Authors Khakyzadeh, V; Rostami, A; Veisi, H; Shaghasemi, BS; Reimhult, E; Luque, R; Xia, YZ; Darvishi, S in ROYAL SOC CHEMISTRY published article about ONE-POT SYNTHESIS; MICHAEL-CYCLOCONDENSATION REACTION; ARYL BORONIC ACIDS; COUPLING REACTIONS; LIGAND-FREE; H BOND; TRIPHENYLTIN CHLORIDE; EFFICIENT CATALYST; ODORLESS SYNTHESIS; ARYLBORONIC ACIDS in [Khakyzadeh, Vahid; Darvishi, Sima] KN Toosi Univ Technol, Dept Chem, POB 16315-1618, Tehran 15418, Iran; [Rostami, Abed] Kurdistan Univ Med Sci, Food & Drug, Sanandaj, Iran; [Veisi, Hojat] Payame Noor Univ, Dept Chem, Tehran, Iran; [Shaghasemi, Behzad Shirmardi; Reimhult, Erik] Univ Nat Resources & Life Sci, Dept Nanobiotechnol, Inst Biol Inspired Mat, Muthgasse 11, A-1190 Vienna, Austria; [Luque, Rafael] Univ Cordoba, Dept Quim Organ, Edif Marie Curie,Ctra Nnal 4-A,Km 396, E-14014 Cordoba, Spain; [Luque, Rafael] Peoples Friendship Univ Russia, RUDN Univ, 6 Miklukho Maklaya Str, Moscow 117198, Russia; [Xia, Yuanzhi] Wenzhou Univ, Coll Chem & Mat Engn, Wenzhou 325035, Peoples R China in 2019.0, Cited 76.0. Application In Synthesis of 4′-Hydroxyacetophenone. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4
A dual-metal catalysis system including a newly prepared nanoparticle [SiO2@ organic-linker(OL)@ Pd(II)] and CuI was introduced with ultra-high catalytic activity (high turnover number (TON), up to 19 000) to a one-pot and odorless synthesis of unsymmetrical aryl sulfides by crossover C-S bond formation. The reaction proceeds via C-O bond activation of phenols and direct C-S bond formation in the presence of S8 as an oddorless sulfur source and aryl boronic acids under mild conditions (room temperature). The catalyst could be recycled up to five times without an obvious change in its activity.
Application In Synthesis of 4′-Hydroxyacetophenone. About 4′-Hydroxyacetophenone, If you have any questions, you can contact Khakyzadeh, V; Rostami, A; Veisi, H; Shaghasemi, BS; Reimhult, E; Luque, R; Xia, YZ; Darvishi, S or concate me.
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles