Electrochemical Reduction of Activated Carbon-Carbon Double Bonds. 1. Mechanism and Stereochemistry of the Reduction of Phenyl-Substituted Indenes

DOI: 10.1021/ja00334a008

Source and publish data:

Journal of the American Chemical Society p. 6503 - 6512 (1984)

Update date:2022-08-02

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Authors:

Farnia, Guiseppe

Marcuzzi, Franco

Melloni, Giovanni

Sandona, Giancarlo

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Article abstract of DOI:10.1021/ja00334a008

The reduction at a Hg electrode in DMF of some phenyl-substituted indenes was carried out, with the aim of finding out possible relationships between stereochemistry and mechanism of the reaction.The two-electron two-proton reduction occured exclusively a

Full text of DOI:10.1021/ja00334a008

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