A consecutive approach towards the stereoselective synthesis of trisubstituted THF domains

被引：15

作者：

Sagar, Ram

Reddy, L. Vijaya Raghava

Saquib, Mohammad

Kumar, Brijesh

Shaw, Arun K. ^{[1
]}

机构：

[1] Cent Drug Res Inst, Div Med & Proc Chem, Lucknow 226001, Uttar Pradesh, India

[2] Cent Drug Res Inst, Div Sophisticated Analyt Instrumentat Facil, Lucknow 226001, Uttar Pradesh, India

来源：

TETRAHEDRON-ASYMMETRY | 2006年 / 17卷 / 23期

关键词：

D O I：

10.1016/j.tetasy.2006.12.010

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

A highly efficient, consecutive approach for the construction of synthetically valued, enantiomerically pure, trisubstituted THF domains 3-10 in a stereoselective manner starting from glycal derived allylic alcohols 1a-1d under Sharpless asymmetric epoxidation (SAE) conditions is reported. The reaction involves the intramolecular asymmetric ring opening (ARO) of in situ formed enantiopure 2,3-epoxy alcohols followed by protection of the diol. (c) 2006 Elsevier Ltd. All rights reserved.

引用

页码：3294 / 3299

页数：6

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