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[4 + 2]-Cycloadditions of a thiazol-based tricyclic 1,4-diphosphinine and a new easy 1,4-diphosphinine protection deprotection strategy.
Dalton Transactions ( IF 4 ) Pub Date : 2020-09-01 , DOI: 10.1039/d0dt02529a
Imtiaz Begum 1 , Tim Kalisch 1 , Gregor Schnakenburg 1 , Zsolt Kelemen 2 , László Nyulászi 2 , Rainer Streubel 1
Affiliation  

Diels–Alder-reactions of a thiazol-2-thione-based, tricyclic 1,4-di-phosphinine were investigated, showing that the central aromatic π-system can react with various dienophiles. The reaction with 4-phenyl-1,2,4-triazoline-3,5-dione was special as the product revealed a remarkable sensitivity towards light, thus enabling the photochemical deprotection of the tricyclic 1,4-diphosphinine.

中文翻译:

[4 + 2]-基于噻唑的三环1,4-二膦亚胺的环加成反应和一种新的简单的1,4-二膦亚胺保护脱保护策略。

研究了基于噻唑-2-硫酮的三环1,4-二次膦的狄尔斯-阿尔德反应,结果表明,中心的芳香族π-系统可以与各种亲二烯体反应。与4-苯基-1,2,4-三唑啉-3,5-二酮的反应是特殊的,因为该产物显示出对光的显着敏感性,因此使得三环1,4-二膦可以进行光化学脱保护。
更新日期:2020-09-22
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