Synchronous concerted bond heterolyses in the solvolysis of substituted benzyl azoxyarenesulphonates and characterization of the transition state
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1989/C3/C39890001358
Cited by 11 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. Nature of solvation effects and mechanism of heterolysis of tert-alkyl halides;Russian Journal of General Chemistry;2007-09
2. Aminolyses of Aryl Diphenylphosphinates and Diphenylphosphinothioates: Effect of Modification of Electrophilic Center from PO to PS;The Journal of Organic Chemistry;2007-04-11
3. Solvolysis of substituted benzyl azoxyarenesulfonates:The IUPAC name for benzyl azoxyarenesulfonate is N-benzyl-N′-arylsulfonyloxydiazene N-oxide. characterisation of the transition state and the selectivity of benzylic intermediates in 50% aqueous 2,2,2-trifluoroethanolElectronic supplementary information (ESI) available: synthesis and analytical data of azoxyarenesulfonates. See http://www.rsc.org/suppdata/p2/b1/b106887n;Journal of the Chemical Society, Perkin Transactions 2;2001-10-17
4. N-Nitroso-N,O-dialkylhydroxylamines: preparation, structure, and mechanism of the hydronium ion catalysed solvolytic nitrous oxide extrusion reaction;Journal of the Chemical Society, Perkin Transactions 2;2000
5. The mechanism of solvolysis of 2-adamantyl azoxytosylate: isotopic labelling, medium effect, and attempted deoxygenation studies;CAN J CHEM;1998
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