A stereocontrolled synthetic route to anti-β-amino alcohols

被引：9

作者：

Kang, SH ^{[1
]}

Hwang, YS

Youn, JH

机构：

[1] Korea Adv Inst Sci & Technol, Sch Mol Sci BK21, Dept Chem, Taejon 305701, South Korea

[2] Sun Moon Univ, Dept Chem Engn, Chungnam 336840, South Korea

来源：

TETRAHEDRON LETTERS | 2001年 / 42卷 / 43期

关键词：

D O I：

10.1016/S0040-4039(01)01611-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A physiologically indispensable beta -amino hydroxy functionality has been constructed with complete anti-stereoselectivity by intramolecular iodoamidation of (Z)-olefinic homoallylic trichloroacetimidates 4-6, 18, 20, 30 and 32, which comprise bulky substituents at the vinylic positions. (C) 2001 Elsevier Science Ltd. All rights reserved.

引用

页码：7599 / 7603

页数：5

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