130747-67-0Relevant academic research and scientific papers
Microwave-Assisted, One-Pot Multicomponent Synthesis of Some New Cyanopyridines
Amer, Amer A.,Abdelhamid, Antar A.
, p. 3126 - 3132 (2017/10/05)
An efficient and facile synthesis of cyanopyridines via a one-pot four-component reaction of aromatic aldehydes, acetophenones, malononitrile, or 2-aminoprop-1-ene-1,1,3-tricarbonitrile in presence of sodium alkoxide or ammonium acetate under both microwave and thermal reaction conditions was introduced.
Synthesis and reactivity of methyl 3-acyl-6-amino-4-aryl-5-cyano-4h-pyran- 2-carboxylates
Sheverdov,Andreev, A. Yu.,Ershov,Nasakin,Tafeenko,Gein
, p. 997 - 1005 (2013/03/13)
By treating arylidenemalononitriles with methyl 2,4-dioxobutanoates, derivatives of 4H-pyrans - methyl 3-acyl-6-amino-4-aryl-5-cyano-4H-pyran-2- carboxylates - are obtained, which are novel, promising structural components for the synthesis of carbo- and
Synthesis of polysubstituted pyridines under combined microwave and ultrasound irradiation: K2CO3-promoted tandem addition/cyclization/hydrogen shift process
Feng, Huangdi,Li, Yuan,Van Der Eycken, Erik V.,Peng, Yanqing,Song, Gonghua
supporting information; experimental part, p. 1160 - 1162 (2012/03/26)
A convenient and efficient K2CO3-promoted tandem reaction of chalcone, malononitrile, and methanol for the synthesis of highly functionalized pyridines has been developed. This multi-component reaction employing the weak nucleophilic agent methanol proceeded smoothly under combined microwave and ultrasound irradiation (CMUI). The reaction mechanism was proposed to consist of a Michael addition, a methoxylation of CN bond, a cyclization to a 1,4-dihydropyridine and an intermolecular hydrogen shift between 1,4-dihydropyridine and initial chalcone.
Reactions of Malononitrile with Acetylenic Esters and Ketones
Kandeel, Kamal A.,Vernon, John M.,Dransfield, Trevor A.,Fouli, Fouli A.,Youssef, Ahmed S. A.
, p. 2101 - 2117 (2007/10/02)
The addition of malononitrile to acetylenic esters and acetylenic ketones catalysed by sodium alkoxides leads to the formation of 3- and 5-cyano-2-pyridones, 2-cyano- and 2,6-dicyano-aniline derivatives, and other products.
