PUBLICACIÓN

Tandem synthesis of 4-aminoxanthones is controlled by a water-assisted tautomerization: a general straightforward reaction

ACCEDER A LA PUBLICACIÓN: Scopus Orcid

Bornadiego A., Diaz J., Marcos C.F.

2019 Organic and Biomolecular Chemistry

Biochemistry (Q2), Organic Chemistry (Q1), Physical and Theoretical Chemistry (Q1)

JCR: 3.412

SJR: 0.969

CITAS

17

DOI

10.1039/c8ob02527d

EID

2-s2.0-85061156833

ISSN

1477-0520

BIBTEX

@article{Bornadiego_2019, doi = {10.1039/c8ob02527d}, url = {https://doi.org/10.1039%2Fc8ob02527d}, year = 2019, publisher = {Royal Society of Chemistry ({RSC})}, author = {Ana Bornadiego and Jes{\'{u}}s D{\'{\i}}az and Carlos F. Marcos}, title = {Tandem synthesis of 4-aminoxanthones is controlled by a water-assisted tautomerization: a general straightforward reaction}, journal = {Organic {\&} Biomolecular Chemistry} }

AUTORES DE LA UEX

Carlos María Fernández Marcos
Jesús Díaz Álvarez

OTRAS PUBLICACIONES DE INTERÉS

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From Bis(N-Alkylimidazole) To Bis(Nh-Nhc) In Rhenium Carbonyl Complexes
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Sequential Five-Component Synthesis Of Spiropyrrolidinochromanones
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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
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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
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Affinity Labeling Of The Nuclear Vitamin D Receptor With Nonsteroidal Alkylating Agents
Infrared Spectroscopy In The Study Of Renal Lithiasis
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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
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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
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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
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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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