The author of 《Palladium Catalyzed Regioselective C4-Arylation and Olefination of Indoles and Azaindoles》 were Thrimurtulu, Neetipalli; Dey, Arnab; Singh, Anurag; Pal, Kuntal; Maiti, Debabrata; Volla, Chandra M. R.. And the article was published in Advanced Synthesis & Catalysis in 2019. Formula: C7H7I The author mentioned the following in the article:
A convergent strategy for the synthesis of biol. relevant C4-substituted indole scaffolds was demonstrated using Pd(II)-catalyzed remote C-H functionalization of indoles and azaindoles. The reaction displayed high regioselectivity for the C4-position of indole-3-carbaldehydes using glycine as an inexpensive transient directing group. Notable features of this transformation included the selective formation of six-membered palladacyle and excellent functional group tolerance. The experimental part of the paper was very detailed, including the reaction process of 1-Iodo-4-methylbenzene(cas: 624-31-7Formula: C7H7I)
1-Iodo-4-methylbenzene(cas: 624-31-7) undergoes Suzuki-Miyaura coupling reaction with phenylboronic acid catalyzed by (Ni,Mg)3Si2O5(OH)4 solid-solution nanotubes loaded with palladium.Formula: C7H7I
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com