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- W2084797287 abstract "The diastereoseiective reduction of a range of acyclic β-hydroxy ketones with triacetoxyborohydride is described. In all cases, the anti 1,3-diol diastereomer is the principal product (eq 1). The selective reduction of a range of 3-hydroxy ketones with triacetoxyborohydride is described. In all cases the principal product is the anti 1,3-diol. Mechanistic observations support the contention that the reduction is directed via the hydroxyl group." @default.
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- W2084797287 date "1986-01-01" @default.
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- W2084797287 title "The directed reduction of β-hydroxy ketones employing Me4NHB(OAc)3" @default.
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- W2084797287 doi "https://doi.org/10.1016/s0040-4039(00)85367-8" @default.
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