Electrochemical Reduction of Activated Carbon-Carbon Double Bonds. Part 2. Mechanism and Stereochemistry of the Reduction of Self-protonating Indenes

DOI: 10.1039/P29880000247

Source and publish data:

Journal of the Chemical Society. Perkin transactions II p. 247 - 254 (1988)

Update date:2022-08-05

Topics: Stereochemistry Mechanism Electrochemical Reduction Activated carbon Carbon-carbon double bonds

Authors:

Farnia, Giuseppe

Sandona, Giancarlo

Marcuzzi, Franco

Melloni, Giovanni

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Article abstract of DOI:10.1039/P29880000247

The reduction at a mercury electrode in dimethylformamide of five variously substituted indenes bearing at least one (acidic) hydrogen at C(1) was carried out, under self-protonation conditions and in the presence of phenol as a proton donor.Reduction occ

Full text of DOI:10.1039/P29880000247

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