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黄伞素 L,云芝中一种倍半萜代谢产物:分离、结构阐明和不对称全合成。

Phellilane L, Sesquiterpene Metabolite of Phellinus linteus: Isolation, Structure Elucidation, and Asymmetric Total Synthesis.

机构信息

School of Pharmacy, Tokyo University of Pharmacy and Life Sciences , 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan.

School of Pharmacy, Kitasato University , 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641, Japan.

出版信息

J Org Chem. 2017 Dec 1;82(23):12377-12385. doi: 10.1021/acs.joc.7b02141. Epub 2017 Nov 9.

Abstract

A new cyclopropane-containing sesquiterpenoid, phellilane L (1), was isolated from the medicinal mushroom Phellinus linteus ("Meshimakobu" in Japanese), a member of the Hymenochaetaceae family and a well-known fungus that is widely used in East Asia. The planar structure of 1 was determined on the basis of spectroscopic analysis. The authors achieved the first total synthesis of 1. Our protecting group-free synthesis features a highly stereoselective one-pot synthesis involving an intermolecular alkylation/cyclization/lactonization strategy for construction of the key cyclopropane-γ-lactone intermediate. Additionally, our synthesis determined the absolute configuration of phellilane L (1).

摘要

一种新的含环丙烷的倍半萜,phellilane L(1),从药用蘑菇 Phellinus linteus(在日语中称为“Meshimakobu”)中分离出来,该蘑菇属于 Hymenochaetaceae 科,是一种在东亚广泛使用的知名真菌。1 的平面结构是基于光谱分析确定的。作者实现了 1 的首次全合成。我们的无保护基团合成采用高立体选择性的一锅合成,涉及分子间烷基化/环化/内酯化策略,用于构建关键的环丙烷-γ-内酯中间体。此外,我们的合成确定了 phellilane L(1)的绝对构型。

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