PUBLICACIÓN

Elusive 2-aminofuran Diels-Alder substrates for a straightforward synthesis of polysubstituted anilines

ACCEDER A LA PUBLICACIÓN: Scopus Orcid

Neo A.G.; Bornadiego A.; Diaz J.; Marcaccini S.; Marcos C.F.

2013 Organic and Biomolecular Chemistry

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

JCR: 3.487

SJR: 1.492

CITAS

25

DOI

10.1039/c3ob41411f

EID

2-s2.0-84884199300

ISSN

1477-0520

BIBTEX

@article{RID:0428150508351-6816, title = {Elusive 2-aminofuran Diels-Alder substrates for a straightforward synthesis of polysubstituted anilines}, journal = {Organic & Biomolecular Chemistry}, year = {2013}, author = {Neo, Ana G. and Bornadiego, Ana and Diaz, Jesus and Marcaccini, Stefano and Marcos, Carlos F.}, volume = {11}, number = {38}, pages = {6546-6555} }

AUTORES DE LA UEX

Carlos María Fernández Marcos
Jesús Díaz Álvarez
Ana María Gómez Neo

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On The Reactivity Of 2-Alkyl-1,3-Thiazolium-4-Olates Toward Electrophiles
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Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
Base-Induced Photocyclization Of 1,2-Diaryl-1-Tosylethenes. A Mechanistically Novel Approach To Phenanthrenes And Phenanthrenoids
Reactivity Of 2-Methyl Thioisomünchnone With Acid Chlorides
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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