STEREOSPECIFIC CYCLIZATION OF VINYL ETHER ALCOHOLS - FACILE SYNTHESIS OF (-)-LARDOLURE

被引：45

作者：

KAINO, M ^{[1
]}

NARUSE, Y ^{[1
]}

ISHIHARA, K ^{[1
]}

YAMAMOTO, H ^{[1
]}

机构：

[1] NAGOYA UNIV,DEPT APPL CHEM,CHIKUSA KU,NAGOYA 46401,JAPAN

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1990年 / 55卷 / 23期

关键词：

D O I：

10.1021/jo00310a007

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

: An efficient and stereospecific ring formation from unsaturated alcohols, which in turn are prepared by regio- and stereospecific ring opening of acetals, is described. © 1990, American Chemical Society. All rights reserved.

引用

页码：5814 / 5815

页数：2

共 19 条

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[7] 7-MEMBERED RINGS VIA SILYL ENOL ETHER PARTICIPATION IN OLEFIN CYCLIZATION - ANTI-MARKOWNIKOFF CYCLIZATION IN BIOMIMETIC TERPENE SYNTHESIS
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[9] RESOLUTION OF KETONES VIA CHIRAL ACETALS - KINETIC APPROACH
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