Synthesis and reactivity of amino-substituted BEDT-TTF donors as building blocks for bifunctional materials
摘要:
The first two amino-substituted BEDT-TTF derivatives. aminomethyl-ET (AMET) and aminoethyl-ET (AEET), have been prepared; the critical step in both cases was a hetero Diels-Alder reaction with 1,3-dithiole-2,4,5-trithione. AEET shows expected reactivity towards electrophiles whereas AM ET will not react with aryl acid chlorides or sulfonyl chlorides, but amides of AMET can be produced by DCC Coupling and mixed anhydride methods. (C) 2004 Elsevier Ltd. All rights reserved.
Synthesis and reactivity of amino-substituted BEDT-TTF donors as building blocks for bifunctional materials
摘要:
The first two amino-substituted BEDT-TTF derivatives. aminomethyl-ET (AMET) and aminoethyl-ET (AEET), have been prepared; the critical step in both cases was a hetero Diels-Alder reaction with 1,3-dithiole-2,4,5-trithione. AEET shows expected reactivity towards electrophiles whereas AM ET will not react with aryl acid chlorides or sulfonyl chlorides, but amides of AMET can be produced by DCC Coupling and mixed anhydride methods. (C) 2004 Elsevier Ltd. All rights reserved.
Synthesis and reactivity of amino-substituted BEDT-TTF donors as building blocks for bifunctional materials
作者:Jon-Paul Griffiths、Anna A. Arola、Glynn Appleby、John D. Wallis
DOI:10.1016/j.tetlet.2004.02.016
日期:2004.3
The first two amino-substituted BEDT-TTF derivatives. aminomethyl-ET (AMET) and aminoethyl-ET (AEET), have been prepared; the critical step in both cases was a hetero Diels-Alder reaction with 1,3-dithiole-2,4,5-trithione. AEET shows expected reactivity towards electrophiles whereas AM ET will not react with aryl acid chlorides or sulfonyl chlorides, but amides of AMET can be produced by DCC Coupling and mixed anhydride methods. (C) 2004 Elsevier Ltd. All rights reserved.