General Approach To Construct Azepino[2,3-b:4,5-b′]diindoles, Azocino[2,3-b:4,5-b′]diindoles, and Azonino[2,3-b:4,5-b′]diindoles via Rh(II)-Catalyzed Reactions of 3-Diazoindolin-2-imines with 3-(Bromoalkyl)indoles-Reference-Cited by-同舟云学术

General Approach To Construct Azepino[2,3-b:4,5-b′]diindoles, Azocino[2,3-b:4,5-b′]diindoles, and Azonino[2,3-b:4,5-b′]diindoles via Rh(II)-Catalyzed Reactions of 3-Diazoindolin-2-imines with 3-(Bromoalkyl)indoles

Published:2019-07-01 Issue:15 Volume:84 Page:9561-9569
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Sheng Guorong¹,Li Zhenmin¹,Mao Jianming¹,Lu Ping¹^ORCID,Wang Yanguang¹^ORCID

Affiliation:

1. Department of Chemistry, Zhejiang University, Hangzhou 310027, P. R. China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b01169

Reference26 articles.

1. Sesquiterpenyl indoles

2. Simple indole alkaloids and those with a non-rearranged monoterpenoid unit

3. Indoles in Multicomponent Processes (MCPs)

4. Structure–Activity Relationship Studies of Indole-Based Compounds as Small Molecule HIV-1 Fusion Inhibitors Targeting Glycoprotein 41

5. General Approach for Preparing Epidithiodioxopiperazines from Trioxopiperazine Precursors: Enantioselective Total Syntheses of (+)- and (−)-Gliocladine C, (+)-Leptosin D, (+)-T988C, (+)-Bionectin A, and (+)-Gliocladin A

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