Total syntheses of Ganoderma-derived meroterpenoids, (−)-oregonensin A, (−)-chizhine E, (−)-applanatumol U, and (−)-ent-fornicin A

Author:

Hori Kazuki1,Kamo Shogo1ORCID,Sugita Kazuyuki1ORCID

Affiliation:

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

Abstract

Total syntheses of four Ganoderma-derived meroterpenoids have been achieved with the longest linear sequence of 6–8 steps and in 21–36% overall yield by using reductive lactonization, alkylation, and sulfoxide-β-syn-elimination as key steps.

Funder

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Insights into Ganoderma fungi meroterpenoids opening a new era of racemic natural products in mushrooms;Medicinal Research Reviews;2024-01-10

2. Total synthesis of applanatumol A;Chemical Communications;2023

3. Alkylation of α-Sulfur-Containing Carbanions;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2023

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