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Tetracyanoethylene as a building block in the facile synthesis of heteroyl-tetrasubstituted thiazoles
Monatshefte für Chemie - Chemical Monthly ( IF 1.7 ) Pub Date : 2020-09-10 , DOI: 10.1007/s00706-020-02669-4 Alaa A. Hassan , Ashraf A. Aly , Nasr K. Mohamed , Lamiaa E. Abd El-Haleem , Stefan Bräse , Martin Nieger
中文翻译:
四甲基氨基乙烯是轻松合成杂基四取代噻唑的基础
更新日期:2020-09-10
Monatshefte für Chemie - Chemical Monthly ( IF 1.7 ) Pub Date : 2020-09-10 , DOI: 10.1007/s00706-020-02669-4 Alaa A. Hassan , Ashraf A. Aly , Nasr K. Mohamed , Lamiaa E. Abd El-Haleem , Stefan Bräse , Martin Nieger
Abstract
The transformation of N-substituted 2-heteroylthiosemicarbazides to N-(2-substituted imino)-4-amino-5-cyanothiazol-3(2H)-3-yl)-heteroyl-2-carboxamides was achieved via the reaction with tetracyanoethylene, which is used as a building block in this transformation. The structures of the products have been confirmed unambiguously by single-crystal X-ray structure analysis. A rationale for the formation of the products is presented.
Graphic abstract
中文翻译:
四甲基氨基乙烯是轻松合成杂基四取代噻唑的基础
摘要
通过与四氰基乙烯反应,实现了N-取代的2-杂基硫代氨基脲向N-(2-取代的亚氨基)-4-氨基-5-氰基噻唑-3 (2 H)-3-基)-杂基-2-羧酰胺的转化。 ,它在此转换中用作构建块。通过单晶X射线结构分析已明确确认了产物的结构。提出了形成产品的基本原理。