Gibbs reaction. Part 1. Reduction of benzoquinone N-chloroimines to benzoquinone imines
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1986/P2/P29860000105
Cited by 4 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. Mechanism of the Gibbs Reaction. Part 4.1 Indophenol Formation via N-Chlorobenzoquinone Imine Radical Anions. The Aza-SRN2 Chain Reaction Mechanism. Chain Initiation with 1,4-Benzoquinones and Cyanide Ion;The Journal of Organic Chemistry;1999-08-11
2. Mechanism of the Gibbs Reaction. 3. Indophenol Formation via Radical Electrophilic Aromatic Substitution (SREAr) on Phenols;The Journal of Organic Chemistry;1994-11
3. The mechanism of the gibbs reaction. Part 2: The ortho ⇉ ortho 2,4-cyclohexadiene-1-one rearrangement of the reaction product of 2,6-di-tert-butyl-4-chlorophenol and 2,6-dichlorobenzoquinone N-chloroimine;Tetrahedron;1994-01
4. ChemInform Abstract: Gibbs Reaction. Part l. Reduction of Benzoquinone N-Chloroimines to Benzoquinone Imines.;Chemischer Informationsdienst;1986-05-13
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