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Base-controlled selective cleavage of the C–F bond of difluorocarbene for the divergent assembly of indolizines
Organic Chemistry Frontiers ( IF 4.6 ) Pub Date : 2024-06-12 , DOI: 10.1039/d4qo00801d
Chun-Yan Wu 1 , Xiang-Long Chen 1 , Dong-Sheng Yang 1 , Yong-Xing Tang 1 , Li-Sheng Wang 1 , Yan-Dong Wu 1 , Shi-Yi Zhuang 2 , An-Xin Wu 1, 3
Affiliation  

A [3 + 1 + 1] cascade annulation reaction for the divergent construction of trisubstituted indolizines using sulfoxonium ylides, BrCF2CO2Me and pyridinium salts as readily available substrates has been developed. By changing the reaction conditions, this metal-free process realized selective cleavage of one or two C–F bonds of difluorocarbene and let it act as a C or CF source. Further transformation of the product presented the practicality of this reaction.

中文翻译:


碱基控制选择性裂解二氟卡宾的 C-F 键以实现中氮茚的不同组装



开发了一种 [3 + 1 + 1] 级联环化反应,使用亚锍叶立德、BrCF 2 CO 2 Me 和吡啶鎓盐作为容易获得的底物来不同地构建三取代中氮茚。通过改变反应条件,这种无金属工艺实现了二氟卡宾的一个或两个C-F键的选择性断裂,并使其充当C或CF源。产物的进一步转化表明了该反应的实用性。
更新日期:2024-06-12
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