Intramolecular cyclizations of N-acyliminium ions with pyridine rings

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Abstract

The reaction of N-acyliminium ions with several activated pyridines resulted in an intramolecular cyclization to provide novel heterocycles. The reaction exhibited a regiochemical preference for cyclization para to the electron donating substitutent.

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Padwa, A., & Brodney, M. A. (2002). Intramolecular cyclizations of N-acyliminium ions with pyridine rings. Arkivoc, 2002(6), 35–48. https://doi.org/10.3998/ark.5550190.0003.605

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