Sonochemical switching from Ionic to Radical Pathways in the Reactions of Styrene and trans-β-Methylstyrene with Lead Tetraacetate

DOI: 10.1016/0040-4039(91)80174-5

Source and publish data:

Tetrahedron Letters p. 6379 - 6382 (1991)

Update date:2022-08-03

Topics:

Authors:

Ando, Takashi

Bauchat, Patrick

Foucaud, Andre

Fujita, Mitsue

Kimura, Takahide

Sohmiya, Hajime

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Article abstract of DOI:10.1016/0040-4039(91)80174-5

The reactions of sryrene and trans-β-methylstyrene with lead tetraacetate in acetic acid are greatly influenced by ultrasonic irradiation to give products resulting mostly from radical chain pathways, whereas mechanical agitation gives products only from ionic processes.

Full text of DOI:10.1016/0040-4039(91)80174-5

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