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- W2295324964 endingPage "1293" @default.
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- W2295324964 abstract "Catalyzed by a rhodium complex of P-stereogenic diphosphine ligand (R)-2-tert-butylmethylphosphino-3-(di-tert-butylphosphino)quinoxaline ((R)-3H-QuinoxP*), five-membered cyclic α-dehydroamino ketones bearing endocyclic vinyl and endocyclic keto-carbonyl groups were sequentially hydrogenated to give chiral cyclic trans-β-amino alcohols with two contiguous stereocenters in quantitative conversions, excellent enantioselectivities and good diastereoselectivities." @default.
- W2295324964 created "2016-06-24" @default.
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- W2295324964 date "2016-03-08" @default.
- W2295324964 modified "2023-10-15" @default.
- W2295324964 title "Rh-Catalyzed One-Pot Sequential Asymmetric Hydrogenation of α-Dehydroamino Ketones for the Synthesis of Chiral Cyclic <i>trans</i>-β-Amino Alcohols" @default.
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- W2295324964 doi "https://doi.org/10.1021/acs.orglett.6b00212" @default.
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