THE SYNTHESIS OF 7-CARBONYL HOMOLOGS OF 1-DEOXYNOJIRIMYCIN

被引：21

作者：

KILONDA, A ^{[1
]}

COMPERNOLLE, F ^{[1
]}

TOPPET, S ^{[1
]}

HOORNAERT, GJ ^{[1
]}

机构：

[1] KATHOLIEKE UNIV LEUVEN,SYNTH ORGAN LAB,B-3001 LOUVAIN,BELGIUM

来源：

TETRAHEDRON LETTERS | 1994年 / 35卷 / 48期

关键词：

D O I：

10.1016/0040-4039(94)88424-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A 3,4;5,6-di-O-isopropylidene salt derivative of 1-amino-1-deoxy-D-glucitol was transformed to N-Boc protected (5,6)-alpha,beta-unsaturated 7-carbonyl compounds. Conversion to the title piperidine products proceeded via deprotection and intramolecular 1,4-addition of the amino group.

引用

页码：9047 / 9050

页数：4

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