Copper(I) Bromide Catalyzed Arylation of Cyclic Enamides and Naphthyl-1-acetamides Using Diaryliodonium Salts was written by Prakash, Muthuraj;Muthusamy, Subramaniam;Kesavan, Venkitasamy. And the article was included in Journal of Organic Chemistry in 2014.Related Products of 1204518-02-4 The following contents are mentioned in the article:
Copper(I) bromide catalyzed direct C-H arylation of cyclic enamides was achieved using diaryliodonium salts in the absence of base/additive at ambient temperature with high yields. E.g., in presence of CuBr in CH2Cl2 at 25 °C, arylation of cyclic enamide (I) with diaryliodonium triflate (II) gave 82% III. A biol. active dihydrobenzo[a]carbazole scaffold was synthesized using the established protocol. The scope of the current methodol. was further extended for the synthesis of C4-, C7-aryl-substituted 1-naphthylacetamides in good yields. This study involved multiple reactions and reactants, such as Mesityl(p-tolyl)iodonium trifluoromethanesulfonate (cas: 1204518-02-4Related Products of 1204518-02-4).
Mesityl(p-tolyl)iodonium trifluoromethanesulfonate (cas: 1204518-02-4) belongs to iodide derivatives. The indole subunit is an almost ubiquitous component of biologically active natural products, and its study has been the focus of research for decades. In addition to indole, the strain-release chemistry worked for numerous substrates including amines, alcohols, thiols, carboxylic acids, imidazoles, and pyrazoles.Related Products of 1204518-02-4
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com