Safety of 2,6-Dichlorobenzoic acid. Authors Pacheco-Benichou, A; Ivendengani, E; Kostakis, IK; Besson, T; Fruit, C in MDPI published article about in [Pacheco-Benichou, Alexandra; Ivendengani, Eugenie; Besson, Thierry; Fruit, Corinne] Normandie Univ, UNIROUEN, INSA Rouen, CNRS,COBRA UMR 6014, F-76000 Rouen, France; [Kostakis, Ioannis K.] Natl & Kapodistrian Univ Athens, Dept Pharm, Div Pharmaceut Chem, Athens 15771, Greece in 2021.0, Cited 54.0. The Name is 2,6-Dichlorobenzoic acid. Through research, I have a further understanding and discovery of 50-30-6
Copper-catalyzed Csp2-Csp2 bond forming reactions through C-H activation are still one of the most useful strategies for the diversification of heterocyclic moieties using various coupling partners. A catalytic protocol for the C-H (hetero)arylation of thiazolo[5,4-f]quinazolin-9(8H)-ones and more generally fused-pyrimidinones using catalyst loading of CuI with diaryliodonium triflates as aryl source under microwave irradiation has been disclosed. The selectivity of the transfer of the aryl group was also disclosed in the case of unsymmetrical diaryliodonium salts. Specific phenylation of valuable fused-pyrimidinones including quinazolinone are provided. This strategy enables a rapid access to an array of various (hetero)arylated N-containing polyheteroaromatics as new potential bioactive compounds.
Safety of 2,6-Dichlorobenzoic acid. About 2,6-Dichlorobenzoic acid, If you have any questions, you can contact Pacheco-Benichou, A; Ivendengani, E; Kostakis, IK; Besson, T; Fruit, C or concate me.
Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics