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a transforma-tion of the MBH acetates, obtained from 2-halobenzaldehydeor 2-chloroquinoline-3-carboxaldehyde with 2-cyclohexen-1-one, with a base into 2-arylmethylphenol or 2-(quinoline-3-yl)methylphenol, respectively. This reaction proceeded bya base assisted elimination of acetic acid and following keto–enol tautomerization and aromatization by 1,5-hydrogentransfer. Although the acetylated MBH adduct between 2-cyclohexen-1-one and 2-chloropyridine-3-carboxaldehyde or2-chloroquinoline-3-carboxaldehyde are known,

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Morita.Baylis.Hillman Route to 8,9,9a,10-Tetrahydrobenzo[b][1,8]naphthyridine-6(7H)-ones and 3,4,4a,5-Tetrahydrodibenzo[b,g][1,8]naphthyridine-1(2H)-ones