Hindered Analogue Of The Antitumour Agent Cc-1065
Elusive 2-Aminofuran Diels-Alder Substrates For A Straightforward Synthesis Of Polysubstituted Anilines
Studies On The Synthesis Of A Hindered Analogue Of The Antitumour Agent Cc-1065
Enols As Feasible Acid Components In The Ugi Condensation
Studies On The Synthesis Of A Hindered Analogue Of The Antitumour Agent Cc-1065
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
Preparation Of Phenanthrenes By Photocyclization Of Stilbenes Containing A Tosyl Group On The Central Double Bond. A Versatile Approach To The Synthesis Of Phenanthrenes And Phenanthrenoids
A Multicomponent Approach To The Synthesis Of 1,3-Dicarbonylic Compounds
Preparation Of Phenanthrenes By Photocyclization Of Stilbenes Containing A Tosyl Group On The Central Double Bond. A Versatile Approach To The Synthesis Of Phenanthrenes And Phenanthrenoids
Simple 1-Dicyanomethylene-2-Chloro-3-Aminoindene Push-Pull Chromophores: Applications In Cation And Anion Sensing
Preparation Of Phenanthrenes By Photocyclization Of Stilbenes Containing A Tosyl Group On The Central Double Bond. A Versatile Approach To The Synthesis Of Phenanthrenes And Phenanthrenoids
Simple 1-Dicyanomethylene-2-Chloro-3-Aminoindene Push-Pull Chromophores: Applications In Cation And Anion Sensing
Sequential Five-Component Synthesis Of Spiropyrrolidinochromanones
Simple 1-Dicyanomethylene-2-Chloro-3-Aminoindene Push-Pull Chromophores: Applications In Cation And Anion Sensing
Sequential Five-Component Synthesis Of Spiropyrrolidinochromanones
Photocyclization Of Tosylstilbenes As A Key Reaction In The Preparation Of An Analogue Of The Antitumor Agent Cc-1065
Sequential Five-Component Synthesis Of Spiropyrrolidinochromanones
Photocyclization Of Tosylstilbenes As A Key Reaction In The Preparation Of An Analogue Of The Antitumor Agent Cc-1065
Studies On Isocyanides: Synthesis Of Tetrazolyl-Isoindolinones Via Tandem Ugi Four-Component Condensation/intramolecular Amidation
Photocyclization Of Tosylstilbenes As A Key Reaction In The Preparation Of An Analogue Of The Antitumor Agent Cc-1065
Studies On Isocyanides: Synthesis Of Tetrazolyl-Isoindolinones Via Tandem Ugi Four-Component Condensation/intramolecular Amidation
Ugi Four-Component Condensation With Two Cleavable Components: The Easiest Synthesis Of 2,n-Diarylglycines
Studies On Isocyanides: Synthesis Of Tetrazolyl-Isoindolinones Via Tandem Ugi Four-Component Condensation/intramolecular Amidation
Ugi Four-Component Condensation With Two Cleavable Components: The Easiest Synthesis Of 2,n-Diarylglycines
Multicomponent Synthesis Of Highly Substituted 2-Pyridones
Ugi Four-Component Condensation With Two Cleavable Components: The Easiest Synthesis Of 2,n-Diarylglycines
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
Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives
Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives
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
Cyclopentathiadiazines, Cyclohepta- And Cyclopentadithiazoles: New Materials And A Rich Heterocyclic Chemistry Of Cyclic Enaminonitriles
A New Synthesis Of Β-Keto Amides By Reduction Of Passerini Adducts
Cyclopentathiadiazines, Cyclohepta- And Cyclopentadithiazoles: New Materials And A Rich Heterocyclic Chemistry Of Cyclic Enaminonitriles
Cyclopentathiadiazines, New Heterocyclic Materials From Cyclic Enaminonitriles
Cyclopentathiadiazines, Cyclohepta- And Cyclopentadithiazoles: New Materials And A Rich Heterocyclic Chemistry Of Cyclic Enaminonitriles
Cyclopentathiadiazines, New Heterocyclic Materials From Cyclic Enaminonitriles
Synthesis Of Highly Branched Sulfur-Nitrogen Heterocycles By Cascade Cycloadditions Of [1,2]dithiolo[1,4]thiazines And [1,2]dithiolopyrroles
Cyclopentathiadiazines, New Heterocyclic Materials From Cyclic Enaminonitriles
Synthesis Of Highly Branched Sulfur-Nitrogen Heterocycles By Cascade Cycloadditions Of [1,2]dithiolo[1,4]thiazines And [1,2]dithiolopyrroles
Affinity Labeling Of The Nuclear Vitamin D Receptor With Nonsteroidal Alkylating Agents
Synthesis Of Highly Branched Sulfur-Nitrogen Heterocycles By Cascade Cycloadditions Of [1,2]dithiolo[1,4]thiazines And [1,2]dithiolopyrroles
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
Base-Induced Photocyclization Of 1,2-Diaryl-1-Tosylethenes. A Mechanistically Novel Approach To Phenanthrenes And Phenanthrenoids
Studies On Isocyanides And Related Compounds; A Facile Synthesis Of Functionalized 3(2h)-Pyridazinones Via Ugi Four-Component Condensation
Base-Induced Photocyclization Of 1,2-Diaryl-1-Tosylethenes. A Mechanistically Novel Approach To Phenanthrenes And Phenanthrenoids
A New Addition-Rearrangement Of [1,4]thiazine-2-Thiones With Aryl-1,2,4-Triazoline-3,5-Diones
Base-Induced Photocyclization Of 1,2-Diaryl-1-Tosylethenes. A Mechanistically Novel Approach To Phenanthrenes And Phenanthrenoids
A New Addition-Rearrangement Of [1,4]thiazine-2-Thiones With Aryl-1,2,4-Triazoline-3,5-Diones
Synthesis Of Poly-Ferrocene Heterocycles By Cycloaddition Of Mono- Or Bis(Ferrocenecarbonyl)acetylenes And Bis[1,2]dithiolo[1,4]thiazinethiones
A New Addition-Rearrangement Of [1,4]thiazine-2-Thiones With Aryl-1,2,4-Triazoline-3,5-Diones
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
Asymmetric Synthesis And Electrochemical Behaviour Of A C2 Chiral Bisferrocenyl Orthoquinone
Conversion Of W-Alkyldiisopropylàmines Into Yv,/v-Bis(5-Chloro-3-Oxo[1,2]dithiol-4-Yl)amines
Asymmetric Synthesis And Electrochemical Behaviour Of A C2 Chiral Bisferrocenyl Orthoquinone
Selective Syntheses Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles From Hünig's Base
Asymmetric Synthesis And Electrochemical Behaviour Of A C2 Chiral Bisferrocenyl Orthoquinone
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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