Total synthesis of enokipodins A-D and cuparene-1,4-diol

被引：0

作者：

Srikrishna, A. ^{[1
]}

Rao, M. Srinivasa ^{[1
]}

机构：

[1] Indian Inst Sci, Dept Organ Chem, Bangalore 560012, Karnataka, India

来源：

INDIAN JOURNAL OF CHEMISTRY SECTION B-ORGANIC CHEMISTRY INCLUDING MEDICINAL CHEMISTRY | 2010年 / 49卷 / 10期

关键词：

Enokipodins; cuparenes; RCM reaction; Claisen rearrangement; sesquiterpenes; CUPARENE-TYPE SESQUITERPENES; OLEFIN METATHESIS; MYCELIAL CULTURE; (+/-)-ALPHA-HERBERTENOL; (+/-)-ENOKIPODIN-A; REARRANGEMENT;

D O I：

暂无

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A Claisen rearrangement and RCM reaction based sequence has been developed for total synthesis of the antifungal sesquiterpenes enokipodins A-D and cuparene-1,4-diol starting from 2,5-dimethoxy-4-methylhydroquinone.

引用

页码：1363 / 1371

页数：9

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