An “indirect” self-protonation process in the electrochemical reduction of phenyl-substituted indenes
Author:
Publisher
Elsevier BV
Subject
General Medicine,General Chemistry,General Medicine
Reference7 articles.
1. Electrochemical reduction of activated carbon–carbon double bonds. Part 2. Mechanism and stereochemistry of the reduction of self-protonating indenes
2. Kinetics and mechanism of self-protonation reactions in organic electrochemical processes
3. Electrochemical reduction of activated carbon-carbon double bonds. 1. Mechanism and stereochemistry of the reduction of phenyl-substituted indenes
4. The reversible oxidation of aromatic cation radicals to dications. Solvents of low nucleophilicity
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Electrochemical reduction of phenyl-substituted cyclopentadienes: a case of an ‘indirect father–son’ self-protonation process;Journal of Electroanalytical Chemistry;1999-01
2. A case of the indirect role of traces of water in the electroreduction of organic substrates;Journal of Electroanalytical Chemistry;1996-11
3. Computer simulation of large-scale controlled-potential electrolysis. Father—son and grandfather—grandson self-protonation systems;Journal of Electroanalytical Chemistry;1993-01
4. Electrochemically induced isomerization of 1,1,4,4-tetra-phenyl-1,2-butadiene to 1,1,4,4-tetraphenyl-1,3-butadiene: An indirect self-protonation mechanism;Journal of Electroanalytical Chemistry;1992-07
5. Decay of electrogenerated dianions of acidic indenes: an ‘indirect’ self-protonation mechanism;J. Chem. Soc., Perkin Trans. 2;1991
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