Stereloselective synthesis of the lituarine tricyclic spiroacetal

被引：46

作者：

Robertson, J ^{[1
]}

Meo, P ^{[1
]}

Dallimore, JWP ^{[1
]}

Doyle, BM ^{[1
]}

Hoarau, C ^{[1
]}

机构：

[1] Univ Oxford, Dept Chem, Chem Res Lab, Oxford OX1 3TA, England

来源：

ORGANIC LETTERS | 2004年 / 6卷 / 21期

关键词：

D O I：

10.1021/ol0483955

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Oxidative cyclizations of 2-(4-hydroxybutyl)furan derivatives provide spirobutenolide acetals directly; on the basis of this methodology, we describe an asymmetric synthesis of a tricyclic spirobutenolide precursor to the C(7-18) fragment common to lituarines A-C.

引用

页码：3861 / 3863

页数：3

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