J. O'Brien

发表

Parallel synthesis of prostaglandin E1 analogues.

J. Ellman, L. Thompson, D. Dragoli, 1999, Journal of combinatorial chemistry.

Synthesis of novel HIV-1 protease inhibitors based on carbohydrate scaffolds

Amos B. Smith, J. O'Brien, P. Murphy, 2003 .

Characterization of thien-2-yl 1S,2R-milnacipran analogues as potent norepinephrine/serotonin transporter inhibitors for the treatment of neuropathic pain.

Beth A. Fleck, Rebecca R. Pick, M. Bradbury, 2008, Journal of medicinal chemistry.

Synthesis of peptidomimetics based on iminosugar and β-d-glucopyranoside scaffolds and inhibiton of HIV-protease

J. O'Brien, P. Murphy, L. Cronin, 2004 .

A simple and effective separation and purification procedure for DNA fragments using Dodecyltrimethylammonium bromide

K. Dawson, D. McLoughlin, J. O'Brien, 2000, Bioseparation.

A general synthesis of iminosugars.

C. McDonnell, J. O'Brien, P. Murphy, 2004, Journal of Organic Chemistry.

Novel synthesis of the glycosidase inhibitor deoxymannojirimycin and of a synthetic precursor D-lyxo-hexos-5-ulose.

J. O'Brien, P. Murphy, M. Tosin, 2001, Organic letters.

Stereospecific synthesis of β-d-allopyranosides by dihydroxylation of β-d-erythro-2,3-dideoxyhex-2-enopyranosides

Amos B. Smith, J. O'Brien, P. Murphy, 2001 .

Structure-based design and synthesis of HIV-1 protease inhibitors employing beta-D-mannopyranoside scaffolds.

Amos B. Smith, J. O'Brien, P. Murphy, 2002, Bioorganic & medicinal chemistry letters.

Characterization of thien-2-yl 1S,2R-milnacipran analogues as potent norepinephrine/serotonin transporter inhibitors for the treatment of neuropathic pain.

Beth A. Fleck, Rebecca R. Pick, M. Bradbury, 2008, Journal of Medicinal Chemistry.