SYNTHESIS FROM D-LYXONOLACTONE OF 1,4-DIDEOXY-1,4-IMINO-L-ARABINITOL, A GLUCOSIDASE INHIBITOR WITH INVITRO ANTIVIRAL ACTIVITY

被引：40

作者：

BEHLING, JR ^{[1
]}

CAMPBELL, AL ^{[1
]}

BABIAK, KA ^{[1
]}

NG, JS ^{[1
]}

MEDICH, J ^{[1
]}

FARID, P ^{[1
]}

FLEET, GWJ ^{[1
]}

机构：

[1] UNIV OXFORD,DYSON PERRINS LAB,OXFORD OX1 3QY,ENGLAND

来源：

TETRAHEDRON | 1993年 / 49卷 / 16期

关键词：

D O I：

10.1016/S0040-4020(01)90163-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Benzylidenation is the only protection required in a 7 step synthesis of the hydrochloride of 1,4-dideoxy-1,4-imino-L-arabinitol from D-lxyonolactone in an overall yield of 21%.

引用

页码：3359 / 3366

页数：8

共 45 条

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