A Stereoselective Approach toward (−)-Lepadins A–C-Reference-Cited by-同舟云学术

A Stereoselective Approach toward (−)-Lepadins A–C

Published:2017-09-19 Issue:19 Volume:19 Page:5372-5375
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Li Xiong¹,Hu Lingling¹,Jia Junhao¹,Gu He¹,Jia Yuanliang¹,Chen Xiaochuan¹^ORCID

Affiliation:

1. Key Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, People’s Republic of China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b02647

Reference40 articles.

1. Lepadin A, A decahydroquinoline alkaloid from the tunicate Clavelina lepadiformis

2. Cytotoxic alkaloids from the flatworm Prostheceraeus villatus and its tunicate prey Clavelina lepadiformis

3. Lepadins D−F: Antiplasmodial and Antitrypanosomal Decahydroquinoline Derivatives from the Tropical Marine Tunicate Didemnum sp.

4. Lepadins F−H, New cis-Decahydroquinoline Alkaloids from the Australian Ascidian Aplidium tabascum

5. Marine Alkaloids (-)-Pictamine and (-)-Lepadin B Block Neuronal Nicotinic Acetylcholine Receptors

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