Zobrazeno 1 - 9
of 9
pro vyhledávání: '"María Inés Abasolo"'
Autor:
Juan C. Stockert, Juan Manuel Lázaro-Martínez, María C. García Vior, Angeles Villanueva, Albertina G. Moglioni, Maria Mercedes Blanco, María S. Shmidt, Ana Lazaro-Carrillo, Andrea Tabero, Sergio D. Ezquerra Riega, María Inés Abasolo
Publikováno v:
Repositorio Institucional del Instituto Madrileño de Estudios Avanzados en Nanociencia
instname
instname
Quinoline is one of the most important heterocyclic systems in life sciences. Some derivatives are normal metabolites, and others are used as antibacterial, antimalarial, and anticancer agents. In this work, we describe the synthesis, physicochemical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bea416b00a23155871aeb032955d0b4
http://hdl.handle.net/20.500.12614/1826
http://hdl.handle.net/20.500.12614/1826
Autor:
Maria Cristina Caterina, María Inés Abasolo, Maria V. Corona, Carlos de los Santos, Isabel A. Perillo, Alejandra Salerno
Publikováno v:
ARKIVOC, Vol 2014, Iss 4, Pp 228-241 (2014)
Autor:
María Laura Lavaggi, Mercedes González, Hugo Cerecetto, Jonathan Da Cunha, María Inés Abasolo
Publikováno v:
Chemical Biology & Drug Design. 78:960-968
Hypoxic regions of tumours are associated with increased resistance to radiation and chemotherapy. Nevertheless, hypoxia has been used as a tool for specific activation of some antitumour prodrugs, named bioreductive agents. Phenazine dioxides are an
Autor:
Jonathan Da, Cunha, María Laura, Lavaggi, María Inés, Abasolo, Hugo, Cerecetto, Mercedes, González
Publikováno v:
Chemical biologydrug design. 78(6)
Hypoxic regions of tumours are associated with increased resistance to radiation and chemotherapy. Nevertheless, hypoxia has been used as a tool for specific activation of some antitumour prodrugs, named bioreductive agents. Phenazine dioxides are an
Publikováno v:
ChemInform. 24
Publikováno v:
ChemInform. 23
Kinetic studies on the anelation of quinoxalinone derivatives 3a-c and pyrido[2,3-b]pyrazinone derivatives 5a-c and 6a-c synthesized by the Hinsberg reaction is reported. o-Phenylenediamine or 2,3-diaminopyridine were treated with bifunctional carbon
Publikováno v:
Journal of Heterocyclic Chemistry. 29:129-133
Kinetic studies on the anelation of quinoxalinone derivatives 3a-c and pyrido[2,3-b]pyrazinone derivatives 5a-c and 6a-c synthesized by the Hinsberg reaction is reported. o-Phenylenediamine or 2,3-diaminopyridine were treated with bifunctional carbon
Publikováno v:
Journal of Heterocyclic Chemistry. 27:157-162
The regioselective synthesis of pyrido[2,3-b]- and [3,4-b]pyrazine derivatives II by the Hinsberg reaction is reported starting from 2,3 and 3,4-diaminopyridine and excess of pyruvic acid or ethyl pyruvate as reactants. Good yields (higher than 90%)
Publikováno v:
Journal of Heterocyclic Chemistry. 22:577-581
Reaction of some α-phthalimidoacetamides 1a-i with sodium ethoxide was carried out under drastic conditions. Compounds 1b-g afforded 4-hydroxy-1(2H)-isoquinolone-3-carboxamides 2b-g, while 1h-i afforded the acid 3a-b together with the expected isoqu