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- W2090569439 endingPage "4711" @default.
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- W2090569439 abstract "An electron-withdrawing group was introduced to the α-position of chalcones, and the resulting alkylidene diketones showed new reactivities with enals under the catalysis of N-heterocyclic carbenes (NHCs). Selective activation of enals affords enolate equivalents that undergo highly enantioselective intermolecular Diels-Alder reactions with the alkylidene diketones. No products that might have resulted from typical homoenolate pathways were observed." @default.
- W2090569439 created "2016-06-24" @default.
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- W2090569439 date "2011-08-02" @default.
- W2090569439 modified "2023-09-30" @default.
- W2090569439 title "Enantioselective Diels–Alder Reactions of Enals and Alkylidene Diketones Catalyzed by N-Heterocyclic Carbenes" @default.
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- W2090569439 doi "https://doi.org/10.1021/ol201917u" @default.
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