Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Liliana B. Jimenez"'
Publikováno v:
ACS Omega. 7:21860-21867
Perylene derivatives constitute a promising class of compounds with technological applications mainly due to their optoelectronic properties. One mechanism proposed to synthesize them, starting from binaphthyl derivatives, is anionic cyclodehydrogena
Autor:
Andrés F. Cruz-Ortiz, Walter E. Olmedo, Gustavo A. Pino, Maximiliano Rossa, Philippe Maître, Liliana B. Jimenez
Publikováno v:
Journal of Physical Chemistry A
Journal of Physical Chemistry A, American Chemical Society, 2021, 125 (2), pp.607-614. ⟨10.1021/acs.jpca.0c09394⟩
The journal of physical chemistry. A
Journal of Physical Chemistry A, American Chemical Society, 2021, 125 (2), pp.607-614. ⟨10.1021/acs.jpca.0c09394⟩
The journal of physical chemistry. A
The present study reports the first structural characterization of protonated cyameluric acid ([CA + H]+) in the gas phase, which paves the way for prospective bottom-up research on the condensed-phase chemistry of CA in the protonated form. A number
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Perylene and its derivatives are some of the most interesting chromophores in the field of molecular design. One of the most employed methodologies for their synthesis is the cyclodehydrogenation of binaphthyls mediated by Lewis acids. In this articl
Autor:
Karina Fernanda Crespo Andrada, Adriana B. Pierini, Ronny Priefer, Diego M. Andrada, Federico Brigante, Liliana B. Jimenez, Marcelo Puiatti, Roberto A. Rossi
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
A new synthetic route to modify the cubane nucleus is reported here. Methyl-4-iodocubane-1-carboxylate (1) and 1,4-diiodocubane (2) were employed as reagents to react with arylthiolate and diphenylphosphanide ions under irradiation in liquid ammonia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fd956020a79bf357c57d812ab327322
https://pubs.rsc.org/en/content/articlelanding/2018/RA/C8RA06275G#!divAbstract
https://pubs.rsc.org/en/content/articlelanding/2018/RA/C8RA06275G#!divAbstract
Photoinduced Synthesis of Dibenzofurans: Intramolecular and Intermolecular Comparative Methodologies
The SRN1 reaction has been used as a powerful tool for the synthesis of heterocycles, and only a few studies about photoinduced intramolecular cyclization to generate a new C-O bond by a radical pathway have been reported. This work introduces two st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cc057d6cdca6df905846d687463624a
http://pubs.acs.org/doi/10.1021/acs.joc.8b00742
http://pubs.acs.org/doi/10.1021/acs.joc.8b00742
Publikováno v:
Chemical research in toxicology 20 (2007): 1820–1824. doi:10.1021/tx700282x
info:cnr-pdr/source/autori:Chatgilialoglu, Chryssostomos; Bazzanini, Rita; Jimenez, Liliana B.; Miranda, Miguel A./titolo:(5 ' S)-and (5 ' R)-5 ',8-cyclo-2 '-deoxyguanosine: Mechanistic insights on the 2 '-deoxyguanosin-5 '-yl radical cyclization/doi:10.1021%2Ftx700282x/rivista:Chemical research in toxicology/anno:2007/pagina_da:1820/pagina_a:1824/intervallo_pagine:1820–1824/volume:20
info:cnr-pdr/source/autori:Chatgilialoglu, Chryssostomos; Bazzanini, Rita; Jimenez, Liliana B.; Miranda, Miguel A./titolo:(5 ' S)-and (5 ' R)-5 ',8-cyclo-2 '-deoxyguanosine: Mechanistic insights on the 2 '-deoxyguanosin-5 '-yl radical cyclization/doi:10.1021%2Ftx700282x/rivista:Chemical research in toxicology/anno:2007/pagina_da:1820/pagina_a:1824/intervallo_pagine:1820–1824/volume:20
