PUBLICACIÓN

Studies on the synthesis of a hindered analogue of the antitumour agent CC-1065

ACCEDER A LA PUBLICACIÓN: Scopus

Neo A.G., Lopez C., Lopez A., Castedo L., Tojo G.

2013 TETRAHEDRON

Biochemistry (Q2), Drug Discovery (Q1), Organic Chemistry (Q1)

JCR: 2.817

SJR: 1.106

CITAS

5

DOI

10.1016/j.tet.2013.10.012

EID

2-s2.0-84888644766

ISSN

0040-4020

EISSN

1464-5416

AUTORES DE LA UEX

Ana María Gómez Neo

OTRAS PUBLICACIONES DE INTERÉS

Asymmetric Synthesis And Electrochemical Behaviour Of A C2 Chiral Bisferrocenyl Orthoquinone
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
Synthesis Of Imidazolocoumarins By The Amide-Directed Oxidative Cyclisation Of Enol-Ugi Derivatives
The Castagnoli–cushman Reaction
Synthesis Of Imidazolocoumarins By The Amide-Directed Oxidative Cyclisation Of Enol-Ugi Derivatives
Synthesis Of Chromeno[3,4-B]piperazines By An Enol-Ugi/reduction/cyclization Sequence
Synthesis Of Imidazolocoumarins By The Amide-Directed Oxidative Cyclisation Of Enol-Ugi Derivatives
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
Selective Synthesis Of 3-Substituted Pyrrolidinones By Enol-Passerini And Anomalous Enol-Passerini Condensations
Synthesis Of Heterocyclic Compounds By Photochemical Cyclizations
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
Allylic Amination Of Passerini Adducts. Application To The Selective Synthesis Of Chromone-Substituted Α-And Γ-Amino Acid Peptidic And Retropeptidic Units
Enol-Ugi Reaction Of Hydroxycoumarins: Straightforward Synthesis Of Amino Acid Derived Coumarin Enamines
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
Ugi Four-Component Condensation With Two Cleavable Components: The Easiest Synthesis Of 2,n-Diarylglycines
Photocyclization Of Tosylstilbenes As A Key Reaction In The Preparation Of An Analogue Of The Antitumor Agent Cc-1065
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
Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives
Multicomponent Synthesis Of Highly Substituted 2-Pyridones
Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives
Studies On Isocyanides. A Facile Synthesis Of 4,5-Dihydro-1,4- Benzothiazepin-3(2h)-Ones Via Post-Condensation Modifications Of The Ugi Reaction
Zinc Catalysed Ester Solvolysis. Application To The Synthesis Of Tartronic Acid Derivatives
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
Base-Induced Photocyclization Of 1,2-Diaryl-1-Tosylethenes. A Mechanistically Novel Approach To Phenanthrenes And Phenanthrenoids
Cyclopentathiadiazines, New Heterocyclic Materials From Cyclic Enaminonitriles
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
New Chemistry Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles
A New Addition-Rearrangement Of [1,4]thiazine-2-Thiones With Aryl-1,2,4-Triazoline-3,5-Diones
New Chemistry Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles
Asymmetric Synthesis And Electrochemical Behaviour Of A C2 Chiral Bisferrocenyl Orthoquinone
New Chemistry Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles
Asymmetric Synthesis And Electrochemical Behaviour Of A C2 Chiral Bisferrocenyl Orthoquinone
Classification Of Raw Cuts From Iberian And Celta Pigs Based On Lipid Analysis And Chemometrics
WEB ACCESIBLE