Synthesis of 3-iodothiophenes via iodocyclization of (Z)-thiobutenynes

被引:28
作者
Santana, Amanda S. [1 ,2 ]
Carvalho, Diego B. [1 ,2 ]
Cassemiro, Nadla S. [1 ,2 ]
Viana, Luiz H. [1 ,2 ]
Hurtado, Gabriela R. [1 ,2 ]
Amaral, Marcos S. [1 ,2 ]
Kassab, Najla M. [1 ,2 ]
Guerrero, Palimecio G., Jr. [3 ]
Barbosa, Sandro L. [4 ]
Dabdoub, Miguel J. [5 ]
Baroni, Adriano C. M. [1 ,2 ]
机构
[1] Univ Fed Mato Grosso do Sul, UFMS, Ctr Ciancias Biol & Saude, LASQUIM Lab Sintese & Quim Med, BR-79070900 Campo Grande, MS, Brazil
[2] Univ Fed Mato Grosso do Sul, UFMS, Inst Quim, BR-79070900 Campo Grande, MS, Brazil
[3] Univ Tecnol Fed Parana, UTFPR, DAQBi, Dept Quim & Biol, BR-80230901 Curitiba, PR, Brazil
[4] Univ Fed Vale Jequitinhonha & Mucuri, Dept Farm & Bioquim, BR-39100000 Diamantina, MG, Brazil
[5] Univ Sao Paulo, Dept Quim, BR-14040901 Ribeirao Preto, SP, Brazil
关键词
(Z)-Thiobutenynes; Iodocyclization; 3-Iodothiophenes; Sonogashira cross coupling; ONE-POT SYNTHESIS; ELECTROPHILIC CYCLIZATION; VINYLIC TELLURIDES; THIOPHENES; PRECURSORS;
D O I
10.1016/j.tetlet.2013.10.118
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A simple synthesis of 3-iodothiophenes was demonstrated using a wide range of (Z)-thioenynes. The key step in the iodocyclofunctionalization was the selective reduction of the triple bond in (Z)-thioenynes by the addition of iodine as an electrophilic agent. The 3-iodothiophenes were obtained in good to excellent yields of 61-92%. The 3-iodothiophenes were used as substrates in Sonogashira cross-coupling reactions to obtain thiophene acetylenes. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:52 / 55
页数:4
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