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Assembly of fully substituted 2,5-dihydrothiophenes via a novel sequential multicomponent reaction†
Organic Chemistry Frontiers ( IF 5.4 ) Pub Date : 2018-05-21 00:00:00 , DOI: 10.1039/c8qo00343b
Giacomo Mari 1, 2, 3, 4, 5 , Michele Verboni 1, 2, 3, 4, 5 , Lucia De Crescentini 1, 2, 3, 4, 5 , Gianfranco Favi 1, 2, 3, 4, 5 , Stefania Santeusanio 1, 2, 3, 4, 5 , Fabio Mantellini 1, 2, 3, 4, 5
Affiliation  

A new and efficient synthesis of fully substituted 2,5-dihydrothiophenes by a sequential one-pot four component reaction between primary amines, β-ketoesters, aryl isothiocyanates and 1,2-diaza-1,3-dienes (DDs) is reported. A careful selection of the starting materials enables the choice of up to six different variations in the architecture of the final products. Furthermore, the acidic treatment of the so-obtained 2,5-dihydrothiophenes furnishes the corresponding 5-amino thiophene-2,4-dicarboxylates.

中文翻译:

通过新颖的顺序多组分反应 组装完全取代的2,5-二氢噻吩

据报道,通过伯胺,β-酮酸酯,芳基异硫氰酸酯和1,2-二氮杂-1,3-二烯(DDs)之间的顺序一锅四组分反应,可以有效地合成完全取代的2,5-二氢噻吩。仔细选择原材料,可以在最终产品的结构中选择多达六个不同的变化。此外,如此获得的2,5-二氢噻吩的酸性处理提供了相应的5-氨基噻吩-2,4-二羧酸酯。
更新日期:2018-05-21
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