Regioselective formation of 4-isoxazolines from n-aryl nitrones and alkynes

DOI: 10.1016/S0040-4020(01)85905-6

Source and publish data:

Tetrahedron p. 1247 - 1253 (1988)

Update date:2022-08-05

Topics:

Authors:

Libuori Libuori

Ottana Ottana

Romeo Romeo

Sindona Sindona

Uccella Uccella

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Article abstract of DOI:10.1016/S0040-4020(01)85905-6

4-Regioisomeric 4-isoxazolines are selectively formed by 1,3-dipolar cycloaddition of N-arylnitrones to substituted alkynes. The reactivity and regioselectivity of the addition process are interpreted by the application of FMO principles. Secondary orbita

Full text of DOI:10.1016/S0040-4020(01)85905-6

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