Anodic oxidation of 2,3-diarylbenzofurans : Different reaction pathways for the cation radical

DOI: 10.1016/S0040-4039(00)93495-6

Source and publish data:

Tetrahedron Letters p. 4913 - 4916 (1991)

Update date:2022-08-03

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Authors:

Cariou, Michel

Simonet, Jacques

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Article abstract of DOI:10.1016/S0040-4039(00)93495-6

The electrooxidation of 2,3-diarylbenzofurans leads to a rearrangement lactone, 3,3-diaryl-2(3H)-benzofuranone, together with a ring enlargement product, 9-aroyl-9-hydroxy-(9H)-xanthene. However, in some cases coupling products may be isolated in high yie

Full text of DOI:10.1016/S0040-4039(00)93495-6

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