STEREOCONTROLLED FORMATION OF FUNCTIONALIZED ERYTHRO-1,2-DIOLS VIA HYDROBORATION OF 2-ALKYL-4,5-DIHYDROFURANS

被引：6

作者：

AMOUROUX, R

SLASSI, A

SALUZZO, C

机构：

[1] Laboratoire de Chimie Organique Physique et Synthétique, associé au CNRS. Université Claude Bernard, 69622 Villeurbanne, Lyon I, 43 Boulevard du

来源：

HETEROCYCLES | 1993年 / 36卷 / 09期

关键词：

D O I：

10.3987/COM-93-6428

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

trans-2-Alkyl-3-hydroxytetrahydrofurans, prepared by the stereospecific hydroboration / oxidation reaction of 2-alkyl-4,5-dihydrofurans, were regioselectively cleaved with (CH3)3SiCl / NaI to afford 1-iodo-erythro-3,4-diols in CH3CN or the corresponding acetonide derivatives in CH3COCH3.

引用

页码：1965 / 1969

页数：5

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