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- W4251273000 endingPage "1831" @default.
- W4251273000 startingPage "1827" @default.
- W4251273000 abstract "Abstract The development of biomimetic chemistry based on the NAD(P)H with hydrogen gas as terminal reductant is a long‐standing challenge. Through rational design of the chiral and regenerable NAD(P)H analogues based on planar‐chiral ferrocene, a biomimetic asymmetric reduction has been realized using bench‐stable Lewis acids as transfer catalysts. A broad set of alkenes and imines could be reduced with up to 98 % yield and 98 % ee , likely enabled by enzyme‐like cooperative bifunctional activation. This reaction represents the first general biomimetic asymmetric reduction (BMAR) process enabled by chiral and regenerable NAD(P)H analogues. This concept demonstrates catalytic utility of a chiral coenzyme NAD(P)H in asymmetric catalysis." @default.
- W4251273000 created "2022-05-12" @default.
- W4251273000 creator A5008944687 @default.
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- W4251273000 creator A5075511300 @default.
- W4251273000 date "2019-01-14" @default.
- W4251273000 modified "2023-10-11" @default.
- W4251273000 title "Catalytic Biomimetic Asymmetric Reduction of Alkenes and Imines Enabled by Chiral and Regenerable NAD(P)H Models" @default.
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- W4251273000 doi "https://doi.org/10.1002/ange.201813400" @default.
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