Radical Additions of Aryl Iodides to Arenes Are Facilitated by Oxidative Rearomatization with Dioxygen

Radical Additions of Aryl Iodides to Are

Radical Additions of Aryl Iodides to Arenes Are Facilitated by Oxidative Rearomatization with Dioxygen.

✍ Dennis P. Curran; Adam I. Keller 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 27 KB

ChemInform Abstract: Syntheses with Perf

ChemInform Abstract: Syntheses with Perfluoroalkyl Radicals from Perfluoroalkyl Iodides. Syntheses with Perfluoroalkyl Iodides. A Review. Part 3. Addition of RFI to Norbornene Esters, Acids and Anhydrides, Alkenoic Acids and Esters, Alkenylsuccinic Anhydrides or Diesters, and to Vinyl Monomers; Lactonization and Other Reactions of Adducts; Hydroperfluoroalkylation by RFI; Synthesis and Reactions of I(CF2)nI Homologues (n = 1—3); Perfluoroalkylation of Arenes by RFI or [RFCO2]2; RF in the Synthesis of RFSR and Segmented RF(CH2)nSH; and, Useful Derivatives Therefrom

✍ Neal O. Brace 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views

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