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- W2949711279 abstract "Reductions of cyclic enedione substrates by NaBH4 and by LiAl(O-t-Bu)3H very predominantly gave monoreduction products with very high regio- and stereoselectivity. The reductions involved axial delivery of the hydride. The results indicated that electronic factors were dominated by steric considerations in the transition state of the reduction, even though the seemingly more encumbered carbonyl was reduced." @default.
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- W2949711279 date "1997-05-01" @default.
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- W2949711279 title "Regio- and Stereoselectivity in the Reductions of Cyclic Enedione Systems" @default.
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- W2949711279 doi "https://doi.org/10.1021/jo962377m" @default.
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