PUBLICACIÓN

An easy synthesis of diversely functionalized 2H-chromenes and amido amines by an enol-Ugi reaction

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ACCEDER A LA PUBLICACIÓN: Scopus Orcid

Neo A.G., Castellano T.G., Marcos C.F.

2017 ARKIVOC

Organic Chemistry (Q4)

JCR: 1.048

SJR: 0.262

CITAS

6

DOI

10.3998/ark.5550190.p009.775

EID

2-s2.0-85014559808

ISSN

1551-7004

EISSN

1551-7012

BIBTEX

@article{RID:1221170650128-6998, title = {An easy synthesis of diversely functionalized 2H-chromenes and amido amines by an enol-Ugi reaction}, journal = {Arkivoc}, year = {2017}, author = {Neo, A. G. and Castellano, T. G. and Marcos, C. F.}, pages = {21-31} }

AUTORES DE LA UEX

Carlos María Fernández Marcos
Ana María Gómez Neo

OTRAS PUBLICACIONES DE INTERÉS

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New Chemistry Of Bis[1,2]dithiolo[1,4]thiazines And Bis[1,2]dithiolopyrroles
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Studies On Isocyanides And Related Compounds. Synthesis Of Furan Derivatives And Their Transformation Into Indole Derivatives
Multicomponent Reactions: A Convenient Undergraduate Organic Chemistry Experiment
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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
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Bis[1,2]dithiolo[3,4-B][4',3'-E][1,4]thiazine-3,5-Dione, A Planar 1,4-Thiazine
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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
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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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