SPIRO-ANNULATED CYCLOHEXA-2,5-DIENONES VIA ELECTROOXIDATION OF P-ARYL PHENOLS A NOVEL MODE OF ANODIC CARBON-CARBON BOND FORMATION

DOI: 10.1016/S0040-4039(00)96750-9

Source and publish data:

Tetrahedron Letters p. 5445 - 5448 (1987)

Update date:2022-08-02

Topics:

Authors:

Morrow, Gary W.

Swenton, John S.

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Article abstract of DOI:10.1016/S0040-4039(00)96750-9

Intramolecular trapping of the reactive intermediate from anodic oxidation of 2'-alkenyl substituted p-aryl phenols, followed by solvent capture, affords 4-aryl-4-alkyl-cyclohexa-2,5-dienones.

Full text of DOI:10.1016/S0040-4039(00)96750-9

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