D. Andreotti

发表

Synthesis and pharmacological characterization of novel druglike corticotropin-releasing factor 1 antagonists.

A. Capelli, F. Blaney, S. Provera, 2008, Journal of medicinal chemistry.

Selective Inhibitors of G2019S-LRRK2 Kinase Activity.

H. Carlisle, J. Bright, K. Zobel, 2020, Journal of medicinal chemistry.

An Efficient Scalable Route for the Synthesis of Enantiomerically Pure tert-Butyl-(1R,4S,6R)-4-(hydroxymethyl)-3-azabicyclo[4.1.0]heptane-3-carboxylate

S. Provera, A. Ribecai, P. Stabile, 2010 .

A novel ketolide class: Synthesis and antibacterial activity of a lead compound.

S. Lociuro, A. Pozzan, E. Ratti, 2007, Bioorganic & medicinal chemistry letters.

GSK 2578215 A ; A potent and highly selective 2-arylmethyloxy-5-substitutent-N-arylbenzamide LRRK 2 kinase inhibitor

Darío, N. Gray, Xianming Deng, 2014 .

A specific and direct comparison of the trifluoromethyl and pentafluoro sulfanyl groups on the selective dopamine D(3) antagonist 3-(3-{[4-methyl-5-(4-methyl-1,3-oxazol-5-yl)-4H-1,2,4-triazol-3-yl]thio}propyl)-1-phenyl-3-azabicyclo[3.1.0]hexane template.

F. Micheli, S. Braggio, A. Checchia, 2010, Bioorganic & medicinal chemistry letters.

Discovery of 5-substituent-N-arylbenzamide derivatives as potent, selective and orally bioavailable LRRK2 inhibitors.

Zehong Wan, A. Reith, P. Bamborough, 2017, Bioorganic & medicinal chemistry letters.

Discovery of N-[(2S)-5-(6-fluoro-3-pyridinyl)-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamide, a novel clinical AMPA receptor positive modulator.

Paul W Smith, K. Thewlis, S. Ward, 2010, Journal of medicinal chemistry.

Regioselective synthesis of 1,3,5- and 1,3,4,5-substituted pyrazoles via acylation of N-Boc-N-substituted hydrazones

P. Righi, G. Rosini, D. Andreotti, 2011 .

Synthesis and biological evaluation of 4-alkoxysubstituted trinems. Part II

G. Gaviraghi, R. Fabio, T. Rossi, 1996 .

Synthesis and biological evaluation of 4-alkoxy substituted trinems. Part I

D. Donati, R. Fabio, T. Rossi, 1996 .

Synthesis and antibacterial activity of 4- and 8-methoxy trinems

G. Gaviraghi, E. D. Modugno, D. Donati, 1996 .

Synthesis and antibacterial, activity of 4-ureido trinems

S. Biondi, D. A. Pizzi, D. Andreotti, 1996 .

A New Sequential Intramolecular Cyclization Based on the Boekelheide Rearrangement

J. Klein, A. Mordini, D. Andreotti, 2011 .

Reaction of 2-alkyl pyridine N-oxide derivatives with Mosher’s acyl chloride: first example of stereoselective Boekelheide rearrangement

A. Pozzan, D. Andreotti, Arnaldo Nalin, 2010 .

The synthesis of enantiomerically pure, symmetrically substituted cyclopropane phosphonic acids — A constrained analog of the GABA antagonist phaclophen

A. Gomtsyan, S. Hanessian, L. Cantin, 1997 .

Synthesis and Structure − Activity Relationships of α ‐ Amino-γ-lactone Ketolides : A Novel Class of Macrolide Antibiotics

S. Lociuro, D. Donati, A. Paio, 2014 .

Structure-guided design of antibacterials that allosterically inhibit DNA gyrase.

Shruti Jain, R. Stavenger, K. Raha, 2019, Bioorganic & medicinal chemistry letters.

Asymmetric Synthesis of Enantiomerically Pure and Diversely Functionalized Cyclopropanes.

A. Gomtsyan, S. Hanessian, D. Andreotti, 1995 .

Synthesis of novel pentacyclic β-lactam antibacterial agents

S. Lociuro, G. Pain, D. Donati, 2000 .

A new versatile and diastereoselective synthesis of polysubstituted 2-oxopiperazines from naturally occurring amino acids

D. Donati, A. Paio, G. Reginato, 2007 .

Synthesis of new polysubstituted piperazines and dihydro-2H-pyrazines by selective reduction of 2-oxo-piperazines

D. Donati, A. Paio, A. Mordini, 2010 .

Synthesis and antibacterial activity of trinems bearing nitrogen derivatives at C(4)

D. Donati, S. Biondi, D. Andreotti, 1998 .

5- and 7-oxa trinems: their synthesis and biological evaluation

T. Rossi, C. Marchioro, D. Andreotti, 1996 .

Synthesis and Biological Evaluation of 4-Alkoxy Substituted Trinems. Part 1.

D. Donati, R. Fabio, T. Rossi, 1996 .

Synthesis and Biological Evaluation of 4-Alkoxysubstituted Trinems. Part 2.

G. Gaviraghi, R. Fabio, T. Rossi, 1996 .

Synthesis and Antibacterial Activity of 4‐ and 8‐Methoxy Trinems.

G. Gaviraghi, E. D. Modugno, D. Donati, 1996 .

Synthesis of novel 6-alpha and 6-beta-alkylcarbonylmethyl substituted penems.

G. Gaviraghi, G. Tarzia, D. Donati, 1995, The Journal of antibiotics.

Synthesis and Antibacterial Activity of 4-Ureido Trinems.

S. Biondi, D. A. Pizzi, D. Andreotti, 1997 .

Mechanism insights into an unexpected isomerisation reaction observed during conversion of N-benzyl piperazinones to corresponding N-benzyl thio-piperazinones

Elisa Moro, D. Andreotti, Arnaldo Nalin, 2011 .

GSK2578215A; a potent and highly selective 2-arylmethyloxy-5-substitutent-N-arylbenzamide LRRK2 kinase inhibitor.

N. Gray, Xianming Deng, H. Choi, 2012, Bioorganic & medicinal chemistry letters.

The squalestatins: decarboxy and 4-deoxy analogues as potent squalene synthase inhibitors.

C. Chan, B. Dymock, J. Scicinski, 1996, Journal of medicinal chemistry.

4''-O-(omega-Quinolylamino-alkylamino)propionyl derivatives of selected macrolides with the activity against the key erythromycin resistant respiratory pathogens.

S. Alihodžić, A. Hutinec, S. Lociuro, 2010, Bioorganic & medicinal chemistry.

Synthesis of 5-(3,4-dichlorophenyl)-4-[(methyloxy)methyl]-2-azabicyclo[3.2.1]octane derivatives as constrained aryl-piperidines with activity as triple re-uptake inhibitors

Francesco Ferroni, J. Klein, A. Paio, 2010 .

6-(3,4-dichlorophenyl)-1-[(methyloxy)methyl]-3-azabicyclo[4.1.0]heptane: a new potent and selective triple reuptake inhibitor.

K. Read, G. Tedesco, R. Carletti, 2010, Journal of medicinal chemistry.