Gold-catalyzed benzannulations of 2-alkenylindoles with alkynes: a protecting-group-free regioselective approach to carbazoles-Reference-Cited by-同舟云学术

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Gold-catalyzed benzannulations of 2-alkenylindoles with alkynes: a protecting-group-free regioselective approach to carbazoles

Published:2024 Issue:40 Volume:60 Page:5326-5329
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Amin Pathan Mosim¹,Wang Weilin¹,Wang Chao¹,Zhou Junrui¹,Wang Youliang¹^ORCID

Affiliation:

1. School of Chemistry, MOE Key Laboratory for Nonequilibrium Synthesis and Modulation of Condensed Matter, Xi’an Key Laboratory of Sustainable Energy Materials Chemistry, Xi’an Jiaotong University (XJTU), Xi’an, 710049, China

Abstract

A gold(i)-catalyzed protecting-group-free benzannulation approach to functionalized NH-carbazoles was accomplished via the hydroarylation of alkynes with 2-alkenylindoles.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CC/D4CC00176A

Reference34 articles.

1. Isolation and Synthesis of Biologically Active Carbazole Alkaloids

2. Biological potential of carbazole derivatives

3. On the constitution of murrayanine, a carbazole derivative isolated from Murraya koenigii Spreng

4. Phase II study of elliptinium acetate salvage treatment of advanced breast cancer

5. Identification and Characterization of Carprofen as a Multitarget Fatty Acid Amide Hydrolase/Cyclooxygenase Inhibitor

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