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Autor:
Giada Santin, Maria Grazia Bottone, Carlo Pellicciari, E. Fasani, U. De Simone, Giovanni Bottiroli, Anna Cleta Croce
Publikováno v:
Photochemical & Photobiological Sciences. 10:1783-1790
Photosensitizing molecules (PSs) undergo chemico-physical changes upon addition of suitable substituents, influencing both their photophysical properties and their ability to accumulate into cells. Once inside the cells, the modified PS acts as a flu
Autor:
Angelo Albini, E Fasani
Reviewing photo-induced processes that have relevance to a wide-ranging number of academic and commericial disciplines and interests covering chemistry, physics, biology and technology, this series is essential reading for anyone wishing to keep abre
Publikováno v:
Research on Chemical Intermediates. 28:231-237
UV irradiation of nifedipine leads to of triplet biradicals that can be detected by means of EPR spectroscopy.
Publikováno v:
Scopus-Elsevier
The photochemical behaviour of Trimethoprim, a trimethoxybenzylpyrimidine used as bactericide, in solution has been investigated. Direct irradiation causes a slow reaction (e.g. Φ in methanol 3 × 10 −4 ). The molecule is quite sensitive to benzyl
Publikováno v:
Journal of Heterocyclic Chemistry. 30:1041-1044
The absorption and fluorescence characteristics of 2(4-aminophenyl)pyrido[3,2-d]oxazole (1), of its thiazole 2 and imidazole 3 analogues, as well as of the corresponding pyrido[3,4-d]imidazole 4 have been examined. S 1 is a planar ππ * ICT state, s
Publikováno v:
ChemInform. 28
Publikováno v:
ChemInform. 28
Irradiation of the 6,8-difluoroquinolone antibiotic lomefloxacin causes selective heterolytic defluorination from position 8 and leads to products rationalized as arising from the cation either via nucleophile addition or intramolecular carbene C–H
Publikováno v:
Chemistry (Weinh., Print) 14 (2008): 653–663. doi:10.1002/chem.200701099
info:cnr-pdr/source/autori:M. Freccero, E. Fasani, M. Mella, I. Manet, S. Monti, A. Albini/titolo:Modeling the photochemistry of lomefloxacin, a reference phototoxic drug, by steady state and time-resolved experiments and DFT and post-HF calculations/doi:10.1002%2Fchem.200701099/rivista:Chemistry (Weinh., Print)/anno:2008/pagina_da:653/pagina_a:663/intervallo_pagine:653–663/volume:14
info:cnr-pdr/source/autori:M. Freccero, E. Fasani, M. Mella, I. Manet, S. Monti, A. Albini/titolo:Modeling the photochemistry of lomefloxacin, a reference phototoxic drug, by steady state and time-resolved experiments and DFT and post-HF calculations/doi:10.1002%2Fchem.200701099/rivista:Chemistry (Weinh., Print)/anno:2008/pagina_da:653/pagina_a:663/intervallo_pagine:653–663/volume:14
The irradiation in water of 1-ethyl-6,8-difluoro-7(3-methylpiperazino)3-quinolone-2-carboxylic acid (lomefloxacin), a bactericidal agent whose use is limited by its serious phototoxicity (and photomutagenicity in the mouse), leads to formation of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::2c77c9cf3c521d66a828a92d904af22f
https://publications.cnr.it/doc/169863
https://publications.cnr.it/doc/169863