177763-75-6Relevant academic research and scientific papers
Efficient sonochemical synthesis of alkyl 4-aryl-6-chloro-5-formyl-2- methyl-1,4-dihydropyridine-3-carboxylate derivatives
Ruiz, Enrique,Rodríguez, Hortensia,Coro, Julieta,Niebla, Vladimir,Rodríguez, Alfredo,Martínez-Alvarez, Roberto,De Armas, Hector Novoa,Suárez, Margarita,Martín, Nazario
experimental part, p. 221 - 226 (2012/04/10)
A facile, efficient and environment-friendly protocol for the synthesis of 6-chloro-5-formyl-1,4-dihydropyridine derivatives has been developed by the convenient ultrasound-mediated reaction of 2(1H)pyridone derivatives with the Vilsmeier-Haack reagent. T
USE OF 4, 7-DIHYDROTHIENO [2, 3-B] PYRIDINE COMPOUNDS IN THE TREATMENT OF CARDIOVASCULAR DISEASES
-
Page/Page column 67, (2008/06/13)
This invention relates generally to methods for the treatment of myosin heavy chain (MyHC)-mediated conditions, and in particular, cardiovascular conditions.
A straightforward synthesis and structure of unprecedented iminium salts of dihydropyrido[3,2-e][1,3]thiazines
Suárez, Margarita,Novoa, Hector,Verdecia, Yamila,Ochoa, Estael,Alvarez, Amaury,Pérez, Rolando,Martínez-Alvarez, Roberto,Molero, Dolores,Seoane, Carlos,Blaton, Norbert M.,Peeters, Oswald M.,Martín, Nazario
, p. 1365 - 1371 (2007/10/03)
Unprecedented 2-iminium chloride salts of 5,8-dihydro-2H-pyrido[3,2-e][1,3] thiazines derivatives (8) were easily synthesized in one step from the corresponding o-chloroformyl-1,4-dihydropyridine (2) and thiourea. The structural study has been carried out
Synthesis of methyl 4-aryl-6-methyl-4,7-dihydro-1H-pyrazolo-[3,4-b]pyridine-5-carboxylates from methyl 4-aryl-6-methyl-2-oxo-1,2,3,4-tetrahydropyridine-5-carboxylates
Verdecia, Yamila,Suarez, Margarita,Morales, Alhmed,Rodriguez, Elena,Ochoa, Estael,Gonzalez, Leandro,Martin, Nazario,Quinteiro, Margarita,Seoane, Carlos,Soto, Jose L.
, p. 947 - 951 (2007/10/03)
Novel methyl 4,7-dihydro-1H-pyrazolo[3,4-b]pyridine-5-carboxylates 3a-e have been prepared in a two step procedure from the readily available 2-oxo-1,2,3,4-tetrahydropyridine-5-carboxylates 1a-e by treatment with the Vilsmeier-Haack reagent. Further treat
