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Issue 28, 2005
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[5C + 1N] Annulation: a novel synthetic strategy for functionalized 2,3-dihydro-4-pyridones

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Abstract

A novel and facile route to functionalized mono/bicyclic 2,3-dihydro-4-pyridones has been developed via formal [5C + 1N] annulation of readily available α-alkenoyl ketene-(S,S)-acetals with various aliphatic primary amines.

Graphical abstract: [5C + 1N] Annulation: a novel synthetic strategy for functionalized 2,3-dihydro-4-pyridones

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Publication details

The article was received on 21 Apr 2005, accepted on 25 May 2005 and first published on 15 Jun 2005


Article type: Communication
DOI: 10.1039/B505569E
Citation: Chem. Commun., 2005,0, 3580-3582
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    [5C + 1N] Annulation: a novel synthetic strategy for functionalized 2,3-dihydro-4-pyridones

    D. Dong, X. Bi, Q. Liu and F. Cong, Chem. Commun., 2005, 0, 3580
    DOI: 10.1039/B505569E

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