68386-85-6Relevant academic research and scientific papers
Facile regiocontrolled three-step synthesis of poly-substituted furans, pyrroles, and thiophenes: Consecutive michael addition of methyl cyanoacetate to α,β-enone, CuI-mediated aerobic oxidation, and acid-catalyzed paal-knorr synthesis
Kim, Se Hee,Lim, Jin Woo,Lim, Cheol Hee,Kim, Jae Nyoung
scheme or table, p. 620 - 624 (2012/05/05)
An efficient synthesis of poly-substituted furans, pyrroles, and thiophenes was carried out in a regiocontrolled manner via a three-step process; (i) conjugate addition of methyl cyanoacetate derivatives to α,β-enones, (ii) CuI-mediated aerobic oxidation,
Reaction of 4-Phenylbut-3-en-2-one with Cyanoacetamide in2:1 Ratio
O'Callaghan, Conor N.,McMurry, T. Brian H.,Cardin, Cristine J.,Wilcock, Deborah J.
, p. 2479 - 2486 (2007/10/02)
The reaction of 4-phenylbut-3-en-2-one with cyanoacetamide is not confined to a 1:1 reaction .The reaction of 2 mole equivalents of 4-phenylbut-3-en-2-one with one of cyanoacetamide
Reactions of α,β-Unsaturated Ketones with Cyanoacetamide
Al-Hajjar, Farouk H.,Jarrar, Adil A.
, p. 1521 - 1525 (2007/10/02)
3-Aryl-1-phenyl-2-propen-1-ones Ia-f and aroylphenylacetylenes Va-d reacted under reflux for 3 hours with cyanoacetamide in the presence of sodium ethoxide to give the corresponding 4-aryl-3-cyano-6-phenyl-2-(1H)pyridones VI.However, when ketones Ia-e wer
