Asymmetric synthesis of cis-aminochromanol

被引：18

作者：

Hansen, KB ^{[1
]}

Rabbat, P ^{[1
]}

Springfield, SA ^{[1
]}

Devine, PN ^{[1
]}

Grabowski, EJJ ^{[1
]}

Reider, PJ ^{[1
]}

机构：

[1] Merck & Co Inc, Dept Proc Res, Rahway, NJ 07765 USA

来源：

TETRAHEDRON LETTERS | 2001年 / 42卷 / 50期

关键词：

D O I：

10.1016/S0040-4039(01)01907-4

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

An efficient asymmetric synthesis of cis-aminochromanol was achieved in seven steps. The absolute stereochemistry of cis-aminochromanol was derived from (salen)Co(III)-catalyzed phenol opening of methyl glycidate. (C) 2001 Elsevier Science Ltd. All rights reserved.

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页码：8743 / 8745

页数：3

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