An aza-payne rearrangement-epoxide ring opening reaction of 2-aziridinemethanols in a one-pot manner: A regio- and stereoselective synthetic route to diastereomerically pure N-protected 1,2-amino alcohols

被引：29

作者：

Ibuka, T ^{[1
]}

Nakai, K ^{[1
]}

Akaji, M ^{[1
]}

Tamamura, H ^{[1
]}

Fujii, N ^{[1
]}

Yamamoto, Y ^{[1
]}

机构：

[1] TOHOKU UNIV, FAC SCI, DEPT CHEM, SENDAI, MIYAGI 980, JAPAN

来源：

TETRAHEDRON | 1996年 / 52卷 / 36期

关键词：

D O I：

10.1016/0040-4020(96)00682-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A regio- and stereoselective synthetic route to diastereomerically pure 1,2-amino alcohols via a one-pot aza-Payne rearrangement - epoxide ring opening reaction of 2-aziridinemethanols is reported. Copyright (C) 1996 Elsevier Science Ltd

引用

页码：11739 / 11752

页数：14

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