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- W2801863457 abstract "Reported herein is a general approach to optically active isoflavanes based on a chiral amine-catalyzed [4 + 2] asymmetric annulation of o-quinone methides and aldehydes. A number of naturally occurring isoflavanes, including equol, sativan, isosativan, vestitol and medicarpin, as well as isoflavane analogues were readily prepared with good to excellent enantioselectivities." @default.
- W2801863457 created "2018-05-17" @default.
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- W2801863457 date "2018-06-01" @default.
- W2801863457 modified "2023-10-16" @default.
- W2801863457 title "A general asymmetric route to enantio-enriched isoflavanes via an organocatalytic annulation of o-quinone methides and aldehydes" @default.
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- W2801863457 doi "https://doi.org/10.1016/j.tetlet.2018.05.016" @default.
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