Authors Martelli, LSR; Vieira, LCC; Paixao, MW; Zukerman-Schpector, J; de Souza, JO; Aguiar, ACC; Oliva, G; Guido, RVC; Correa, AG in PERGAMON-ELSEVIER SCIENCE LTD published article about ALPHA,BETA-UNSATURATED GAMMA-BUTYROLACTAM; ENANTIOSELECTIVE SYNTHESIS; ADDITION-REACTIONS; CONSTRUCTION; BUTENOLIDES in [Martelli, Lorena S. R.; Vieira, Lucas C. C.; Paixao, Marcio W.; Zukerman-Schpector, Julio; Correa, Arlene G.] Univ Fed Sao Carlos, Ctr Excellence Res Sustainable Chem, Dept Chem, BR-13565905 Sao Carlos, SP, Brazil; [Vieira, Lucas C. C.] Univ Fed Mato Grosso, Inst Engn, BR-78060900 Cuiaba, MT, Brazil; [de Souza, Juliana O.; Aguiar, Anna Caroline C.; Oliva, Glaucius; Guido, Rafael V. C.] Univ Sao Paulo, Ctr Innovat Biodivers & Drug Discovery, Sao Carlos Inst Phys, BR-13563120 Sao Carlos, SP, Brazil in 2019.0, Cited 44.0. Safety of 1-(4-Nitrophenyl)ethanone. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6
The organocatalysed asymmetric vinylogous Michael addition of alpha,alpha-dicyanoolefins to alpha,beta-unsaturated aldehydes and ketones have been reported in the last decade, however, chalcones have been poorly explored. Moreover, a considerable part of the publications in this theme still employs undesirable solvents, such as toluene and THF, with concerns related to health and environmental safety. We report herein the use of a bifunctional catalyst derived from a Cinchona alkaloid to perform the enantio- and diastereoselective Michael addition of alpha,alpha-dicyanoolefins to chalcones using 2-MeTHF as solvent. The Michael adducts were obtained in moderate to good yields and were evaluated for their antiplasmodial and cytotoxic activity. (C) 2019 Elsevier Ltd. All rights reserved.
Safety of 1-(4-Nitrophenyl)ethanone. Welcome to talk about 100-19-6, If you have any questions, you can contact Martelli, LSR; Vieira, LCC; Paixao, MW; Zukerman-Schpector, J; de Souza, JO; Aguiar, ACC; Oliva, G; Guido, RVC; Correa, AG or send Email.
Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem