Bulletin of the Chemical Society of Japan p. 1355 - 1362 (1986)
Update date:2022-07-29
Topics: Intramolecular Diels-Alder Reaction Fused
Noguchi, Michihiko
Kakimoto, Shinji
Kawakami, Hisao
Kajigaeshi, Shoji
The 2-pyrone-6-carboxamides, prepared from 2-pyrone-6-carbonyl chloride and substituted allylamine, undergo intramolecular Diels-Alder reaction spontaneously to give 3a,4,5,7a-tetrahydro-1-oxoisoindoline-5,7a-carbolactones, which regenerate the diene moie
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Doi:10.1007/BF01175056
(1986)Doi:10.1021/ja025608h
(2002)Doi:10.1007/BF01175059
(1986)Doi:10.1016/j.tetlet.2008.09.008
(2008)Doi:10.1021/jo01351a055
(1961)Doi:10.1016/j.tet.2019.02.038
(2019)
