Zobrazeno 1 - 10
of 103
pro vyhledávání: '"Martín A. Iglesias-Arteaga"'
Autor:
Pablo Labra-Vázquez, Annia Galano, Margarita Romero-Ávila, Marcos Flores-Álamo, Martín A. Iglesias-Arteaga
Publikováno v:
ARKIVOC, Vol 2013, Iss 4, Pp 107-125 (2013)
Externí odkaz:
https://doaj.org/article/eb42766f87cf4f908addd27985df444b
Autor:
Martín A. Iglesias-Arteaga, Gustavo A. Velázquez-Huerta, José M. Méndez-Stivalet, Annia Galano, J. Raúl Alvarez-Idaboy
Publikováno v:
ARKIVOC, Vol 2005, Iss 6, Pp 109-126 (2005)
Externí odkaz:
https://doaj.org/article/5514e06445d44e32beec6a356fff5da0
Autor:
Omar Viñas-Bravo, Guadalupe Hernández-Linares, Marian Y. Mata-Esma, Roxana Martínez-Pascual, Sara Montiel-Smith, Socorro Meza-Reyes, Sylvain Bernès, Jesús Sandoval-Ramírez, Martín A. Iglesias-Arteaga
Publikováno v:
ARKIVOC, Vol 2003, Iss 11, Pp 163-171 (2003)
Externí odkaz:
https://doaj.org/article/5311a9b2f07142cfa7b84cbd6fa1a038
Autor:
William H. García-Santos, Ariadna M. Quiroz-Mendoza, Martha C. Mayorquín-Torres, MARCOS FLORES-ALAMOS, Martín A. Iglesias-Arteaga
Publikováno v:
Synthesis.
The synthesis of two diastereomeric steroid spiroketals bearing the 2,3-dihydrobenzofuran moiety is described. The structure of the obtained compounds was elucidated by combined 1D and 2d NMR techniques and corroborated by X-ray studies.
Autor:
Gerardo I. Santiago-Sampedro, Andrés Aguilar-Granda, Aaron Torres-Huerta, Marcos Flores-Álamo, Mauricio Maldonado-Domínguez, Braulio Rodríguez-Molina, Martín A. Iglesias-Arteaga
Publikováno v:
The Journal of Organic Chemistry. 87:2255-2266
This work describes the synthesis and aggregation behavior of a dimeric bile acid derivative in which two steroid cores are bridged by a
Autor:
Marcos Flores-Alamo, Martha C. Mayorquín-Torres, Martín A. Iglesias-Arteaga, Mauricio Maldonado-Domínguez
Publikováno v:
Synthesis. 54:643-654
The synthesis of six dimeric spiroketals bearing an estradiol half fused to the 5α- or 5β-epimers of androstane, cholestane, and spirostane nuclei is described. The synthetic procedure comprises the Sonogashira coupling of different steroid alkyn
Publikováno v:
Steroids. 187
The synthesis and characterization of a dimer in which two nuclei of 3β-acetoxy-19-hydroxyandrost-5-en-17-one are linked by the fluorescent 1,4-bis(phenylethynyl)phenylene bridge attached to the oxygenated functions at positions C-19 of each steroid
Autor:
P. Franco Cimino, G. María Núñez, Anielka Rosado-Abón, Ángel Amesty, Ana Estévez-Braun, Katy Díaz, C. Luis Espinoza, Martín A. Iglesias-Arteaga
Publikováno v:
Steroids. :109248
Autor:
Braulio Rodríguez-Molina, Mauricio Maldonado-Domínguez, Marcos Flores-Alamo, Armando Navarro-Huerta, Martha C. Mayorquín-Torres, Martín A. Iglesias-Arteaga
Publikováno v:
The Journal of Organic Chemistry. 86:4112-4120
A series of hybrid dimers having orthogonal steroidal cores bridged by a chroman ketal moiety were obtained by Pd-catalyzed three-component reactions of steroid alkynols, 2-formylestradiol 17-monoacetate, and methyl orthoformate, via ortho-quinone me
Autor:
Marcos Flores-Alamo, Braulio Rodríguez-Molina, Manuel A. Ramos-Enríquez, Martín A. Iglesias-Arteaga, Abraham Colin-Molina
Publikováno v:
Crystal Growth & Design. 20:6649-6659
[23(23E,25R]-23(28)-(3′-Acetoxybenzyliden)-5α-spirostan-3β-ol acetate herein described showed a high tendency to crystallize, growing two solvent-free forms and six solvates that were solved by X-r...