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Faizi, Darius J; Issaian, Adena; Davis, Ashlee J; Blum, Suzanne A
Journal of the American Chemical Society, 02/2016, Letnik: 138, Številka: 7Journal Article
A catalyst-free oxyboration reaction of alkynes is developed. The resulting borylated isocoumarins and 2-pyrones are isolated as boronic acids, pinacolboronate esters, or potassium organotrifluoroborate salts, providing a variety of bench-stable organoboron building blocks for downstream functionalization. This method has functional group compatibility, is scalable, and proceeds with readily available materials: B-chlorocatecholborane and methyl esters. Mechanistic studies indicate that the B-chlorocatecholborane acts as a carbophilic Lewis acid toward the alkyne, providing a mechanistically distinct pathway for oxyboration that avoids B–O σ bond formation and enables this catalyst-free route.
