Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Santiago Guisán-Ceinos"'
Autor:
Francisco Rey‐Tarrío, Santiago Guisán‐Ceinos, Juan M. Cuerva, Delia Miguel, Maria Ribagorda, Emilio Quiñoá, Félix Freire
Publikováno v:
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
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Data Availability Statement The data that support the findings of this study are available in the supplementary material of this article.
Acknowledgements We thank Servicio de Microscopía Electrónica (RIAIDT, USC). Financial support from AEI (
Acknowledgements We thank Servicio de Microscopía Electrónica (RIAIDT, USC). Financial support from AEI (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16dd7b12527394d03e4d3398cd34322b
http://hdl.handle.net/10481/76650
http://hdl.handle.net/10481/76650
Autor:
Santiago Guisán-Ceinos, Alexandra R. Rivero, Fernando Romeo-Gella, Silvia Simón-Fuente, Silvia Gómez-Pastor, Natalia Calvo, Alejandro H. Orrego, José Manuel Guisán, Inés Corral, Francisco Sanz-Rodriguez, Maria Ribagorda
Publikováno v:
Biblos-e Archivo. Repositorio Institucional de la UAM
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We present the synthesis, photophysical properties, and biological application of nontoxic 3-azo-conjugated BODIPY dyes as masked fluorescent biosensors of hypoxia-like conditions. The synthetic methodology is based on an operationally simple N=N bon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce1424c580493e730d6b63b292244f11
https://pubmed.ncbi.nlm.nih.gov/35486830
https://pubmed.ncbi.nlm.nih.gov/35486830
Autor:
Pablo Reiné, Juan M. Cuerva, Luis Álvarez de Cienfuegos, Sergio Abbate, Santiago Guisán-Ceinos, Giuseppe Mazzeo, Sandra Resa, María Ribagorda, Giovanna Longhi, Delia Miguel, Antonio J. Mota
Publikováno v:
Organicbiomolecular chemistry. 17(36)
In this work we describe the ability of a simple enantiopure sulfoxide group to promote folding of oligo ortho-phenylene ethynylenes (o-OPEs) with one helical sense. A family of foldamers with up to seven triple bonds was synthesized and fully charac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5aadbe1c0de065e0324c4dbf0092c0c6
https://pubmed.ncbi.nlm.nih.gov/31469142
https://pubmed.ncbi.nlm.nih.gov/31469142
Autor:
Juan M. Cuerva, Giuseppe Mazzeo, Sandra Resa, Pablo Reiné, Andrea Lucotti, Luis Álvarez de Cienfuegos, Víctor Blanco, Matteo Tommasini, Santiago Guisán-Ceinos, Delia Miguel, Antonio J. Mota, Ana M. Ortuño, María Ribagorda, M. José Ruedas-Rama, Sergio Abbate, Araceli G. Campaña, Giovanna Longhi
Publikováno v:
Chemical communications (Cambridge, England). 54(99)
Here we describe a new class of CPL switches based on oxophilic interactions between chiral sulfoxide-containing ortho-phenylene ethynylene (o-OPE) foldamers and cationic metals. These systems represent a unique case combining high glum values (up to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81830b94fd3de4544588fef3a2b7fcff
https://pubmed.ncbi.nlm.nih.gov/30480686
https://pubmed.ncbi.nlm.nih.gov/30480686
Autor:
Giovanna Longhi, Juan M. Cuerva, M. Carmen Carreño, Diego J. Cárdenas, Santiago Guisán-Ceinos, María Ribagorda, Sergio Abbate, Luis Crovetto, Sandra Resa, Antonio J. Mota, Giuseppe Mazzeo, Delia Miguel, Luis Álvarez de Cienfuegos, Duane Choquesillo-Lazarte
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 24(11)
A new family of homochiral silver complexes based on carbophilic interactions with ortho-phenylene ethynylene (o-OPE) scaffolds containing up to two silver atoms are described. These compounds represent a unique class of complexes with chirality at t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dadfc15ad8e3df90a3c32f2c65e76fd5
https://pubmed.ncbi.nlm.nih.gov/29240981
https://pubmed.ncbi.nlm.nih.gov/29240981