Preparation and conversion of chiral O-isopropylidene-protected 4-aminocyclohexenol to various key intermediates toward narcissus alkaloids

被引：13

作者：

Elango, S ^{[1
]}

Wang, YC ^{[1
]}

Cheng, CL ^{[1
]}

Yan, TH ^{[1
]}

机构：

[1] Natl Chung Hsing Univ, Dept Chem, Taichung 400, Taiwan

来源：

TETRAHEDRON LETTERS | 2002年 / 43卷 / 20期

关键词：

D O I：

10.1016/S0040-4039(02)00543-9

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Enantiomerically pure 4-amino-5,6-O-isopropylidenedioxycyclohex-2-en-1-ol, conveniently prepared by the union of O-isopropylidenedioxycyclohexadiene with camphor-based chloronitroso ester, was employed in the synthesis of versatile key intermediates toward narcissus alkaloids. (C) 2002 Elsevier Science Ltd. All rights reserved.

引用

页码：3757 / 3759

页数：3

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