Total Synthesis of (−)‐Lepadin F based on a Stereoselective Diels–Alder Reaction Controlled by a Ketolactone‐type Dienophile-Reference-Cited by-同舟云学术

Total Synthesis of (−)‐Lepadin F based on a Stereoselective Diels–Alder Reaction Controlled by a Ketolactone‐type Dienophile

Published:2021-01-29 Issue:12 Volume:27 Page:4141-4149
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Gu He¹,Hu Yue¹,Jia Yuanliang¹,Zhou Qin¹,Luo Guiyin¹,Chen Xiaochuan¹^ORCID

Affiliation:

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

Funder

National Natural Science Foundation of China

Department of Science and Technology of Sichuan Province

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202004778

Reference60 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. Lepadins I–K, 3-O-(3′-Methylthio)acryloyloxy-decahydroquinoline Esters from a Bahamian Ascidian Didemnum sp. Assignment of Absolute Stereostructures

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