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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >[4+2]-Cycloadditions of a thiazol-based tricyclic 1,4-diphosphinine and a new easy 1,4-diphosphinine protection deprotection strategy
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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

机译:[4 + 2] -cycloaddition的噻唑基三环素1,4-二膦碱和一种新的易1,4-二膦保护脱保护策略

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摘要

Diels-Alder-reactions of a thiazol-2-thione-based, tricyclic 1,4-di-phosphinine were investigated, showing that the central aromatic It-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.
机译:研究了基于噻唑-2-尖端的三环1,4-二膦素的Diels-酰胺反应,表明中央芳族IT系统可以与各种辅酶素反应。 与4-苯基-1,2,4-三唑啉-3,5-二酮的反应特殊,因为产品揭示了对光的显着敏感性,因此能够使三环1,4-二磷素的光化学脱保护。

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