An article Electrochemically initiated intermolecular C-N formation/cyclization of ketones with 2-aminopyridines: an efficient method for the synthesis of imidazo[1,2-a]pyridines WOS:000464318800007 published article about ONE-POT SYNTHESIS; H FUNCTIONALIZATION; ORGANIC ELECTROSYNTHESIS; ANTITUMOR EVALUATION; OXIDATIVE AMINATION; ANTIVIRAL ACTIVITY; COUPLING REACTION; METAL; DERIVATIVES; INHIBITORS in [Feng, Mei-Lin; Li, Shu-Qi; He, Hui-Zi; Xi, Long-Yi; Chen, Shan-Yong; Yu, Xiao-Qi] Sichuan Univ, Dept Coll Chem, Minist Educ, Key Lab Green Chem & Technol, Chengdu 610064, Sichuan, Peoples R China in 2019.0, Cited 106.0. Category: benzodioxans. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6
Electrochemical intermolecular C-N formation/cyclization of ketones with 2-aminopyridines using catalytic hydriodic acid as the redox mediator was developed, providing imidazo[1,2-a]pyridines under more environmentally benign conditions. The reaction proceeds in a simple undivided cell, using low toxic ethanol as the solvent, without external oxidants, and exhibits high atom economy. A variety of ketones including acetophenones, unsatruated and alkyl ketones are amenable to this reaction, affording the corresponding products in moderate to excellent yields. A three-component tandem reaction realizing C-N, C-S/C-Se bond formation can also be achieved under standard conditions.
Welcome to talk about 100-19-6, If you have any questions, you can contact Feng, ML; Li, SQ; He, HZ; Xi, LY; Chen, SY; Yu, XQ or send Email.. Category: benzodioxans
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Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem