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- W1969808720 abstract "Disubstituted nitroalkenes were converted into enantiomerically enriched amines (isolated as their hydrochloride salts) with enantiomeric excesses of 88 to >95% in three steps: (a) highly stereoselective conjugate addition of the potassium salt of 4-phenyloxazolidin-2-one; (b) radical-mediated removal of the nitro group; (c) cleavage of the oxazolidinone." @default.
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- W1969808720 date "2001-07-01" @default.
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- W1969808720 title "Enantioselective synthesis of α,α-disubstituted amines from nitroalkenes" @default.
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