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Modular access to formamide-tethered α-halo ynones via the deconstructive oxo-halogenation of readily available α-alkynyl eneformamides
Tetrahedron Letters ( IF 1.8 ) Pub Date : 2020-03-11 , DOI: 10.1016/j.tetlet.2020.151821
Timothy K. Beng , Abdikani Omar Farah

Herein, we describe a chemoselective, regioselective, modular, and efficient deconstructive oxo-halogenation strategy, which skeletally remodels readily available cyclic α-alkynyl eneformamides into formamide-tethered α-halo ynones. This scaffold-hopping transformation furnishes diverse architectures that would be challenging to achieve through traditional disconnections.



中文翻译:

通过易于获得的α-炔基烯甲酰胺的解构性卤化羰基化连接甲酰胺束缚的α-卤代炔酮

在本文中,我们描述了一种化学选择性,区域选择性,模块化和高效解构的氧代卤代化策略,该策略通过骨架将易得的环状α-炔基烯甲酰胺重塑为甲酰胺束缚的α-卤代炔酮。这种脚手架的转换提供了多种架构,而这些架构将很难通过传统的断开连接来实现。

更新日期:2020-03-12
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