ANODIC GLYCOSYLATION FROM ARYL THIOGLYCOSIDES

被引：58

作者：

BALAVOINE, G

GREF, A

FISCHER, JC

LUBINEAU, A

机构：

[1] Institut de Chimie Moléculaire d'Orsay, Université de Paris-Sud, F-91405 ORSAY

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 40期

关键词：

D O I：

10.1016/S0040-4039(00)97951-6

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Unprotected aryl thioglucosides undergo electrochemical oxidation in undivided cell at constant moderated potential in the presence of alcohols to give the corresponding glucosides in good yield without any self condensation. © 1990.

引用

页码：5761 / 5764

页数：4

共 11 条

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[2] ANODIC ACETAMIDOSULFENYLATION OF ALKENES
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[7] CARBOHYDRATE THIO ORTHO ESTERS .3. TRANSFORMATION TO THIOGLYCOSIDES WITH DEACTIVATED RANEY-NICKEL
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[8] ATTEMPTS TO FIND NEW ANTIMALARIALS .8. PHENYL BETA-D-GLUCOTHIOSIDES, DIPHENYL DISULFIDES, PHENYL THIOCYANATES, AND RELATED COMPOUNDS
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[9] ELECTROCHEMICAL GLYCOSYLATION METHOD
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[10] SVENSMARK B, 1983, ORGANIC ELECTROCHEMI, P520

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