
Journal of Organic Chemistry p. 5570 - 5574 (1987)
Update date:2022-08-11
Topics:
Perez, Daniel
Greenspoon, Noam
Keinan, Ehud
Reductive dehalogenation of α-halo ketones and esters is effectively achieved by using a novel reducing system comprised of phenylsilane and catalytic amounts of molybdenum hexacarbonyl and triphenylphosphine.Reactions are carried out at 60-80 deg C in variety of solvents, including THF, benzene, toluene, and diglyme.With respect to α-halo carbonyl reduction, this combination of Mo(0) and phenylsilane is superior to our previously described palladium (0)/diphenylsilane system and produces higher yields and cleaner products.
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