Total syntheses of (±)-penicibilaenes A and B via intramolecular aldol condensation-Reference-Cited by-同舟云学术

Total syntheses of (±)-penicibilaenes A and B via intramolecular aldol condensation

Published:2021 Issue:21 Volume:8 Page:6063-6066
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Matsuo Rintaro¹,Watanabe Ayumu¹,Kamo Shogo¹^ORCID,Matsuzawa Akinobu¹,Sugita Kazuyuki¹^ORCID

Affiliation:

1. Department of Synthetic Medicinal Chemistry, Faculty of Pharmaceutical Sciences, Hoshi University, 2-4-41 Ebara, Shinagawa-ku, Tokyo 142-8501, Japan

Abstract

Concise total syntheses of penicibilaenes A and B were achieved via intramolecular aldol condensation and other key reactions.

Funder

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/QO/D1QO01251G

Reference31 articles.

1. Penicibilaenes A and B, Sesquiterpenes with a Tricyclo[6.3.1.01,5]dodecane Skeleton from the Marine Isolate of Penicillium bilaiae MA-267

2. Danielone, a phytoalexin from papaya fruit

3. Total synthesis of eudesmane terpenes by site-selective C–H oxidations

4. Terpenoid-Alkaloids: Their Biosynthetic Twist of Fate and Total Synthesis

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