DIASTEREOSELECTIVE ROUTES TO ENDO AND EXO ETHYL 1-AZABICYCLO[2.2.1]HEPT-3-YL CARBOXYLATES

被引：13

作者：

ORLEK, BS

WADSWORTH, H

WYMAN, P

HADLEY, MS

机构：

[1] SmithKline Beecham Pharmaceuticals, Medicinal Research Centre, Harlow, Essex CM19 5AD, Coldharbour Road, The Pinnacles

来源：

TETRAHEDRON LETTERS | 1991年 / 32卷 / 09期

关键词：

D O I：

10.1016/S0040-4039(00)92055-0

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Diastereoselective routes to endo and exo ethyl 1-azabicyclo[2.2.1]hept-3-yl-carboxylates (1) and (2) based on the hydrogen bromide cleavage of the isomeric [4.3.0] bicyclic cis fused lactones (3) and (4) are described.

引用

页码：1241 / 1244

页数：4

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