Base-promoted domino reaction for the synthesis of 2,3-disubstituted indoles from 2-aminobenzaldehyde/2-amino aryl ketones, tosylhydrazine, and aromatic aldehydes-Reference-Cited by-同舟云学术

Base-promoted domino reaction for the synthesis of 2,3-disubstituted indoles from 2-aminobenzaldehyde/2-amino aryl ketones, tosylhydrazine, and aromatic aldehydes

Published:2016-08 Issue:32 Volume:72 Page:4821-4826
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Wu Yan-Dong,Ma Jun-Rui,Shu Wen-Ming,Zheng Kai-Lu,Wu An-Xin

Funder

National Natural Science Foundation of China

Central China Normal University

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference96 articles.

1. For selected examples, see:

2. Brønsted Acid Mediated Cyclization of Enaminones. Rapid and Efficient Access to the Tetracyclic Framework of the Strychnos Alkaloids

3. Katalytische Funktionalisierung von Indolen in einer neuen Dimension

4. Catalytic Functionalization of Indoles in a New Dimension

5. Enantiospecific Total Synthesis of the Hapalindoles, Fischerindoles, and Welwitindolinonesviaa Redox Economic Approach

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