313967-69-0Relevant articles and documents
Steric and electronic substitution effects on the thermal oxidation of 5-carboethoxy-2-oxo-1,2,3,4-tetrahydropyridines
Memarian, Hamid Reza,Kalantari, Mahdieh
, p. 143 - 155 (2017/01/05)
Various 4-aryl substituted 5-carboethoxy-2-oxo-1,2,3,4-tetrahydropyridines were oxidized to their corresponding 4-aryl-5-carboethoxy-2-oxo-1,2-dihydropyridines by potassium peroxydisulfate in aqueous acetonitrile under thermal conditions. The products wer
High-throughput preparation of alkyl 4-aryl substituted-2-methyl-6-thioxo- 1,4,5,6-tetrahydropyridine-3-carboxylates under microwave irradiation
Rodriguez, Hortensia,Coro, Julieta,Lam, Anabel,Salfran, Esperanza,Rodriguez-Salarichs, Javier,Suarez, Margarita,Albericio, Fernando,Martin, Nazario
experimental part, p. 125 - 141 (2011/08/07)
An efficient high-throughput synthesis of 4-aryl substituted 1,4,5,6-tetrahydro-2-methyl-6-thioxopyridine-3-carboxylates 5a-p was developed by using Lawesson's reagent, a very effective thionating reagent for carbonyl compounds, under conventional conditi
Simple and efficient one-pot synthesis of 3,4-dihydro-2-pyridones via solid-supported Bi(III)nitrate catalyzed double Michael addition-azaannulation
Singh, Jagjeet,Koui, Summon,Pannu, Ajay P. S.,Sharma, Rattan L.,Razdan, Tej K.
, p. 349 - 357 (2008/09/20)
(Chemical Equation Presented) 4-Aryl-5-carboethoxy-6-methyl-2,3-dihydro-2- pyridones were obtained, in high yield, by heating ternary mixtures of appropriate aldehydes, ethylacetoacetate and compounds possessing NH 2-C=X functionality, in prese