Mechanism of benzidine and semidine rearrangements. Part XVIII. Kinetics and products of the acid conversion of 4-acetamidohydrazobenzene, products from 4-aminohydrazobenzene, normality of p-semidine formation, and crossed redox analogues of disproportionation
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/1968/J2/J29680000609
Cited by 7 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. Benzidine rearrangements. 18. Mechanism of the acid-catalyzed disproportionation of 4,4'-diiodohydrazobenzene. Application of heavy-atom kinetic isotope effects;Journal of the American Chemical Society;1983-05
2. Benzidine rearrangement in the presence and absence of micelles. Evidence for rate-limiting proton transfer;Journal of the American Chemical Society;1976-07
3. The Mechanism of the Benzidine Rearrangement. II. The Rearragement of N-Acetylhydrazobenzene;The Journal of Organic Chemistry;1972-07-29
4. Mechanism of benzidine and semidine rearrangements. Part XXV. The acid-catalysed disproportionation of hydrazobenzenes;Journal of the Chemical Society, Perkin Transactions 2;1972
5. Die Disproportionierung von Arylsemicarbaziden;Chemische Berichte;1971-11
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