An article C-H functionalization of (hetero)arenes: Direct selanylation mediated by Selectfluor WOS:000540277100005 published article about ASSISTED SYNTHESIS; DERIVATIVES; ANTIOXIDANT; EFFICIENT; INDOLES; THIOLATION; SELENATION; SELENIDES; ARENES; CUI in [Belladona, Andrei L.; Cervo, Rodrigo; Cargnelutti, Roberta; Schumacher, Ricardo F.] Fed Univ Santa Maria UFSM, Dept Chem, BR-97105900 Santa Maria, RS, Brazil; [Alves, Diego] Fed Univ Pelotas UFPel, CCQFA, LASOL, POB 354, BR-96010310 Pelotas, RS, Brazil; [Barcellos, Thiago] Univ Caxias UCS, Lab Biotechnol Nat & Synthet Prod, Caxias Do Sul, RS, Brazil in 2020.0, Cited 49.0. The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6. Application In Synthesis of 3,5-Dimethyl-1H-pyrazole
The direct selanylation of a diverse array of (hetero)arenes, including imidazo[2, 1-b]thiazole, imidazo [1, 2-a]pyridine, 1H-indole, 1H-pyrazole, isoxazole and naphthalen-2-ol is presented. The reactions are mediated by Selectfluor, as a stable, easy to handle and commercially available oxidant. The methodology features simple, mild and safe reaction conditions to produce non-symmetrical diorganyl selenides in moderate to excellent yields. The reactions were conducted at room temperature in air using NaHCO3 in acetonitrile. (C) 2020 Elsevier Ltd. All rights reserved.
Welcome to talk about 67-51-6, If you have any questions, you can contact Belladona, AL; Cervo, R; Alves, D; Barcellos, T; Cargnelutti, R; Schumacher, RF or send Email.. Application In Synthesis of 3,5-Dimethyl-1H-pyrazole
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Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics