Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Aydeé Fuentes‐Benítes"'
Autor:
Carlos A. González-González, Juan Javier Mejía Vega, Ricardo García Monroy, Davir González-Calderón, David Corona-Becerril, Aydeé Fuentes-Benítes, Joaquín Tamariz Mascarúa, Carlos González-Romero
Publikováno v:
Journal of Chemistry, Vol 2017 (2017)
The process of N-alkylation of several pyrroles, indoles, and derivative heterocycles is herein described, using quaternary ammonium salts as the source of an alkylating agent. These reactions were carried out on several heterocyclic rings with triet
Externí odkaz:
https://doaj.org/article/5a87c165f2614da5a744ea10f8907174
Autor:
Juana Suárez-García, Ma-Angeles Cano-Herrera, Alejandra Ramírez-Villalva, M. V. Basavanag Unnamatla, Aydeé Fuentes-Benítes, Erick Cuevas-Yañez, Marco A. García-Eleno, Nieves Zavala-Segovia
Publikováno v:
Pharmaceutical Chemistry Journal. 55:436-440
Aseries of 1-(2-aryloxy-2-phenylethyl)-1,2,3-triazole derivatives (Miconazole analogs) was obtained via copper catalyzed azide-alkyne cycloaddition as the key step. The synthesized compounds were evaluated for antimicrobial activity against Candida g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a500ac5a83da4aff79b1371fc7144437
https://doi.org/10.1007/s11094-021-02440-x
https://doi.org/10.1007/s11094-021-02440-x
Autor:
Salvador Mastachi‐Loza, Tania I. Ramírez‐Candelero, Luis J. Benítez‐Puebla, Aydeé Fuentes‐Benítes, Carlos González‐Romero, Miguel A. Vázquez
Publikováno v:
Chemistry – An Asian Journal. 17
Chalcones are aromatic ketones found in nature as the central core of many biological compounds. They have a wide range of biological activity and are biogenetic precursors of other important molecules such as flavonoids. Their pharmacological releva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f759960f34edaecc8bdcb5587380f9c
https://doi.org/10.1002/asia.202200706
https://doi.org/10.1002/asia.202200706
Autor:
Edson Barrera, R. Israel Hernández‐Benitez, Carlos A. González‐González, Carlos H. Escalante, Aydeé Fuentes‐Benítes, Carlos González‐Romero, Elvia Becerra‐Martínez, Francisco Delgado, Joaquín Tamariz
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a9fb55861c1814d7c4a43e8efeed2e7
https://doi.org/10.1002/ejoc.202200364
https://doi.org/10.1002/ejoc.202200364
Autor:
Eva Ramón-Gallegos, Miguel A. Vázquez, Aarón Mendieta, María del Carmen Cruz-López, Catalina Rugerio-Escalona, Abraham Pucheta, Germán Chamorro-Cevallos, Alejandra Ramírez-Villalva, Francisco Delgado, Joaquín Tamariz, Liseth Romero, Fabiola Jiménez, Damian A. Madrigal, Carlos González-Romero, Alfonso Sequeda-Juárez, Omar Gómez-García, Leticia Garduño-Siciliano, Roberto I. Hernández-Benitez, Aydeé Fuentes-Benítes, Lourdes Villa-Tanaca, Blanca Rosales-Acosta, Julio López
Publikováno v:
Medicinal Chemistry Research. 29:459-478
A series of highly potent antihyperlipidemic agents constituted by a fibrate-based structure was recently reported by our group, whose synthesis started from isovanillin derivatives. In the interest of evaluating the bioisosteric effect of the vanill
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76107399cbe7003911c6565497181e3f
https://doi.org/10.1007/s00044-019-02496-1
https://doi.org/10.1007/s00044-019-02496-1
Autor:
Josué Varela-Palma, Alejandra Ramírez-Villalva, Marco A. García-Eleno, Erick Cuevas-Yañez, M. V. Basavanag Unnamatla, Aydeé Fuentes-Benítes, Omar Valdez-Arcos
Publikováno v:
Pharmaceutical Chemistry Journal.
A small series of 4′-substituted 1,3-bis-1,2,3-triazol-1-yl-propan-2-ol compounds was prepared via CuAAC click reaction of 1,3-diazido-2-propanol and various alkynes R. Antifungal evaluation of these molecules revealed important activity against so
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::730c9678a398f84198f5946a054d928d
https://doi.org/10.1007/s11094-021-02428-7
https://doi.org/10.1007/s11094-021-02428-7
Autor:
Joaquín Tamariz, Aydeé Fuentes-Benítes, Salvador Mastachi-Loza, Eduardo Díaz-Torres, Asenet Tapia-Bustamante, Rubén A. Toscano, Tania I. Ramírez-Candelero, Carlos González-Romero
Publikováno v:
Tetrahedron Letters. 60:1370-1374
The synthesis of novel of 4,5,6,7-tetrahydrobenzoxazol-2-ones is herein reported. They were obtained in moderate to good yields by a highly regio- and stereoselective Diels-Alder cycloaddition of N-substituted exo-oxazolidin-2-one dienes with chalcon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b118b0835732cc6e5d1f5497d30e4bf
https://doi.org/10.1016/j.tetlet.2019.04.027
https://doi.org/10.1016/j.tetlet.2019.04.027
Autor:
C. K. Jankowski, Joaquín Barroso-Flores, Janneth Cruz-de la Cruz, Ezequiel Silva-Nigenda, E. Diaz-Torres, Erick Cuevas-Yañez, Alejandro Martínez-Gómez, Carlos González-Romero, Aydeé Fuentes-Benítes, David Corona-Becerril
Publikováno v:
Journal of Molecular Structure. 1176:562-566
Long range 5J and 6J (1H 19F) spin-spin coupling constants for a set of nine biarylic fluorinated derivatives were determined by 1H NMR experiments. The quantitation of these long-range 5J and 6J (1H 19F) coupling can be found through the measure of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19174051238fb0cdc941d2399c862761
https://doi.org/10.1016/j.molstruc.2018.08.084
https://doi.org/10.1016/j.molstruc.2018.08.084
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40cb5c6c1572db448c85804040fd0acb
https://doi.org/10.29356/jmcs.v65i2.1457
https://doi.org/10.29356/jmcs.v65i2.1457
