Modular access to formamide-tethered α-halo ynones via the deconstructive oxo-halogenation of readily available α-alkynyl eneformamides
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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.
Beng, T. K., & Farah, A. O. (2020). Modular access to formamide-tethered α-halo ynones via the deconstructive oxo-halogenation of readily available α-alkynyl eneformamides. Tetrahedron Letters, 61(18), 151821. https://doi.org/10.1016/j.tetlet.2020.151821
This article was originally published in Tetrahedron Letters. The full-text article from the publisher can be found here.
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