Zobrazeno 1 - 10
of 10
pro vyhledávání: '"María Selma Arias"'
Publikováno v:
e_Buah Biblioteca Digital Universidad de Alcalá
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Here we present a novel family of carbohydrate conjugates based on the 2-aryl-imidazo[4,5-f][1,10]phenanthroline core modified with carbohydrates (carb-APIPs). The hybrid compounds were prepared by direct treatment of the unprotected carbohydrate wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef8abddab1c207e02ac0bf77641611cf
https://doi.org/10.1016/j.bioorg.2022.105851
https://doi.org/10.1016/j.bioorg.2022.105851
Publikováno v:
Bioorganic Chemistry. 81:405-413
A series of novel N1-(4,5-diazafluoren-9-yliden)-N2-glycopyranosyl hydrazines was prepared in synthetically useful yields by treatment of 9H-4,5-diazafluoren-9-hydrazone with different unprotected monosaccharides. The reactions with the monosaccharid
Publikováno v:
Carbohydrate Research. 505:108338
Reductive cleavage of methyl 3,4-O-benzylidene-α-L-fucopyranosides with BH3·THF-TfOH and NaCNBH3-TfOH systems resulted in enhanced reaction rates and selectivity compared to BH3·THF-Bu2BOTf. With this latter system, the nature of the O-2 substitue
Human telomeric G-quadruplex DNA interactions of N-phenanthroline glycosylamine copper(II) complexes
Publikováno v:
Bioorganic & Medicinal Chemistry. 24:33-41
We report in this article the interactions of five N -(1,10-phenanthrolin-5-yl)-β-glycopyranosylamine copper(II) complexes with G-quadruplex DNA. Specifically, the interactions of these compounds with a human telomeric oligonucleotide have been asse
Autor:
María Á. Peña, Nieves Hernández, Antonio Guerrero, María Selma Arias, M.G. Quintanilla, Marta González-Santander, José Luis Copa-Patiño
Publikováno v:
Revista Ibero-Americana de Estudos em Educação, Vol 8, Iss 2, Pp 394-402 (2014)
Revista Ibero-Americana de Estudos em Educação, Vol 8, Iss 2 (2014)
Revista Ibero-Americana de Estudos em Educação, Vol 8, Iss 2 (2014)
En esta comunicación se describe la evolución de una estrategia de innovación educativa, denominada originariamente Semanarios Reflexivos, encaminada a modificar la práctica docente y profundizar en el proceso de enseñanza-aprendizaje en la educ
Autor:
Antonio Peña-Fernández, Mark D. Evans, María Selma Arias, María Á. Peña, G. Quintanilla, Marta González-Santander, José Luis Copa-Patiño, Antonio Guerrero, N. Hernández, M. I. Domínguez
Publikováno v:
Publons
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Knowledge has to be developed firmly based on reflections and thoughts as much as evidence. Being conscious of this principle, our innovation teaching group from the University of Alcalá has developed a reflective pedagogical approach called Guided
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e334f7e3e7ca2b86cfe96d05fc4caf4
http://hdl.handle.net/2086/13969
http://hdl.handle.net/2086/13969
Publikováno v:
J. Chem. Soc., Perkin Trans. 2. :1549-1552
The regioselective protection of secondary hydroxy groups of gluco-, galacto-, manno-, rhamno- and fucopyranosides using TBDPSCl with imidazole in DMF has been studied. It was found that the relative spatial arrangement of the OH groups modulates the
Publikováno v:
e_Buah Biblioteca Digital Universidad de Alcalá
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A series of novel N-(1,10-phenanthrolin-5-yl)-b-glycopyranosylamines was obtained with excellent stereoselectivity and synthetically useful yields by treatment of 5-amino-1,10-phenanthroline with different unprotected monosaccharides, using (NH4)2SO4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22420a9403b361213992348c4d53ce10
https://doi.org/10.1016/j.tet.2013.12.044
https://doi.org/10.1016/j.tet.2013.12.044
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2 (03009580); Apr1991, Issue 4, p467-470, 4p
Publikováno v:
Scopus-Elsevier
Moderately high diastereofacial preference has been observed in the conjugate addition of phenylmagnesium bromide to the acyclic α-enones with an asymmetric carbon at the γ-position (4E,6RS)-2,2,7,7-tetramethyl-6-phenyloct-4-en-3-one (1), (2E,4RS)-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af86ea7a0f893bcd3d1224a6a4dbb039
http://www.scopus.com/inward/record.url?eid=2-s2.0-37049088712&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-37049088712&partnerID=MN8TOARS