Facile synthesis of 5H-benzo[b]carbazol-6-yl ketones via sequential reaction of Cu-catalyzed Friedel–Crafts alkylation, iodine-promoted cyclization, nucleophilic substitution and aromatization-Reference-Cited by-同舟云学术

Facile synthesis of 5H-benzo[b]carbazol-6-yl ketones via sequential reaction of Cu-catalyzed Friedel–Crafts alkylation, iodine-promoted cyclization, nucleophilic substitution and aromatization

Published:2014 Issue:35 Volume:12 Page:6806-6811
ISSN:1477-0520
Container-title:Org. Biomol. Chem.
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wu Jing¹²³,Wang Dongping¹²³,Wang Haolong¹²³,Wu Fan¹²³,Li Xincheng¹²³,Wan Boshun¹²³

Affiliation:

1. Dalian Institute of Chemical Physics

2. Chinese Academy of Sciences

3. Dalian 116023, China

Abstract

A convenient method to access 5H-benzo[b]carbazol-6-yl ketones from indoles and 2-(2-(alkynyl)benzylidene)malonates has been developed.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/OB/C4OB00815D

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