Zobrazeno 1 - 6
of 6
pro vyhledávání: '"José G. Aguirre-de Paz"'
Autor:
Diana Trujillo-Benítez, Myrna Luna-Gutiérrez, José G. Aguirre-De Paz, Pedro Cruz-Nova, Gerardo Bravo-Villegas, Joel E. Vargas-Ahumada, Paola Vallejo-Armenta, Enrique Morales-Avila, Nallely Jiménez-Mancilla, Rigoberto Oros-Pantoja, Clara Santos-Cuevas, Erika Azorín-Vega, Blanca Ocampo-García, Guillermina Ferro-Flores
Publikováno v:
Pharmaceutics, Vol 16, Iss 4, p 532 (2024)
Recently, we reported a new fibroblast activation protein (FAP) inhibitor radiopharmaceutical based on the 99mTc-((R)-1-((6-hydrazinylnicotinoyl)-D-alanyl) pyrrolidin-2-yl) boronic acid (99mTc-HYNIC-D-Alanine-BoroPro)(99mTc-HYNIC-iFAP) structure for
Externí odkaz:
https://doaj.org/article/0fdb43edc9aa47f6b9827a930acef9fb
Autor:
Salvador Mastachi-Loza, Aydeé Fuentes-Benítes, Davir González-Calderón, José G. Aguirre-de Paz, Alejandra Ramírez-Villalva, Carlos González-Romero, Ricardo García-Monroy
Publikováno v:
Journal of the Mexican Chemical Society. 65
A library of novel benzylic 1,2,3-triazole-4-carboxamides (3a-m) were obtained with acceptable yields via a one-pot procedure. The series of compounds was screened for fungicidal activity and evaluated in vitro against four filamentous fungi and four
Autor:
Davir González-Calderón, José G. Aguirre-de Paz, Carlos González-Romero, Aydeé Fuentes-Benítes
Publikováno v:
Tetrahedron Letters. 59:1760-1762
The exploration of azide-enolate cycloaddition in the synthesis of novel Rufinamide analogs is reported for the first time. A very simple procedure involving the use of β-ketonitriles as dipolarophiles afforded 5-aril/heteroayl Rufinamide derivative
Autor:
Carlos A. González-González, Aydeé Fuentes-Benítes, Davir González-Calderón, José G. Aguirre-de Paz, Carlos González-Romero
Publikováno v:
Tetrahedron Letters. 56:1713-1715
The preparation of 1,4,5-trisubstituted 1,2,3-triazoles by the coupling of three components (alkyl halides, sodium azide, and active ketones) through an azide–enolate [3+2] cycloaddition (Dimroth cycloaddition) has been developed for the first time
Autor:
Carlos A. González-González, Davir González-Calderón, José G. Aguirre-de Paz, Carlos González-Romero, Aydeé Fuentes-Benítes
Publikováno v:
ChemInform. 46
A convenient one-pot procedure for the [3 + 2] cycloaddition reaction of in situ generated organic azides with enolates to produce triazoles in good yields is presented.