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The carbon–carbon double bond of arylidene acetones and chalcones can be selectively reduced with benzeneselenol generated  in situ  by reacting  O -( tert -butyl) Se-phenyl selenocarbonate with hydrochloric acid in ethanol.

rsc advances

Chemoselective and metal-free reduction of α,β-unsaturated ketones by in situ produced benzeneselenol from O-(tert-butyl) Se-phenyl selenocarbonate