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-Reference-Cited by-同舟云学术

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

Published:1992-07 Issue:1-2 Volume:328 Page:63-73
ISSN:1572-6657
Container-title:Journal of Electroanalytical Chemistry
language:en
Short-container-title:Journal of Electroanalytical Chemistry

Author:

Vincent Matthew L.,Peters Dennis G.

Publisher

Elsevier BV

Subject

Electrochemistry,General Chemical Engineering,Analytical Chemistry

Reference22 articles.

1. Reduction of aromatic hydrocarbons. I. Polarographic and electron spin resonance studies of 4,5-methylenephenanthrene

2. Mechanism and stereochemistry of the electrochemical reduction of substituted indenes

3. Electrochemical reduction of activated carbon-carbon double bonds. 1. Mechanism and stereochemistry of the reduction of phenyl-substituted indenes

4. An “indirect” self-protonation process in the electrochemical reduction of phenyl-substituted indenes

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2. Electrochemical reduction of phenyl-substituted cyclopentadienes: a case of an ‘indirect father–son’ self-protonation process;Journal of Electroanalytical Chemistry;1999-01

3. A case of the indirect role of traces of water in the electroreduction of organic substrates;Journal of Electroanalytical Chemistry;1996-11

4. Reductive elimination in vicinal dibromides. Electrochemical reduction of 1,2-dibromo-3-(4-substituted)-phenylpropanes and induction of double-bond migration in the resulting olefins.;Journal of Electroanalytical Chemistry;1994-06