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- W2070946912 abstract "In this Communication, we report a system in which an achiral Lewis acid (activating the diene) works in concert with a chiral nucleophile (dienophile) to effect the first highly enantio- and regioselective catalytic inverse electron demand Diels−Alder [4 + 2] cycloaddition reaction to form biologically active quinoxalinones from ketene enolates and o-benzoquinone diimides in good to excellent yields with >99% ee." @default.
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- W2070946912 date "2006-09-21" @default.
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- W2070946912 title "Catalytic, Enantioselective Bifunctional Inverse Electron Demand Hetero-Diels−Alder Reactions of Ketene Enolates and <i>o</i>-Benzoquinone Diimides" @default.
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- W2070946912 doi "https://doi.org/10.1021/ja065754d" @default.
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