STEREOSELECTIVE CYCLOADDITIONS OF CHIRAL ACYL-NITROSO COMPOUNDS - HYDROLYTIC REACTIONS OF A CYCLOPENTADIENE ADDUCT

被引：22

作者：

MUXWORTHY, JP ^{[1
]}

WILKINSON, JA ^{[1
]}

PROCTER, G ^{[1
]}

机构：

[1] UNIV SALFORD,DEPT CHEM & APPL CHEM,SALFORD M5 4WT,LANCS,ENGLAND

来源：

TETRAHEDRON LETTERS | 1995年 / 36卷 / 41期

关键词：

D O I：

10.1016/0040-4039(95)01525-6

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Treatment of the adduct between the acyl nitroso intermediate derived from (R)-alpha-hydroxyphenylacetohydroxamic acid and cyclopentadiene, 1, with dilute aqueous acid provides a high yield of the cyclopentene 2 hydrochloride, suitable for further synthetically useful transformations.

引用

页码：7535 / 7538

页数：4

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