J. Chang

发表

Discovery of (2E)-3-{2-butyl-1-[2-(diethylamino)ethyl]-1H-benzimidazol-5-yl}-N-hydroxyacrylamide (SB939), an orally active histone deacetylase inhibitor with a superior preclinical profile.

Kay Lin Goh, Z. Bonday, J. Wood, 2011, Journal of medicinal chemistry.

Transition-metal-catalyzed aminations and aziridinations of C-H and C=C bonds with iminoiodinanes.

J. Chang, P. Chan, Thi My Uyen Ton, 2011, Chemical record.

Copper(II) triflate catalyzed amination of 1,3-dicarbonyl compounds.

J. Chang, P. Chan, Thi My Uyen Ton, 2012, Chemistry.

Arabidopsis Monothiol Glutaredoxin, AtGRXS17, Is Critical for Temperature-dependent Postembryonic Growth and Development via Modulating Auxin Response*

K. Hirschi, Qingyu Wu, Sunghun Park, 2011, The Journal of Biological Chemistry.

Copper-catalyzed Ullmann coupling under ligand- and additive- free conditions. Part 1: O-Arylation of phenols with aryl halides

J. Chang, P. Chan, W. Chavasiri, 2008 .

Practical copper-catalyzed N-arylation of nitrogen heterocycles with aryl halides under ligand and additive free conditions

J. Chang, P. Chan, Xiuhui Xu, 2007 .

Scope of direct arylation of fluorinated aromatics with aryl sulfonates.

C. Chai, J. Chang, J. Seayad, 2012, Organic & biomolecular chemistry.

Highly efficient ruthenium(II) porphyrin catalyzed amidation of aldehydes.

J. Chang, P. Chan, 2008, Angewandte Chemie.

Iron(II)-catalyzed amidation of aldehydes with iminoiodinanes at room temperature and under microwave-assisted conditions.

J. Chang, P. Chan, Thi My Uyen Ton, 2011, The Journal of organic chemistry.

Practical Copper(I)‐Catalyzed Amidation of Aldehydes.

J. Chang, P. Chan, Thi My Uyen Ton, 2010 .

Practical copper(I)-catalysed amidation of aldehydes.

J. Chang, P. Chan, Thi My Uyen Ton, 2010, Chemical communications.

Copper iodide-catalyzed aziridination of alkenes with sulfonamides and sulfamate esters

J. Chang, P. Chan, Thi My Uyen Ton, 2009 .

N-Hydroxy-1,2-disubstituted-1H-benzimidazol-5-yl acrylamides as novel histone deacetylase inhibitors: design, synthesis, SAR studies, and in vivo antitumor activity.

Z. Bonday, Haishan Wang, Xukun Wang, 2009, Bioorganic & medicinal chemistry letters.

Scope of direct arylation of fluorinated aromatics with aryl sulfonates.

C. Chai, J. Chang, J. Seayad, 2012, Organic & biomolecular chemistry.

Transition-metal-catalyzed aminations and aziridinations of C-H and C=C bonds with iminoiodinanes.

J. Chang, P. Chan, Thi My Uyen Ton, 2011, Chemical record.

Development of new c-n bond formation strategies based on transition metal-catalyzed amidation and aziridination of activated c-h and c=c bonds.

J. Chang, 2010 .