| Literature DB >> 24883040 |
Victor M Tormyshev1, Olga Yu Rogozhnikova2, Michael K Bowman3, Dmitry V Trukhin2, Tatiana I Troitskaya2, Vladimir G Vasiliev2, Leonid A Shundrin2, Howard J Halpern4.
Abstract
C-, N-, P-, and S-nucleophiles reacted with symmetrical tris(2,3,5,6-tetrathiaaryl)methyl cations, generated from the corresponding triarylmethanols by strong acids, to give a variety of asymmetrical monosubstituted persistent triaryl-methyl (TAM) radicals as the major products. The only byproducts were symmetrical TAMs.Entities:
Keywords: Carbocations; Electron transfer; Nucleophilic addition; Radicals; Reaction mechanisms
Year: 2014 PMID: 24883040 PMCID: PMC4038673 DOI: 10.1002/ejoc.201301161
Source DB: PubMed Journal: European J Org Chem ISSN: 1099-0690