Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Vitalba Pace"'
Autor:
Francesca D'Anna, Vincenzo Frenna, Sandra La Marca, Renato Noto, Vitalba Pace, Domenico Spinelli
Publikováno v:
Tetrahedron. 64:672-680
In order to study the intrinsic characteristics and to evaluate the structural variations determined by the addition of a co-solvent to 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim][BF 4 ]) we examined the behaviour of some probes in [bmim][B
Publikováno v:
Tetrahedron. 62:1690-1698
The kinetics of the elimination reaction of 1,1,1-tribromo-2,2-bis(phenyl-substituted)ethanes into the corresponding 1,1-dibromo-2,2-bis(phenyl-substituted)ethenes induced by amines were studied in three room temperature ionic liquids ([BMIM][BF 4 ],
Autor:
Vitalba Pace, Stefano Morganti, G. Macaluso, Raffaella Spisani, V. Frenna, Domenico Spinelli, Francesca D'Anna, Patrizia Nitti
Publikováno v:
The Journal of Organic Chemistry. 69:8718-8722
The mononuclear rearrangement (MRH) of the Z-2,4-dinitrophenylhydrazone (4a) and of the Z-phenylhydrazone (4b) of 5-amino-3-benzoyl-1,2,4-oxadiazole into the relevant triazoles 5a and 5b in toluene has been quantitatively investigated in the presence
Publikováno v:
The Journal of organic chemistry. 71(26)
The kinetics of the rearrangement of the Z-phenylhydrazone of 3-benzoyl-5-phenyl-1,2,4-oxadiazole (1) into the relevant 4-benzoylamino-2,5-diphenyl-1,2,3-triazole (2) induced by amines have been studied in five room-temperature ionic liquids (RTILs)
Publikováno v:
The Journal of organic chemistry. 71(14)
The kinetics of the nucleophilic aromatic substitution of some 2-L-5-nitrothiophenes (para-like isomers) with three different amines (pyrrolidine, piperidine, and morpholine) were studied in three room-temperature ionic liquids ([bmim][BF4], [bmim][P
Autor:
Raffaella Spisani, Vincenzo Frenna, Susanna Guernelli, Fiammetta Ferroni, Camilla Zaira Lanza, Francesca D'Anna, Giovanni Petrillo, Gabriella Macaluso, Vitalba Pace, Domenico Spinelli
The rearrangement rates of several di-, tri-, tetra- or penta-substituted Z -arylhydrazones of 3-benzoyl-5-phenyl-1,2,4-oxadiazole ( 1a – 18a ) into the relevant 2-aryl-4-benzoylamino-5-phenyl-1,2,3-triazoles ( 1b – 18b ) have been determined in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e595c55e60c493e8549db988c78ae0bb
http://hdl.handle.net/11585/2552
http://hdl.handle.net/11585/2552
[reaction: see text] The kinetics of the rearrangement of the Z-phenylhydrazone of 3-benzoyl-5-phenyl-1,2,4-oxadiazole (1a) into the relevant 4-benzoylamino-2,5-diphenyl-1,2,3-triazole (2a) induced by amines have been studied in two room-temperature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffe808e073f9feb8571f5e93947bf744
http://hdl.handle.net/11585/2553
http://hdl.handle.net/11585/2553