Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Enzo Cereda"'
Publikováno v:
Tetrahedron Letters. 45:1413-1416
New insights into the cycloaddition reaction between alkyl isocyanides and benzyliden-1,3-diketones are reported. 5-Hydroxy-N-substituted-2H-pyrrol-2-ones and not substituted furans, as previously reported, are formed. The proof of the structure reli
Autor:
Ezhaya Antoine, Giovanbattista Schiavi, Angelo Sagrada, E. Bellora, Arturo Donetti, Henri Doods, Enzo Cereda
Publikováno v:
European Journal of Medicinal Chemistry. 29:411-421
A series of new 3-tropanol and 3-quinuclidinol esters of phenyl-substituted pyrrolidin-, piperidin- and azepin-2-oxocarboxylic acid were synthesized and tested for antimuscarinic activity. The compounds showed a preferential in vitro activity at M1 a
Publikováno v:
Tetrahedron Letters. 42:6827-6829
The Wittig reaction of a pool of stabilised ylides and aromatic aldehydes was carried out in a microwave oven. Only a few minutes were needed for high conversion rates under microwave heating in comparison to hour time with traditional methods.
Publikováno v:
Tetrahedron Letters. 42:4951-4953
[3+2] Cycloaddition of alkynes to resin bound nitrile oxides gives after cleavage of 3,4,5 trisubstituted isoxazoles in acceptable yields and fair to good purity, depending on the alkyne substituents. The reaction has been automated on the ACT 496 sy
Autor:
Giovanbattista Schiavi, Arturo Donetti, Enzo Cereda, Angelo Sagrada, Henri Doods, Ezhaya Antoine, E. Bellora
Publikováno v:
ChemInform. 25
A series of new 3-tropanol and 3-quinuclidinol esters of phenyl-substituted pyrrolidin-, piperidin- and azepin-2-oxocarboxylic acid were synthesized and tested for antimuscarinic activity. The compounds showed a preferential in vitro activity at M1 a
Publikováno v:
ChemInform. 32
Autor:
E. Bellora, Enrica Dubini, Arturo Donetti, Ezhaya Antoine, Giovanni Battista Schiavi, Alessandro Brambilla, Rosella Micheletti, Antonio Schiavone, Enzo Cereda, Myrna Gil Quintero
Publikováno v:
Journal of Medicinal Chemistry. 33:2108-2113
Amidines (guanidine, formamidine, and acetamidine) were introduced as substitutes for the cationic heads present in atropine, scopolamine, and corresponding quaternary derivatives. Amidine systems are intermediate in structure between tertiary amines
Publikováno v:
Journal of Receptor Research. 10:81-96
Guanylpirenzepine, a polar, non-quaternary analog of pirenzepine, exhibited a novel binding behavior in rat brain regions: in competition binding experiments against [3H]pirenzepine labeling the M1 receptor in membranes from cerebral cortex, hippocam
Publikováno v:
ChemInform. 38
Phenoxy benzyl ethers are easily and quickly deprotected in the presence of ammonium formate and microencapsulated Pd(0)EnCat with the assistance of microwave irradiation. This procedure can be applied in the presence of other functional groups as we
Publikováno v:
ChemInform. 37