Synthesis of BEDT-TTF derivatives with carboxylic ester and amide functionalities

被引：10

作者：

Brown, RJ

Camarasa, G

Griffiths, CP

Day, P

Wallis, JD

机构：

[1] Nottingham Trent Univ, Sch Sci, Nottingham NG11 8NS, England

[2] UCL Royal Inst Great Britain, London W1S 4BS, England

来源：

TETRAHEDRON LETTERS | 2004年 / 45卷 / 26期

关键词：

organosulfur donors; hydrogen bonding; BEDT-TTF; amides;

D O I：

10.1016/j.tetlet.2004.04.176

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Synthetic routes to BEDT-TTF derivatives bearing side chain carboxylic ester and amide groups are reported. Methyl ET-ethanoate was prepared in five steps from vinylacetic acid; amide groups were installed early in the synthesis by mixed anhydride methods before the final coupling reaction. (C) 2004 Elsevier Ltd. All rights reserved.

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页码：5103 / 5107

页数：5

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