Highly Regioselective Synthesis of 2‐Acylindolines through Cobalt‐Catalyzed C−H Activation/[3+2] Annulation of Aniline Derivatives and Acrylates-Reference-Cited by-同舟云学术

Highly Regioselective Synthesis of 2‐Acylindolines through Cobalt‐Catalyzed C−H Activation/[3+2] Annulation of Aniline Derivatives and Acrylates

Published:2022-11-24 Issue:24 Volume:364 Page:4421-4426
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv Synth Catal

Author:

Tian Xun¹^ORCID,Pan Ailin¹,Du Ya¹,Zhang Lening¹,Qin Cuirong¹,Duan Shengzu¹²,Yang Lijuan²,Yang Xiaodong¹^ORCID

Affiliation:

1. Key Laboratory of Medicinal Chemistry for Natural Resource Ministry of Education Yunnan Provincial Center for Research & Development of Natural Products School of Pharmacy Yunnan University Kunming 650500 People's Republic of China

2. School of Chemistry and Environment Yunnan Minzu University Kunming 650500 People's Republic of China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202200965

Reference54 articles.

2. Chemistry and biology of monoterpene indole alkaloid biosynthesis

3. Discovery of a P450-catalyzed step in vindoline biosynthesis: a link between the aspidosperma and eburnamine alkaloids

4. Indoles — A promising scaffold for drug development

5. Indole: A privileged scaffold for the design of anti-cancer agents

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