Nature of the cationoid intermediates in the solvolytic rearrangement of 2,2-dianisyl-1-arylvinyl bromides in 2,2,2-trifluoroethanol and acetic acid
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo00349a018
Cited by 6 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. Selective esterification of the polyphenol resveratrol at the 4′-position;Tetrahedron Letters;2014-01
2. Photoreactivity of some .alpha.-arylvinyl bromides in acetic acid. Selectivity toward bromide versus acetate ions as a mechanistic probe;Journal of the American Chemical Society;1991-05
3. The rich mechanistic world of nucleophilic vinylic (SN V) substitution;Recueil des Travaux Chimiques des Pays-Bas;1985
4. Vinylic cations from solvolysis. 41. Solvolytic rearrangements of 2,2-dianisyl-1-tolylvinyl bromide and (E)- and (Z)-1,2- dianisyl-2-tolylvinyl bromide;The Journal of Organic Chemistry;1984-11
5. Mass spectrometric analysis of the products from the isotopomeric cationic intermediates in the solvolysis of 1,2-dianisyl-2-p-(2H3)methoxyphenyl[2-13C]vinyl bromide in 70% HOAc – 30% H2O;Canadian Journal of Chemistry;1983-09-01
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