Dawei Ma
State Key Laboratory of Bioorganic and Natural Products Chemistry
Shanghai Institute of Organic Chemistry
Chinese Academy of Sciences
354 Fenglin Lu
China
Name/email consistency: medium
- Assembly of substituted phenothiazines by a sequentially controlled CuI/ L-proline-catalyzed cascade C-S and C-N bond formation. Ma, D., Geng, Q., Zhang, H., Jiang, Y. Angew. Chem. Int. Ed. Engl. (2010)
- Efficient and economical access to substituted benzothiazoles: copper-catalyzed coupling of 2-haloanilides with metal sulfides and subsequent condensation. Ma, D., Xie, S., Xue, P., Zhang, X., Dong, J., Jiang, Y. Angew. Chem. Int. Ed. Engl. (2009)
- Copper/amino acid catalyzed cross-couplings of aryl and vinyl halides with nucleophiles. Ma, D., Cai, Q. Acc. Chem. Res. (2008)
- Synthesis and biological evaluation of 1,3,3,4-tetrasubstituted pyrrolidine CCR5 receptor antagonists. Discovery of a potent and orally bioavailable anti-HIV agent. Ma, D., Yu, S., Li, B., Chen, L., Chen, R., Yu, K., Zhang, L., Chen, Z., Zhong, D., Gong, Z., Wang, R., Jiang, H., Pei, G. ChemMedChem (2007)
- Total synthesis of the cyclodepsipeptide apratoxin A and its analogues and assessment of their biological activities. Ma, D., Zou, B., Cai, G., Hu, X., Liu, J.O. Chemistry (2006)
- Selective inhibition of matrix metalloproteinase isozymes and in vivo protection against emphysema by substituted gamma-keto carboxylic acids. Ma, D., Jiang, Y., Chen, F., Gong, L.K., Ding, K., Xu, Y., Wang, R., Ge, A., Ren, J., Li, J., Li, J., Ye, Q. J. Med. Chem. (2006)
- Tetrahydroisoquinoline based sulfonamide hydroxamates as potent matrix metalloproteinase inhibitors. Ma, D., Wu, W., Yang, G., Li, J., Li, J., Ye, Q. Bioorg. Med. Chem. Lett. (2004)
- CuI-catalyzed coupling reaction of aryl halides with terminal alkynes in the absence of palladium and phosphine. Ma, D., Liu, F. Chem. Commun. (Camb.) (2004)
