D. Quagliato

发表

Silicon in synthesis. 21. Reagents for thiophenyl-functionalized cyclopentenone annulations and the total synthesis of (.+-.)-hirsutene

P. Magnus, D. Quagliato, 1985 .

The synthesis and structural characterization of way-120,491; a novel potassium channel activator

R. Soll, L. Humber, D. Engen, 1991 .

Efficient Procedure for the Reduction of α-Amino Acids to Enantiomerically Pure α-Methylamines

P. Andrae, E. Matelan, D. Quagliato, 2000 .

SILICON IN SYNTHESIS. 20. SYNTHESIS OF (.+-.)-HIRSUTENE USING ORGANOSILICON-MEDIATED TRANSFORMATIONS

P. Magnus, D. Quagliato, 1982 .

Design and SAR of novel potassium channel openers targeted for urge urinary incontinence. 2. Selective and potent benzylamino cyclobutenediones.

A. Gilbert, G. Francisco, T. Argentieri, 2000, Journal of medicinal chemistry.

Antihypertensive benzopyran-related potassium channel activators: a role for lipophilicity

R. Soll, D. Deininger, P. Dollings, 1991 .

Synthesis, physical properties, and antitumor activity of tetraplatin and related tetrachloroplatinum(IV) stereoisomers of 1,2-diaminocyclohexane.

V. Narayanan, R. Haugwitz, W. Anderson, 1986, Cancer treatment reports.

Naphthyl Tetronic Acids as Multi‐Target Inhibitors of Bacterial Peptidoglycan Biosynthesis

C. Caufield, R. Chopra, K. Svenson, 2007, ChemMedChem.

Use of structure-based drug design approaches to obtain novel anthranilic acid acyl carrier protein synthase inhibitors.

Dominick Quagliato, Diane Joseph-McCarthy, Elena Severina, 2005, Journal of medicinal chemistry.

Design and synthesis of aminohydantoins as potent and selective human β-secretase (BACE1) inhibitors with enhanced brain permeability.

M. Malamas, J. Erdei, K. Fan, 2010, Bioorganic & medicinal chemistry letters.

Design and SAR of novel potassium channel openers targeted for urge urinary incontinence. 1. N-Cyanoguanidine bioisosteres possessing in vivo bladder selectivity.

S. Antane, T. Argentieri, W. Spinelli, 2000, Journal of medicinal chemistry.