A chemoenzymatic synthesis of the 12-membered macrolide (-)-cladospolide A

被引：24

作者：

Banwell, MG ^{[1
]}

Jolliffe, KA ^{[1
]}

Loong, DTJ ^{[1
]}

McRae, KJ ^{[1
]}

Vounatsos, F ^{[1
]}

机构：

[1] Australian Natl Univ, Inst Adv Studies, Res Sch Chem, Canberra, ACT 0200, Australia

来源：

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 2002年 / Royal Society of Chemistry卷 / 01期

关键词：

D O I：

10.1039/b110018a

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The enantiomerically pure cis-1,2-dihydrocatechol 7, which is obtained by microbial oxidation of chlorobenzene, has been converted, via a sequence of reactions including ring-closing metathesis and Yamaguchi lactonisation steps, into the natural product (-)-cladospolide A (1).

引用

页码：22 / 25

页数：4

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