Decay of electrogenerated dianions of acidic indenes: an ‘indirect’ self-protonation mechanism
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1991/P2/P29910001249
Reference25 articles.
1. Kinetics and mechanism of self-protonation reactions in organic electrochemical processes
2. Electrochemical reduction of activated carbon-carbon double bonds. 1. Mechanism and stereochemistry of the reduction of phenyl-substituted indenes
3. Electrochemical reduction of activated carbon–carbon double bonds. Part 2. Mechanism and stereochemistry of the reduction of self-protonating indenes
4. Electrohydrodimerization Reactions: VI . Rotating‐Ring Disk Electrode and Macroscale Electrolysis Studies of the Second Reduction Wave of Diethyl Fumarate
5. An “indirect” self-protonation process in the electrochemical reduction of phenyl-substituted indenes
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3. Electrochemical reduction of phenyl-substituted cyclopentadienes: a case of an ‘indirect father–son’ self-protonation process;Journal of Electroanalytical Chemistry;1999-01
4. A case of the indirect role of traces of water in the electroreduction of organic substrates;Journal of Electroanalytical Chemistry;1996-11
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