Zobrazeno 1 - 10
of 26
pro vyhledávání: '"M L, Bajardi"'
Autor:
Giuseppe Daidone, Demetrio Raffa, Gabriella Bombieri, Benedetta Maggio, M. L. Bajardi, F. Benetollo, Domenico Schillaci, Salvatore Plescia
Publikováno v:
European Journal of Medicinal Chemistry. 31:461-468
Summary A number of new 4-diazopyrazole derivatives were prepared by the reaction of 1- R -3-methyl-5(R 1 -substituted)benzamidopyrazoles with a sevenfold excess of nitrous acid in acetic medium. The compounds were tested for activity against Escheri
Publikováno v:
Archiv der Pharmazie. 328:705-708
A number of 2-([(phenoxy or phenyl)acetyl]amino)benzoic acid derivatives were prepared in about 50% yield from (phenoxy or phenyl)acetyl chloride and anthranilic acid derivatives. All the compounds were tested as in vitro inhibitors of 3 alpha-hydrox
Autor:
Vmc Cutuli, Benedetta Maggio, Demetrio Raffa, M. Amico-Roxas, Salvatore Plescia, A. Caruso, Giuseppe Daidone, M. L. Bajardi
Publikováno v:
European Journal of Medicinal Chemistry. 29:707-711
A number of new ethyl 1-methyl-5-[4-oxo-3(4 H )-quinazolinyl]-1 H -pyrazole-4-acetates substituted at the 2 position of the quinazolinone ring were prepared. The compounds were tested for analgesic and antiinflammatory activities, as well as for thei
Autor:
A. Roccaro, Vincenza Maria Catena Cutuli, A. Caruso, E. Di Pietro, Giuseppe Daidone, M. L. Bajardi, Demetrio Raffa
Publikováno v:
ChemInform. 23
Publikováno v:
ChemInform. 23
The fragmentation reactions induced by electron impact of eighteen title compounds has been investigated with the aid of low beam energy spectra (14 eV, nom. value), metastable ion detection, high resolution measurements and labelling experiments. Th
Publikováno v:
ChemInform. 25
Publikováno v:
ChemInform. 26
By reacting l-R1-3-R2-5-(R3-substituted)benzamidopyrazoles with a great ex-cess of nitrous acid in acetic acid media, the related 4-diazoderivatives in 65–80% yields were obtained.
Publikováno v:
ChemInform. 27
A number of 2-([(phenoxy or phenyl)acetyl]amino)benzoic acid derivatives were prepared in about 50% yield from (phenoxy or phenyl)acetyl chloride and anthranilic acid derivatives. All the compounds were tested as in vitro inhibitors of 3 alpha-hydrox
Autor:
Giuseppe Daidone, Benedetta Maggio, F. Benetollo, M. L. Bajardi, Gabriella Bombieri, Salvatore Plescia, Domenico Schillaci, Demetrio Raffa
Publikováno v:
ChemInform. 27
Summary A number of new 4-diazopyrazole derivatives were prepared by the reaction of 1- R -3-methyl-5(R 1 -substituted)benzamidopyrazoles with a sevenfold excess of nitrous acid in acetic medium. The compounds were tested for activity against Escheri
Publikováno v:
Journal of Heterocyclic Chemistry. 29:565-568
The fragmentation reactions induced by electron impact of eighteen title compounds has been investigated with the aid of low beam energy spectra (14 eV, nom. value), metastable ion detection, high resolution measurements and labelling experiments. Th