Sequential alkylation/cyclization/isomerization of ethyl 3-(o-trifluoroacetamidoaryl)-1-propargylic esters: a new route to 2-acyl- and 2-ethoxycarbonyl-3-alkenyl indoles-Reference-Cited by-同舟云学术

Sequential alkylation/cyclization/isomerization of ethyl 3-(o-trifluoroacetamidoaryl)-1-propargylic esters: a new route to 2-acyl- and 2-ethoxycarbonyl-3-alkenyl indoles

Published:2013-11 Issue:45 Volume:69 Page:9494-9498
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Ambrogio Ilaria,Arcadi Antonio,Cacchi Sandro,Fabrizi Giancarlo,Goggiamani Antonella,Marinelli Fabio

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. Palladium-Catalyzed Reactions of Propargylic Compounds in Organic Synthesis

2. Propargylic carbonates as an a1, a2 synthon in annulation reactions. A convenient synthesis of 3-methylene dihydropyran derivatives

3. New light on an old reaction: phase-transfer-catalyzed intramolecular cyclization of propargyl compounds for synthesis of indene derivatives and disubstituted benzo[b]furans

4. Palladium-Catalyzed Cyclization of Propargylic Compounds

5. Palladium-Catalyzed Synthesis of 2-(Aminomethyl)indoles from Ethyl 3-(o-Trifluoroacetamidophenyl)-1-propargyl Carbonate

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