721395-51-3Relevant academic research and scientific papers
Organolead-mediated arylations: 2-(3,3-diphenylallyloxy)phenyllead triacetate as an internal free-radical-trap-containing reagent
Fedorov, Alexey Yu.,Finet, Jean-Pierre
, p. 2040 - 2045 (2004)
2-(3,3-Diphenylprop-2-enyloxy)phenyllead triacetate, an arylating reagent containing an internal free radical trap, was synthesised and its behaviour studied in base-catalysed C-arylation reactions and in copper-catalysed N-arylation reactions. The absence of benzofuran derivatives among the products of C- and N-arylation reactions excludes the involvement of radical species in these two processes. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.
Direct arylation of alkenes with aryl iodides/bromides through an organocatalytic radical process
Sun, Chang-Liang,Gu, Yi-Fan,Wang, Bin,Shi, Zhang-Jie
supporting information; experimental part, p. 10844 - 10847 (2011/10/31)
A radical addition: A KOtBu-complex-promoted radical arylation of polysubstituted alkenes with aryl iodides/bromides proceeds in high efficiency (see scheme). Benzofuran derivatives are also produced starting from readily available allyl 2-iodophenyl ethers. Copyright
