Rearrangement of Isoxazoline-5-spiro Derivatives. 8. Selective Formation of Tetrahydropyridones from C,C-Disubstituted Nitrones

DOI: 10.1021/jo00047a019

Source and publish data:

Journal of Organic Chemistry p. 5666 - 5670 (1992)

Update date:2022-07-29

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Authors:

Brandi, Alberto

Dueruest, Yasar

Cordero, Franca M.

Sarlo, Francesco De

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Article abstract of DOI:10.1021/jo00047a019

The thermal rearrangement of isoxazolidines 3, 7, 9, 17, and 19 obtained by 1,3-dipolar cycloaddition of C,C-disubstituted nitrones and methylenecyclopropanes 1 and 6 has been studied.The lack of hydrogen at the C-3 position of the isoxazolidine ring lead

Full text of DOI:10.1021/jo00047a019

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