Abstract
We describe a palladium-catalyzed deoxygenative transfer hydrogenation of ketones using B2(OH)4 as the sole additive. Deuterium labeling experiments using B2(OD)4 show that the incorporated protons originate exclusively from the diboron reagent. Spectroscopic evidence implicates the intermediacy of a borate ester. A wide array of aromatic ketones can be deoxygenated using this approach.
Supplementary materials
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Supporting Information
Description
Supporting information for Tetrahydroxydiboron-Mediated Palladium-Catalyzed Deoxygenative Transfer Hydrogenation of Aryl Ketones
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