Enantioselective Arylation of Tetrasubstituted Enamines: Access to Enantioenriched Indolenine and 1H-Indole Derivatives-Reference-Cited by-同舟云学术

Enantioselective Arylation of Tetrasubstituted Enamines: Access to Enantioenriched Indolenine and 1H-Indole Derivatives

Published:2021-01-25 Issue:3 Volume:11 Page:1827-1832
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Liang Ren-Xiao¹,Zhong Chao¹,Liu Zhi-Hong¹,Yang Miao¹,Tang Heng-Wei¹,Chen Jian-Fei¹,Yang Yun-Fang¹^ORCID,Jia Yi-Xia¹²^ORCID

Affiliation:

1. College of Chemical Engineering, State Key Laboratory Breeding Base of Green-Chemical Synthesis Technology, Zhejiang University of Technology, Chaowang Road 18#, Hangzhou 310014, China

2. State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.0c05020

Reference59 articles.

1. Cascade Reactions: A Driving Force in Akuammiline Alkaloid Total Synthesis

2. Synthesis of Spirocyclic Indolenines

3. Oxidative coupling strategies for the synthesis of indole alkaloids

4. Indole Alkaloid Synthesis Facilitated by Photoredox Catalytic Radical Cascade Reactions

5. A Novel and General Synthetic Pathway to Strychnos Indole Alkaloids: Total Syntheses of (−)-Tubifoline, (−)-Dehydrotubifoline, and (−)-Strychnine Using Palladium-Catalyzed Asymmetric Allylic Substitution

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