Journal of the Chemical Society. Perkin transactions I p. 1809 - 1814 (1996)
Update date:2022-08-05
Topics:
Consonni, Roberto
Dalla Croce, Piero
Ferraccioli, Raffaella
La Rosa, Concetta
N-Tosyl- and N-alkylidene-sulfonyl substituted 1,4-dihydro-2A-3,1-benzoxazin-2-ones 2c-g easily undergo thermal carbon dioxide extrusion leading to the aza-ortho-xylylenes 3c-g. The intermediates 3c,d can be trapped by electron-poor ethylenic and acetylenic dienophiles, giving tetrahydroquinoline and quinoline derivatives. The reactions of 2c with non-symmetrical dienophiles are completely regioselective. N-Alkylidenesulfonyl substituted aza-orthro-xylylenes 3f-g undergo intramolecular Diels-Alder reactions leading to the tricyclic compounds 10 and 11, while the aza-ortho-xylylene generated from 4-(hex-5-enyl)-N-(4-methylphenylsulfonyl)-1,4-tetrahydro-2H-3,1-benzoxazin-2-one undergoes a [1,5] hydrogen shift leading to N-[2-(1E)-hepta-1,6-dien-1-ylphenyl]-4-methylbenzenesulfonamide.
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Doi:10.1002/jlac.199619961005
(1996)Doi:10.1021/jo01361a600
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(1996)Doi:10.1016/0040-4039(96)01437-2
(1996)Doi:10.1016/j.tetlet.2004.01.046
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(1996)
