Pd-Catalyzed Silicon Hydride Reductions of Aromatic and Aliphatic Nitro Groups
作者:Ronald J. Rahaim、Robert E. Maleczka
DOI:10.1021/ol052120n
日期:2005.10.1
[reaction: see text] Room-temperature reduction of aromaticnitrogroups to amines can be accomplished in high yield, with wide functional group tolerance and short reaction times (30 min) using a combination of palladium(II) acetate, aqueous potassium fluoride, and polymethylhydrosiloxane (PMHS). Replacing PMHS/KF with triethylsilane allows aliphatic nitrogroups to be reduced to their hydroxylamines.
Palladium-Catalyzed Silane/Siloxane Reductions in the One-Pot Conversion of Nitro Compounds into Their Amines, Hydroxylamines, Amides, Sulfonamides, and Carbamates
作者:Robert Maleczka、Ronald Rahaim
DOI:10.1055/s-2006-950231
日期:——
A combination of palladium(II) acetate, aqueous potassi- um fluoride, and polymethylhydrosiloxane (PMHS) facilitates the room-temperature reduction of aromatic nitro compounds to anilines. These reactions tend to be quick (30 min), high-yielding, and tolerate a range of other functional groups. Replacement of PMHS/KF with triethylsilane allows for the reduction of aliphatic nitro compounds to their