An article Sterically hindered N-heterocyclic carbene/palladium(ii) catalyzed Suzuki-Miyaura coupling of nitrobenzenes WOS:000478612600005 published article about PALLADIUM; COMPLEXES; NICKEL; NITROARENES; CONVERSION; CARBENES; ELECTROPHILES; AMINATION; CALCIUM; ESTERS in [Chen, Kai; Chen, Wei; Yi, Xiaofei; Chen, Wanzhi] Zhejiang Univ, Dept Chem, 38 Zheda Rd, Hangzhou 310027, Zhejiang, Peoples R China; [Liu, Miaochang; Wu, Huayue] Wenzhou Univ, Coll Chem & Mat Engn, Wenzhou 325027, Peoples R China in 2019.0, Cited 46.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Quality Control of 1-(4-Nitrophenyl)ethanone
Palladium-catalyzed denitrative Suzuki coupling of nitroarenes using 2-aryl-5-(2,4,6-triisopropylphenyl)-2,3-imidazolylidene[1,5-a]pyridines as the ligands is described. The key to success is the use of the NHC ligands which show strong donating ability and suitable steric hindrance allowing the successful oxidative addition of Ar-NO2 bonds. Both aromatic and aliphatic boronic acids are tolerated, and a variety of biphenyls and alkylarenes were obtained in good to excellent yields.
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Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem