An expedient route to p-tert-butylthiacalix[4]arene 1,3-diethers via Mitsunobu reactions

被引：62

作者：

Bitter, I ^{[1
]}

Csokai, V ^{[1
]}

机构：

[1] Budapest Univ Technol & Econ, Dept Organ Chem Technol, H-1521 Budapest, Hungary

来源：

TETRAHEDRON LETTERS | 2003年 / 44卷 / 11期

基金：

匈牙利科学研究基金会;

关键词：

thiacalix[4]arenes; O-alkylation; mitsunobu reaction;

D O I：

10.1016/S0040-4039(03)00285-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Regioselective distal dialkylation of p-tert-butylthiacalix[4]arene with alcohols was performed under the Mitsunobu protocol using the DEAD/TPP system. The method provides a versatile tool for obtaining 1,3-diethers with different functional groups in the alkyl chains. (C) 2003 Elsevier Science Ltd. All rights reserved.

引用

页码：2261 / 2265

页数：5

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