Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Maria Concetta Natoli"'
Autor:
Gianfranco Fontana, Felice Filizzola, Leopoldo Ceraulo, David Bongiorno, Maria Concetta Natoli
Publikováno v:
Rapid Communications in Mass Spectrometry. 20:3081-3088
The electron ionization (EI)-induced fragmentations of a series of 1,1-(2,2'-dimethoxyphenyl)-substituted 2-methylpropanes (1-20) in both 70 eV and mass-analyzed ion kinetic energy (MIKE) spectra have been investigated. The EI-MS spectra of these com
Autor:
Liliana Lamartina, Felice Filizzola, Gianfranco Fontana, Leopoldo Ceraulo, Maria Concetta Natoli
Publikováno v:
ARKIVOC, Vol 2002, Iss 11, Pp 123-141 (2002)
Publikováno v:
Journal of Physical Organic Chemistry. 15:108-114
The methoxide-promoted elimination reaction of some 1,1,1-trichloro-2,2-bis(phenyl-substituted)ethanes (1) was investigated. The ortho-substituted derivatives were found to be less reactive than the corresponding ortho-unsubstituted derivatives, irre
Publikováno v:
Rapid Communications in Mass Spectrometry. 14:203-206
The behaviour of some ortho-alkylhetero-substituted diphenylcarbinols, including deuterium labelled derivatives, under chemical ionisation (methane or isobutane) conditions has been investigated. It has been determined that ortho-alkylhetero diphenyl
Autor:
Renato Noto, Maria Concetta Natoli, Vincenzo Frenna, Gianfranco Fontana, Michelangelo Gruttadauria
Publikováno v:
Scopus-Elsevier
The base–promoted elimination reactions of 1,1,1-trichloro-2,2-bis(dimethoxyphenyl)ethanes were investigated. The bis(3,4-dimethoxyphenyl)ethane was found to be more reactive than the bis(2,5-dimethoxyphenyl)ethane and the latter more reactive than
Publikováno v:
ChemInform. 25
Autor:
Mirella Ferrugia, Liliana Lamartina, Pasquale Agozzino, Leopoldo Ceraulo, Maria Concetta Natoli
Publikováno v:
Organic Mass Spectrometry. 27:1127-1130
The hydrogen-carbon, carbon-carbon double rearrangement, responsible for the formation of benzyl or tropylium ions previously observed in the electron ionization mass spectra of several substituted 1,1-bis(dimethoxydiphenyl)methanes bearing an ortho
Autor:
Pasquale Agozzino, Mirella Ferrugia, Maria Concetta Natoli, Leopoldo Ceraulo, Liliana Lamrtina
Publikováno v:
Organic Mass Spectrometry. 26:857-861
The 75 eV electron impact mass spectra of 1,1-bis(dimethoxyphenyl)methanes bearing o-methoxy groups are dominated by intense peaks corresponding, at least formally, to benzyl ions [(CH3O)2C6H3CH2]+(b). They arise from ions [((CH3O)2C6H3)2CH]+(a), whi
Autor:
Liliana Lamartina, Leopoldo Ceraulo, Maria Concetta Natoli, Mirella Ferrugia, Pasquale Agozzino
Publikováno v:
Organic Mass Spectrometry. 26:279-286
The electron impact-induced fragmentations of 23 9,10-disubstituted 2,3,6,7-tetraalkoxy-9,10-dihydroanthracenes, including six stereoisomeric pairs, were studied. The loss of the 9-(or 10-)substituent constitutes the main fragmentation route. The res
Autor:
Maria Concetta Natoli, David Bongiorno, Giuseppe Avellone, Luisa Tesoriere, Felice Filizzola, Maria A. Livrea, Pasquale Agozzino, Leopoldo Ceraulo
Oxidation of melatonin by Fenton reagents as well as with hypochlorous acid or oxoferryl hemoglobin has been investigated. Analysis of products by low resolution/mass spectra (MS), high resolution/MS, 1H-nuclear magnetic resonance (NMR), 13C-NMR, cor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ba6e410ff902e4f37cf7722af480019
http://hdl.handle.net/10447/243627
http://hdl.handle.net/10447/243627