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Visible-Light-Mediated ipso-Carbosulfonylation of Alkynes: Synthesis of 3-Sulfonylspiro[4,5]trienones from Propiolamides and Sulfonyl Chlorides under Transition-Metal-Free Conditions
Synlett ( IF 2 ) Pub Date : 2018-09-07 , DOI: 10.1055/s-0037-1609948
Yu Liu , Quan Zhou 1 , Qiao-Lin Wang , Bi-Quan Xiong , Pan-Liang Zhang , Chang-An Yang , Yan-Xia Gong , Jing Liao
Affiliation  

An efficient and convenient strategy to synthesize diverse 3-sulfonylspiro[4,5]trienones has been developed. This ipso-carbosulfonylation of alkynes proceeds by visible-light catalysis under transition-metal-free conditions and represents a new sulfonylation and ipso-cyclization of alkynes. In this transformation, the O atom in the newly generated carbonyl is derived from H2O and it features a broad substrates scope, especially for alkyl propiolamides and aliphatic sulfonyl chlorides.

中文翻译:

可见光介导的炔烃 ipso-Carbosulfonylation:在无过渡金属条件下由丙吡胺和磺酰氯合成 3-磺酰基螺[4,5]三烯酮

已开发出一种高效便捷的合成多种 3-磺酰基螺[4,5] 三烯酮的策略。这种炔烃的同位碳磺酰化在无过渡金属条件下通过可见光催化进行,代表了炔烃的新磺酰化和同位环化。在这种转化中,新生成的羰基中的 O 原子来源于 H2O,它具有广泛的底物范围,特别是对于烷基丙酰胺和脂肪族磺酰氯。
更新日期:2018-09-07
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