Audrey Wong

发表

A rapid synthesis of 2-aryl-5-substituted-2,3-dihydrobenzofurans.

Jeffrey T. Kuethe, I. Davies, M. Journet, 2005, The Journal of organic chemistry.

Synthesis of 5-substituted-1H-indol-2-yl-1H-quinolin-2-ones: a novel class of KDR kinase inhibitors.

I. Davies, D. Hughes, J. Kuethe, 2005, The Journal of organic chemistry.

Synthesis and Resolution of Quinazolinone Atropisomeric Phosphine Ligands(,).

X. Dai, S. Virgil, Audrey Wong, 1998, The Journal of organic chemistry.

Synthesis of novel KDR kinase inhibitors through catalytic reductive cyclization of o-nitrobenzylcarbonyl compounds.

I. Davies, D. Hughes, J. Kuethe, 2004, The Journal of organic chemistry.

Synthesis of disubstituted imidazo[4,5-b]pyridin-2-ones.

I. Davies, J. Kuethe, Audrey Wong, 2004, The Journal of organic chemistry.

Aza-Diels–Alder/intramolecular Heck cyclization approach to the tetrahydro-β-carboline skeleton of the ajmaline/sarpagine alkaloids

I. Davies, P. Reider, J. Kuethe, 2002 .

Stereoselective preparation of a cyclopentane-based NK1 receptor antagonist bearing an unsymmetrically substituted sec-sec ether.

I. Davies, D. Hughes, P. Dormer, 2006, The Journal of organic chemistry.

Rapid and efficient synthesis of 1H-indol-2-yl-1H-quinolin-2-ones.

Jeffrey T. Kuethe, I. Davies, J. Kuethe, 2003, Organic letters.

Effective strategy for the preparation of indolocarbazole aglycons and glycosides: total synthesis of tjipanazoles B, D, E, and I.

I. Davies, J. Kuethe, Audrey Wong, 2003, Organic letters.

Effective strategy for the preparation of indolocarbazole aglycons and glycosides: total synthesis of tjipanazoles B, D, E, and I.

I. Davies, J. Kuethe, Audrey Wong, 2003, Organic letters.

A general synthesis of N-hydroxyindoles.

I. Davies, J. Kuethe, Audrey Wong, 2003, The Journal of organic chemistry.

Asymmetric synthesis of 1,2,3-trisubstituted cyclopentanes and cyclohexanes as key components of substance p antagonists.

C. Welch, I. Davies, P. Reider, 2002, The Journal of organic chemistry.

Reactive resin facilitated preparation of an enantiopure fluorobicycloketone.

C. Welch, I. Davies, D. Hughes, 2004, Organic & biomolecular chemistry.