Zobrazeno 1 - 10
of 59
pro vyhledávání: '"María Ribagorda"'
Autor:
Estíbaliz Merino, María Ribagorda
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 1071-1090 (2012)
Control over molecular motion represents an important objective in modern chemistry. Aromatic azobenzenes are excellent candidates as molecular switches since they can exist in two forms, namely the cis (Z) and trans (E) isomers, which can interconve
Externí odkaz:
https://doaj.org/article/1c98badf8058431380149cdeb38cf92c
Autor:
Christian Cristóbal, Daniel Gaviña, Inés Alonso, María Ribagorda, Juan C. Carretero, Carlos del Pozo, Javier Adrio
Publikováno v:
Chemical Communications. 58:7805-7808
An enantioselective synthesis of polycyclic fluorinated pyrrolidines has been achieved by Cu-catalyzed intramolecular 1,3-dipolar cycloaddition of azomethine ylides with fluorinated dipolarophiles. The method displays a wide scope and afforded the de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be093a375eba8734c650da3024d599c4
https://doi.org/10.1039/d2cc02902b
https://doi.org/10.1039/d2cc02902b
Autor:
Gabriel López-Peña, Silvia Simón-Fuente, Dirk H. Ortgies, María Ángeles Moliné, Emma Martín Rodríguez, Francisco Sanz-Rodríguez, María Ribagorda
Publikováno v:
Cancers; Volume 15; Issue 1; Pages: 102
Functionalized upconverting nanoparticles (UCNPs) are promising theragnostic nanomaterials for simultaneous therapeutic and diagnostic purposes. We present two types of non-toxic eosin Y (EY) nanoconjugates derived from UCNPs as novel nanophotosensit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::785d81e07ae0a8469079c9a594e136a9
https://doi.org/10.3390/cancers15010102
https://doi.org/10.3390/cancers15010102
Autor:
Ana M. Ortuño, Sergio Abbate, Juan M. Cuerva, Luis Álvarez de Cienfuegos, Giovanna Longhi, Pablo Reiné, María Ribagorda, Antonio J. Mota, Sandra Resa, Delia Miguel
Publikováno v:
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Digibug. Repositorio Institucional de la Universidad de Granada
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Digibug. Repositorio Institucional de la Universidad de Granada
We thank the Ministerio de Economia y Competitividad (CTQ2017-85454-C2-1-P and CTQ2017-85454-C2-2-P), Ministerio de Ciencia e Innovacion (PID2020-113059GB-C21 and PID2020-113059GB-C22) and Junta de Andalucia (P20.00162) (Spain) for funding and P.R. a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::028f532bfd1a17fb51857e75c470cb10
https://hdl.handle.net/10486/704492
https://hdl.handle.net/10486/704492
Publikováno v:
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
instname
A straightforward methodology for the regioselective synthesis of pyrazoles has been developed by a domino sequence based on a photoclick cycloaddition followed by a photocatalyzed oxidative deformylation reaction. Distinguishing features of this pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a592da7d396c44d9abdabe0cd1da9590
https://pubmed.ncbi.nlm.nih.gov/34097415
https://pubmed.ncbi.nlm.nih.gov/34097415
Autor:
Ciro Rodríguez‐Diaz, Jaime Rojas-Martín, M. Carmen Carreño, Laura Ortiz-Rojano, María Ribagorda
Publikováno v:
Chemistry – A European Journal. 25:15050-15054
Quinones were firstly used as dipolarophiles in a photoclick 1,3-cycloaddition with 2,5-diaryltetrazoles, as photoactivatable predipoles, providing a novel and efficient access to three types of pyrazole-fused quinones (indazoledione derivatives). Di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bd685217fbbdd8424abd6a9409f8010
https://doi.org/10.1002/chem.201904138
https://doi.org/10.1002/chem.201904138
Publikováno v:
Org Lett
Described is a cross-electrophilic, deaminative coupling strategy harnessing Katritzky salts as a new species of electrophile in Ni/photoredox dual catalytic reductive cross-coupling reactions. Distinguishing features of this arylation protocol inclu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee7e2ce409b420d426245fe2e403517d
https://doi.org/10.1021/acs.orglett.9b01097
https://doi.org/10.1021/acs.orglett.9b01097
Autor:
Luis Álvarez de Cienfuegos, Juan M. Cuerva, María Ribagorda, Araceli G. Campaña, Giovanna Longhi, Sergio Abbate, Pablo Reiné, Angel Orte, José Justicia, Sara P. Morcillo, Delia Miguel, Belén Vaz
Publikováno v:
The Journal of Organic Chemistry
In this manuscript, we report the first synthesis of an organic monomolecular emitter, which behaves as a circularly polarized luminescence (CPL)-based ratiometric probe. The enantiopure helical ortho-oligo(phenylene)ethynylene ( o-OPE) core has been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5a6879e655c721bbb600146742a9668
https://doi.org/10.1021/acs.joc.8b00162
https://doi.org/10.1021/acs.joc.8b00162
Autor:
María Ribagorda, Laura Ortiz-Rojano, Carolina García-García, Mario Martínez-Mingo, M. Carmen Carreño
Publikováno v:
European Journal of Organic Chemistry. 2018:1034-1040
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8aae95a9c3bee1ec59b236a07434d643
https://doi.org/10.1002/ejoc.201701656
https://doi.org/10.1002/ejoc.201701656
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