REARRANGEMENTS OF REGIOISOMERIC 4-ISOXAZOLINES: THE NOVEL FORMATION OF ENAMINODERIVATIVES

DOI: 10.1016/S0040-4020(01)85906-8

Source and publish data:

Tetrahedron p. 1255 - 1266 (1988)

Update date:2022-09-26

Topics: Rearrangement Formation Regioisomeric

Authors:

Liguori, A.

Ottana, R.

Romeo, G.

Sindona, G.

Uccella, N.

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Article abstract of DOI:10.1016/S0040-4020(01)85906-8

Regioisomeric 4-isoxazolines are formed by 1,3-dipolar cycloaddition of C-benzoyl-N-phenylnitrone to electron-deficient alkynes.The 4- and 5-substituted cycloadducts react in different modes under the same conditions yielding enaminoderivatives, via a nov

Full text of DOI:10.1016/S0040-4020(01)85906-8

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