STANNYLENE DIRECTED SELECTIVE ACYLATION OF SOME OPEN-CHAIN L-ARABINOSE DERIVATIVES

被引：24

作者：

BREDENKAMP, MW ^{[1
]}

HOLZAPFEL, CW ^{[1
]}

SWANEPOEL, AD ^{[1
]}

机构：

[1] RAND AFRIKAANS UNIV, DEPT CHEM & BIOCHEM, POB 524, JOHANNESBURG 2000, SOUTH AFRICA

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 19期

关键词：

D O I：

10.1016/S0040-4039(00)94692-6

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Controlled mono-2- or -4-acylation of open-chain L-arabinose derivatives is achieved by terminal group manipulation and dibutylstannylene oxide activation. The method was used for the preparation of a 4-mesyl-Larabinose derivative which was converted into a thioxylose synthon. © 1990.

引用

页码：2759 / 2762

页数：4

共 14 条

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