DECONJUGATIVE ALDOL-CYCLIZATION SEQUENCE FOR THE CONSTRUCTION OF SUBSTITUTED 2-METHOXYTETRAHYDROFURANS

被引：12

作者：

GALATSIS, P

MANWELL, JJ

机构：

[1] Department of Chemistry and Biochemistry, University of Guelph, Guelph

来源：

TETRAHEDRON LETTERS | 1995年 / 36卷 / 45期

关键词：

D O I：

10.1016/0040-4039(95)01798-M

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

We have shown that the conditions of iodine-pyridine provides a stereoselective method of cyclizing homoallylic alcohols derived from the deconjugative aldol reaction of methyl (E)-4-methoxy-3-butenoate.

引用

页码：8179 / 8182

页数：4

共 15 条

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