Electrophilic bromination of aromatic conjugated olefins. II. Mechanism of the dual-path additions in stilbene bromination. Evidence from multiple substituent effects for carbonium ion intermediates
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo00943a019
Cited by 42 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. DCID-mediated Heck cross-coupling of phenols via C–O bond activation;New Journal of Chemistry;2022
2. o-Iodoxybenzoic acid mediated generation of aryl free radicals: synthesis of stilbenes through C–C cross-coupling with β-nitrostyrenes;New Journal of Chemistry;2018
3. Biomimetic Oxidative Dimerization of Anodically Generated Stilbene Radical Cations: Effect of Aromatic Substitution on Product Distribution and Reaction Pathways;The Journal of Organic Chemistry;2014-04-30
4. Cyclic 1,1-bis(silyl)alkenes—new building blocks for the stereoselective synthesis of unsymmetrical (E)-stilbenes and (E,E)-1,4-diarylbuta-1,3-dienes;Tetrahedron;2009-07
5. Kinetic Studies on the Oxidation of Someparaandmeta-Substituted Cinnamic Acids by Pyridinium Bromochromate in the Presence of Oxalic Acid (A Co-oxidation Study);E-Journal of Chemistry;2009
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