Aminative rearrangement of 2-alkoxy-3,4-dihydro-2H-pyrans:: a novel stereocontrolled route to substituted pyrrolidines

被引：16

作者：

Armstrong, A ^{[1
]}

Cumming, GR

Pike, K

机构：

[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AZ, England

[2] AstraZeneca, CVGI Chem, Macclesfield SK10 4TG, Cheshire, England

来源：

CHEMICAL COMMUNICATIONS | 2004年 / 07期

关键词：

D O I：

10.1039/b316554j

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Aziridination of 2-alkoxy-3,4-dihydro-2H-pyrans leads to rearrangement and stereocontrolled formation of 5-alkoxypyrrolidines which may be reduced to pyrrolidines or allylated stereoselectively.

引用

页码：812 / 813

页数：2

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