The two diastereomeric forms (5'S) and (5'R) of 5',8-cyclo-2'-deoxyguanosine have been synthesized and fully characterized. They have been used as references for the investigation of gamma-irradiation of 2'-deoxyguanosine and photolysis of 8-bromo-2'
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 2. :1092-1097
o-Iodohalobenzenes (X = I, Br, Cl) react in DMSO with the enolate ions of acetophenone, propiophenone and 1-(2-naphthyl)ethanone to afford mainly monosubstitution with retention of one halogen. The monosubstituted dehalogenated compounds are formed i
Publikováno v:
ChemInform. 45
A new one-pot synthetic route to achieve the preparation of hydroxy and amine binaphthyl and biphenanthryl aryls is here reported. This approach involves the reaction of 1,4-bromoiodobenzene, 4,4′-diiodobiphenyl, and 1,4- and 1,5-diiodonaphthalene
Publikováno v:
Organic & biomolecular chemistry 6 (2008): 1083–1086. doi:10.1039/b718222h
info:cnr-pdr/source/autori:Jimenez, Liliana B.; Encinas, Susana; Chatgilialoglu, Chryssostomos; Miranda, Miguel A./titolo:Solar one-way photoisomerisation of 5',8-cyclo-2'-deoxyadenosine/doi:10.1039%2Fb718222h/rivista:Organic & biomolecular chemistry/anno:2008/pagina_da:1083/pagina_a:1086/intervallo_pagine:1083–1086/volume:6
info:cnr-pdr/source/autori:Jimenez, Liliana B.; Encinas, Susana; Chatgilialoglu, Chryssostomos; Miranda, Miguel A./titolo:Solar one-way photoisomerisation of 5',8-cyclo-2'-deoxyadenosine/doi:10.1039%2Fb718222h/rivista:Organic & biomolecular chemistry/anno:2008/pagina_da:1083/pagina_a:1086/intervallo_pagine:1083–1086/volume:6
Under sunlight irradiation (5′S)-5′,8-cyclo-2′-deoxyadenosine 2 photoisomerises to the (5′R) isomer 1, which is the more easily repaired damage when these cyclopurine lesions are formed in DNA.
Autor:
Miguel A. Miranda, Chryssostomos Chatgilialoglu, Quinto G. Mulazzani, Maurizio Guerra, Mila D'Angelantonio, Liliana B. Jimenez, Marialuisa Russo
Publikováno v:
Chemistry-A European Journal 12 (2006): 7684–7693. doi:10.1002/chem.200600040
info:cnr-pdr/source/autori:Russo, M.; Jimenez, L. B.; Mulazzani, Q. G.; D'Angelantonio, M.; Guerra, M.; Miranda, M. A.; Chatgilialoglu, C./titolo:Chemical Radiation Studies of 8-Bromo-2'-deoxyinosine and 8-Bromoinosine in Aqueous Solutions/doi:10.1002%2Fchem.200600040/rivista:Chemistry-A European Journal/anno:2006/pagina_da:7684/pagina_a:7693/intervallo_pagine:7684–7693/volume:12
info:cnr-pdr/source/autori:Russo, M.; Jimenez, L. B.; Mulazzani, Q. G.; D'Angelantonio, M.; Guerra, M.; Miranda, M. A.; Chatgilialoglu, C./titolo:Chemical Radiation Studies of 8-Bromo-2'-deoxyinosine and 8-Bromoinosine in Aqueous Solutions/doi:10.1002%2Fchem.200600040/rivista:Chemistry-A European Journal/anno:2006/pagina_da:7684/pagina_a:7693/intervallo_pagine:7684–7693/volume:12
The reactions of hydrated electrons (e(aq) (-)) with 8-bromo-2'-deoxyinosine (8) and 8-bromoinosine (12) have been investigated by radiolytic methods coupled with product studies and have been addressed computationally by means of BB1K-HMDFT calculat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d359577f749389a4700446e639111deb