Enantiomeric excesses of up to 82% are obtained for the α,α-disubstituted products 4 arising from alkylation reactions of borane–amine adducts 2 and 3, which have a chiral nitrogen atom. The structure of diastereomer 2, which can be obtained selectively in the boration of 1, has been established by single-crystal X-ray analysis.
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Ferey et al. (1996) studied this question.
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