4.8 Article

Asymmetric Dearomative Cascade Multiple Functionalizations of Activated N-Alkylpyridinium and N-Alkylquinolinium Salts

Journal

ORGANIC LETTERS
Volume 22, Issue 19, Pages 7617-7621

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.0c02828

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Funding

  1. National Natural Science Foundation of China [21772126, 21961132004, 21931006]

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An enantioselective cascade reaction of N-alkylpyridinium and -quinolinium salts with o-hydroxybenzylideneacetones to access fused polyheterocycles through cross dienamine-mediated addition followed by trapping of the dearomatized enamine-type intermediates and aminal formation has been developed. A cascade assembly of N-benzyl-4-methylpyridinium salt and cyclic 2,4-dienones is further disclosed to give bridged frameworks via repetitive dearomatization and aromatization activation.

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