Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Susana Encinas"'
Autor:
M. Consuelo Jiménez, Jorge C. Herrera-Luna, David Díaz Díaz, Susana Encinas, Alex Abramov, Raúl Pérez-Ruiz
Publikováno v:
Organic Letters
[EN] Heteroarene boronate esters constitute valuable intermediates in modern organic synthesis. As building blocks, they can be further applied to the synthesis of new materials, since they can be easily transformed into any other functional group. E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10e649dff1b64b11e89bec801786fad5
https://doi.org/10.1021/acs.orglett.1c00451
https://doi.org/10.1021/acs.orglett.1c00451
Autor:
Raúl Pérez-Ruiz, Jorge C. Herrera-Luna, David Díaz Díaz, Alex Abramov, Diego Sampedro, Susana Encinas, Consuelo Jiménez
We have witnessed during the last decade the great evolution that visible-light photoredox catalysis has experienced as a powerful tool in organic synthesis and formation of new compounds can be now tackle. In this context, generation of radical inte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10175::6d81f2a34ffce5ccf8ab65cb7ed41b30
https://investigacion.unirioja.es/documentos/641af343124b445f6ae671db
https://investigacion.unirioja.es/documentos/641af343124b445f6ae671db
Autor:
Miguel A. Miranda, Catia Clementi, Susana Encinas, Neus Duran-Giner, Fausto Elisei, Benedetta Carlotti
Publikováno v:
RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
instname
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC. Repositorio Institucional del CSIC
The singlet excited state of 4-nitroquinoline N-oxide ( NQNO*) has been characterized by different spectroscopic techniques, combining transient absorption with steady state and time-resolved emission spectroscopy. The energy of NQNO* has been establ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::098dfde150027c61f05e5eb077bc025c
http://hdl.handle.net/10251/160915
http://hdl.handle.net/10251/160915
Autor:
Susana Encinas Perea
Publikováno v:
Lecture Notes in Chemistry ISBN: 9783319316697
Solar filters, as photostable compounds, are used to protect the human skin against harmful UV radiation. Up until recently, sun protection was limited to the use of sunscreens whose active ingredients are UV filters, which reflect or absorb UV rays
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98da347bd276d443e1c3af0fb483867a
https://doi.org/10.1007/978-3-319-31671-0_11
https://doi.org/10.1007/978-3-319-31671-0_11
Publikováno v:
Organic Letters. 10:4409-4412
Photolysis of the title dyads under aerobic conditions leads to a 2-deoxyribonolactone derivative. Laser flash photolysis reveals that the process occurs from the short-lived benzophenone-like triplet excited state. A mechanism involving intramolecul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b397d966af7f7db11bf07dc4c5ea64f0
https://doi.org/10.1021/ol801514v
https://doi.org/10.1021/ol801514v
Autor:
Despoina Vrantza, Jean Cadet, Susana Encinas, Panagiotis Kaloudis, Michael Orfanopoulos, Miguel A. Miranda, Didier Gasparutto, Cecilia Paris, Leondios Leondiadis, Thanasis Gimisis, Georgios C. Vougioukalakis
Publikováno v:
Helvetica Chimica Acta. 89:2371-2386
The photochemistry of N-hydroxypyridine-2(1H)-thione (NHPT), inserted as a photolabile modifier at the 6-position of 2′-deoxyguanosine or guanosine, has been evaluated. In particular, 6-[(1-oxidopyridin-2-yl)sulfanyl]- (1a) and 6-[(pyridin-2-yl)sul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1a7cf51927b74c2a288342982b6b42d
https://doi.org/10.1002/hlca.200690220
https://doi.org/10.1002/hlca.200690220
Publikováno v:
Chemistry - A European Journal. 12:553-561
Time-resolved and product studies on the synthesized dyads 1 and 2 have provided evidence that the benzophenone-to-thymine orientation strongly influences intramolecular photophysical and photochemical processes. The prevailing reaction mechanism has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0b8262a67ff8c990cd9d4f8571e7c34
https://doi.org/10.1002/chem.200500345
https://doi.org/10.1002/chem.200500345
Autor:
Nadia Chouini-Lalanne, Miguel A. Miranda, Virginie Lhiaubet-Vallet, Jérôme Trzcionka, Susana Encinas
Publikováno v:
The Journal of Physical Chemistry B. 108:14148-14153
The detailed triplet state characteristics of 2-(4-acetylphenyl)isoindolin-1-one (kINP), a N-phenylphthalimidine (PPI) derivative, have been studied in fluid solution at room temperature. The attac...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c913b57f1485b84fddfee51beffd634
https://doi.org/10.1021/jp0498926
https://doi.org/10.1021/jp0498926
Publikováno v:
Chemical Research in Toxicology. 17:857-862
Time-resolved and product studies have shown that there is a strong interaction between drugs containing the benzophenone chromophore and the free thymidine nucleoside. In quantitative terms, such an interaction is stronger for the lowest lying npi*
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0deb11156a19561caa3a07857e29625d
https://doi.org/10.1021/tx034249g
https://doi.org/10.1021/tx034249g
Autor:
Emma R. Schofield, Catherine E. Housecroft, Lucia Flamigni, Francesco Barigelletti, Edwin C. Constable, Dieter Fenske, Margareta Zehnder, Markus Neuburger, Johannes G. Vos, Egbert Figgemeier, Susana Encinas
Publikováno v:
Chemistry - A European Journal. 8:137-150
The electronic absorption spectra, luminescence spectra and lifetimes (in MeCN at room temperature and in frozen n-C3H7CN at 77 K), and electrochemical potentials (in MeCN) of the novel dinuclear [(tpy)Ru(3)Os(tpy)]4+ and trinuclear [(tpy)Ru(3)Os(3)R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::572a96874dd71bbf0b442f3136726001
https://doi.org/10.1002/1521-3765(20020104)8:1<137::aid-chem137>3.0.co
https://doi.org/10.1002/1521-3765(20020104)8:1<137::aid-chem137>3.0.co