An Asymmetric Synthesis of (+)-Isostrychnine Based on Catalytic Asymmetric Tandem Double Michael Addition-Reference-Cited by-同舟云学术

An Asymmetric Synthesis of (+)-Isostrychnine Based on Catalytic Asymmetric Tandem Double Michael Addition

Published:2021-07-02 Issue:14 Volume:23 Page:5476-5479
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Pengyan¹,Chen Junhan¹,He Weigang¹,Song Jiacheng¹,Song Hengqian¹,Wei Hongbo¹,Xie Weiqing¹²^ORCID

Affiliation:

1. Shaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F University, 22 Xinong Road, Yangling, Shaanxi 712100, China

2. Key Laboratory of Botanical Pesticide R&D in Shaanxi Province, Yangling, Shaanxi 712100, China

Funder

Northwest A and F University

National Natural Science Foundation of China

Shaanxi Government

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c01828

Reference52 articles.

1. Recent progress in the total synthesis of Strychnos alkaloids

2. 198. Strychnine and brucine. Part XLII. Constitution of the neo-series of bases and their oxidation products

3. THE STRUCTURE OF STRYCHNINE

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