Enzo Cereda

Boehringer Ingelheim (Italy) — Italy

Biochemistry, Genetics and Molecular Biology · Life Sciences

12h-index357citations39works0.02yr avg
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Research Topics

Receptor Mechanisms and Signaling(8), Synthesis and Reactions of Organic Compounds(7), Ion channel regulation and function(5), Chemical Synthesis and Reactions(5), Microwave-Assisted Synthesis and Applications(5)

Publications39 total

Fast Deprotection of Phenoxy Benzyl Ethers in Transfer Hydrogenation Assisted by Microwave.
ChemInform·2007
Fast deprotection of phenoxy benzyl ethers in transfer hydrogenation assisted by microwave
Tetrahedron Letters·2007· 21 cited
Microwaves in Organic Chemistry
ChemInform·2006
5-Hydroxy-2 H -pyrrol-2-ones and not 2-aminofurans are the cycloaddition products between alkyl isocyanides and benzyliden-1,3-diketones
Tetrahedron Letters·2004· 29 cited
ChemInform Abstract: Kinetic Study of Microwave‐Assisted Wittig Reaction of Stabilized Ylides with Aromatic Aldehydes.
ChemInform·2001
Kinetic study of microwave-assisted Wittig reaction of stabilised ylides with aromatic aldehydes
Tetrahedron Letters·2001· 29 cited
Solid-phase synthesis of 3-hydroxymethyl isoxazoles via resin bound nitrile oxides
Tetrahedron Letters·2001· 20 cited
ChemInform Abstract: New Pyrrolidin‐, Piperidin‐ and Azepin‐2‐oxocarboxylic Acid Esters are Preferential M1, M3 Muscarinic Antagonists. Synthesis and Bronchospasmolytic Activity.
ChemInform·1994
Antagonistic properties of McNeil‐A‐343 at 5‐HT<sub>4</sub> and 5‐HT<sub>3</sub> receptors
British Journal of Pharmacology·1994· 13 citedOpen Access
Medicinal chemistry of muscarinic agonists for the treatment of dementia disorders
European Journal of Drug Metabolism and Pharmacokinetics·1994· 7 cited
New pyrrolidin-, piperidin- and azepin-2-oxocarboxylic acid esters are preferential M1, M3 muscarinic antagonists. Synthesis and bronchospasmolytic activity
European Journal of Medicinal Chemistry·1994· 5 cited
Bronchospasmolytic activity of the novel muscarinic antagonist DAC 5889
Life Sciences·1993
New CCK antagonists derived from the amino acid residues of the CCK-8 fragment.
PubMed·1991· 1 cited
Synthesis and biological evaluation of new antimuscarinic compounds with amidine basic centers. A useful bioisosteric replacement of classical cationic heads
Journal of Medicinal Chemistry·1990· 23 citedOpen Access
Hexocyclium derivatives with a high selectivity for smooth muscle muscarinic receptors
British Journal of Pharmacology·1990· 13 citedOpen Access
Irreversible H2-antagonism of the four isomeric butyl analogues of mifentidine
Inflammation Research·1990
Affinitu profile of the novel muscarinic antagonist guanylpirenzepine
Life Sciences·1990· 8 cited
Guanylpirenzepine Distinguishes Between Neuronal m1 and m4 Muscarinic Receptor Subtypes
Journal of Receptor Research·1990· 3 cited
N-(Fluoroethyl)(imidazolylphenyl)formamidines. The issue of the active species of mifentidine
Journal of Medicinal Chemistry·1989· 12 cited
Are the imidazoles of cimetidine and mifentidine bioisostere?
European Journal of Medicinal Chemistry·1988· 4 cited
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Frequent Co-authors

A. Donetti(26), E. Bellora(17), Antoine Ezhaya(7), Monica Quai(7), R. Micheletti(6), Antonio Giachetti(4), A. Brambilla(4), G.B. Schiavi(4), A. Sagrada(4), Piero Del Soldato(3), Sara Frattini(3), Walter Barbaglia(3), Achille Schiavone(3), Eugenia Monferini(3), G. Bietti(3), H. Timmerman(3), Piercarlo Vanoni(2), Rosamaria Micheletti(2), Ferdinando Pagani(2), Enrica Dubini(2)