Jizhou Wang

发表

Structure and inhibition of the drug-resistant S31N mutant of the M2 ion channel of influenza A virus

R. Lamb, M. Klein, W. DeGrado, 2013, Proceedings of the National Academy of Sciences.

Mixture of new sulfated steroids functions as a migratory pheromone in the sea lamprey

P. Sorensen, T. Hoye, Jizhou Wang, 2005, Nature chemical biology.

Enantioselective synthesis of structurally intricate and complementary polyoxygenated building blocks of Spongistatin 1 (Altohyrtin A)

D. Zuev, L. Paquette, Jizhou Wang, 2009 .

A Novel Method for Synthesizing Aldonophenylhydrazono-lactones

Lei Wang, Jizhou Wang, Peng Zhang, 1998 .

Relay ring-closing metathesis (RRCM): a strategy for directing metal movement throughout olefin metathesis sequences.

T. Hoye, Jizhou Wang, C. Jeffrey, 2004, Journal of the American Chemical Society.

Discovery of 5-pyrrolopyridinyl-2-thiophenecarboxamides as potent AKT kinase inhibitors.

J. Luengo, D. Yamashita, D. Heerding, 2009, Bioorganic & medicinal chemistry letters.

A modular approach to marine macrolide construction. 4. Assembly of C36-C51 and C29-C44 building blocks and evaluation of key coupling reactions targeting spongistatin 1 (altohyrtin A).

L. Paquette, Jizhou Wang, P. Forgione, 2007, Organic letters.

Unusual ligand-dependent chemoselective Suzuki–Miyaura cross-coupling reactions of 3-bromo-4-trifloyl-thiophenes

J. Luengo, Jizhou Wang, M. Seefeld, 2011 .

Discovery of novel dual inhibitors of the wild-type and the most prevalent drug-resistant mutant, S31N, of the M2 proton channel from influenza A virus.

R. Lamb, M. Klein, W. DeGrado, 2013, Journal of medicinal chemistry.

Details of the structure determination of the sulfated steroids PSDS and PADS: new components of the sea lamprey (petromyzon marinus) migratory pheromone.

P. Sorensen, T. Hoye, D. Muddiman, 2007, The Journal of organic chemistry.

Alkyne haloallylation [with Pd(II)] as a core strategy for macrocycle synthesis: a total synthesis of (-)-haterumalide NA/(-)-oocydin A.

T. Hoye, Jizhou Wang, 2005, Journal of the American Chemical Society.

Discovery of novel dual inhibitors of the wild-type and the most prevalent drug-resistant mutant, S31N, of the M2 proton channel from influenza A virus.

R. Lamb, M. Klein, W. DeGrado, 2013, Journal of medicinal chemistry.