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- W2951155087 abstract "Highly enantioselective reduction of 1,2-bis(p-methoxyphenylimino)-1,2-diphenylethane was conducted even with 0.5 mol% of new oxazaborolidine derived form L-threonine and a stoichiometric amount of BH3·THF to give 1,2-diphenylethylenediamine derivative in excellent enantiomeric purity. The subsequent deprotection of nitrogen atoms afforded (R,R)-1,2-diphenylethylenediamine in enantiomerically pure form." @default.
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- W2951155087 date "1995-11-01" @default.
- W2951155087 modified "2023-10-15" @default.
- W2951155087 title "Stereocontrol in the reduction of 1,2-diimine with an oxazaborolidine catalyst. Highly stereoselective preparation of (R,R)-1,2-diphenylethylenediamine" @default.
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- W2951155087 doi "https://doi.org/10.1016/0040-4039(95)01825-3" @default.
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