Asymmetric total syntheses of five pyrrole-type <i>Stemona</i> alkaloids-Reference-Cited by-同舟云学术

Asymmetric total syntheses of five pyrrole-type Stemona alkaloids

Published:2022 Issue:14 Volume:9 Page:3818-3822
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Wang Xiaodong¹,Shi Tao¹^ORCID,Yin Gaofeng¹,Wang Yuqing¹,Li Zhao¹,Wang Zhen¹²^ORCID

Affiliation:

1. School of Pharmacy, Lanzhou University, No. 199 West Donggang Road, Lanzhou, China

2. School of Pharmaceutical Science, Hengyang Medical School, University of South China, Hengyang 421001, Hunan, China

Abstract

The asymmetric total syntheses of five pyrrole-type Stemona alkaloids were accomplished, among which 3-n-butylneostemonine and bisdehydroneostemonine were synthesized for the first time, and the NMR data of bisdehydroneostemonine were revised.

Funder

Natural Science Foundation for Distinguished Young Scholars of Gansu Province

Recruitment Program of Global Experts

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QO/D2QO00456A

Reference41 articles.

1. Recent progress in the chemistry of the Stemona alkaloids

2. Structural Relationships, Distribution and Biological Activities ofStemonaAlkaloids

3. The chemistry of Stemona alkaloids: An update

4. Structural classification and biological activities of Stemona alkaloids

5. Pyrrole Strategy for the γ-Lactam-Containing Stemona Alkaloids: (±)Stemoamide, (±)Tuberostemoamide, and (±)Sessilifoliamide A

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