Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Giovanna Padova"'
Autor:
A. Depaoli, Elvio Bellasio, F. Battaglia, Romeo Ciabatti, Domenico Barone, E. Baldoli, Giorgio Tarzia, Mario Cellentani, Giovanna Padova
Publikováno v:
Journal of medicinal chemistry. 29(3)
The synthesis of 1-[(2-mercaptocyclopentyl)carbonyl]-L-prolines, 1-[(2-mercaptocyclobutyl)carbonyl]-L-prolines and related benzoyl derivatives as pure isomers is described. The abilities of all the compounds to inhibit angiotensin converting enzyme (
Autor:
Romeo Ciabatti, Giulio Galliani, F. Battaglia, Giuseppe Spina, Pierfranco Schiatti, Mario Cellentani, Giovanna Padova, U. Guzzi, A. Depaoli
Publikováno v:
Journal of medicinal chemistry. 29(10)
The synthesis of the pure diastereoisomer of 16-methoxy-16-methyl-PGF2 alpha, -PGE2, and -PGE1 is described. The absolute configuration of C-16 was established by chemical methods, while the absolute C-15 configurations of the diastereoisomers were a
Autor:
Romeo Ciabatti, Giulio Galliani, U. Guzzi, F. Battaglia, Mario Cellentani, Giovanna Padova, Giuseppe Spina, Pierfranco Schiatti, A. Depaoli
Publikováno v:
ChemInform. 18
The synthesis of the pure diastereoisomer of 16-methoxy-16-methyl-PGF2 alpha, -PGE2, and -PGE1 is described. The absolute configuration of C-16 was established by chemical methods, while the absolute C-15 configurations of the diastereoisomers were a
Autor:
F. Battaglia, Giovanna Padova, E. Baldoli, Domenico Barone, Elvio Bellasio, Giorgio Tarzia, Romeo Ciabatti, A. Depaoli, Mario Cellentani
Publikováno v:
Chemischer Informationsdienst. 17
The synthesis of 1-[(2-mercaptocyclopentyl)carbonyl]-L-prolines, 1-[(2-mercaptocyclobutyl)carbonyl]-L-prolines and related benzoyl derivatives as pure isomers is described. The abilities of all the compounds to inhibit angiotensin converting enzyme (
Publikováno v:
Journal of Heterocyclic Chemistry. 14:947-948
Treatment of amides 1a,b with thionyl chloride followed by reaction with triethylamine gave 1,4-dihydro[1]benzopyrano[4,3-b]pyrrole derivatives (4a,b) arising from intramolecular 1,3-cycloaddition of intermediate nitrile ylides (3a,b).