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• W2953246220 endingPage "4083" @default.
• W2953246220 startingPage "4080" @default.
• W2953246220 abstract "Enantioselective N-heterocyclic carbene-catalyzed Michael addition reactions to α,β-unsaturated aldehydes by redox oxidation were realized. With 10 mol % of camphor-derived triazolium salt D, 15 mol % of DBU, 5 mol % of NaBF(4), and 100 mol % of quinone oxidant, the reactions of various dicarbonyl compounds with α,β-unsaturated aldehydes led to 3,4-dihydro-α-pyrones in good yields and excellent ee's." @default.
• W2953246220 created "2019-06-27" @default.
• W2953246220 creator A5019588728 @default.
• W2953246220 creator A5029205938 @default.
• W2953246220 creator A5040306819 @default.
• W2953246220 date "2011-07-06" @default.
• W2953246220 modified "2023-10-08" @default.
• W2953246220 title "Enantioselective <i>N</i>-Heterocyclic Carbene-Catalyzed Michael Addition to α,β-Unsaturated Aldehydes by Redox Oxidation" @default.
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