Enantioselective: N -heterocyclic carbene-catalyzed nucleophilic dearomatization of alkyl pyridiniums

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Abstract

NHC-catalyzed nucleophilic dearomatization of alkyl pyridiniums has been achieved to generate 1,4-dihydropyridines with high enantioselectivity. This is a rare example of catalytic, asymmetric addition of a nucleophile to the activated pyridinium that prefers C-4 functionalization leading to the 1,4-dihydropyridine with high selectivity.

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Flanigan, D. M., & Rovis, T. (2017). Enantioselective: N -heterocyclic carbene-catalyzed nucleophilic dearomatization of alkyl pyridiniums. Chemical Science, 8(9), 6566–6569. https://doi.org/10.1039/c7sc02648j

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