開啟主選單

求真百科

1984年畢業於山東大學化學系, 1989年於中國科學院上海有機化學研究所獲博士學位, 1990-1994年在美國匹茲堡大學化學系和Mayo Clinic神經化學和神經生物學研究部進行博士後研究。 現任中國科學院上海有機化學研究所研究員,上海有機化學所副所長,復旦大學兼職教授 。

馬大為
出生 1963年9月
河南省社旗
國籍 中國
民族 漢族
職業 副所長、博導、研究員

目錄

研究方向

具有重要生理活性的複雜天然產物的全合成及結構-活性關係研究;針對特殊靶點如G-蛋白偶連受體,蛋白激酶,蛋白水解酶和細胞凋亡過程的小分子調節劑的發現;有機合成方法學的發展和其在合成生物活性分子中的應用。

獲獎及榮譽

上海市科技精英(2009) 國家自然科學二等獎 (2007); 上海市科學進步一等獎(2005); 上海市十大傑出青年(2001); 中國青年科技獎 (1998); 求是科技基金會傑出青年學者獎(1998);

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代表論文

1. Qian Cai, Benli Zou, Dawei Ma*, Mild Ullmann-type biaryl ether formation reaction via combination of ortho-substituent and ligand effects, Angew. Chem. Int. Ed. 2006, 45, 1276. 2. Dawei Ma*, Yongwen Jiang, Fangping, Chen, Li-kun, Gong, Ke Ding, Yong Xu, Renxiao Wang, Aihua Ge, Jin Ren*, Jingya Li, Jia Li and Qizhuang Ye, Selective inhibition of matrix metalloproteinase isozymes and in vivo protection against emphysema by substituted γ-keto carboxylic acids. J. Med. Chem. 2006, 49, 456. 3. Shouyun Yu, Xianhua Pan and Dawei Ma*, Total syntheses of halipeptins A-D, potent anti-inflammatory cyclic depsipeptides, Chem. Eur. J. 2006, 12, 6572. 4. Qian Cai, Gang He and Dawei Ma*, Mild and Non-racemization conditions for Ullmann-type diaryl ether formation between aryl halides and tyrosine derivatives, J. Org. Chem. 2006, 71, 5268. 5. Dawei Ma*, Bin Zou, Guorong Cai, Xiaoyi Hu and Jun O. Liu, Total synthesis of cyclodepsipeptide apratoxin A and its analogues and assessment of their biological activity, Chem. Eur. J. 2006, 12, 7615. 6. Shanghai Yu, Xiaotao Pu, Tiejun Cheng, Renxiao Wang and Dawei Ma*, Total Synthesis of Clavepictines A and B and Pictamine, Org. Lett. 2006, 8, 3179. 7. Xiaotao Pu and Dawei Ma*, Facile entry to decahydroquinoline alkaloids. Total synthesis of lepadins A-E and H, J. Org. Chem. 2006, 71, 6562. 8. Xiaoan Xie, Yu Chen, Dawei Ma, Enantioselective arylation of 2-methylacetoacetates catalyzed by CuI/trans-4-hydroxy-L-proline at low reaction temperature, J. Am. Chem. Soc. 2006, 128, 16050. 9. Dawei Ma,* Shanghai Yu, Ben Li,Li Chen,Renhai Chen, Kunqian Yu, Linqi Zhang, Zhiwei Chen, Dafang Zhong, Zheng Gong, Renxiao Wang, Hualiang Jiang and Gang Pei, Synthesis and biological evaluation of 1,3,3,4-tetrasubstituted pyrrolidine CCR5 receptor antagonists. Discovery of a potent and orally bioavailable anti-HIV agent. ChemMedChem. 2007, 2, 187-193. 10. Benli Zou, Qiliang Yuan, Dawei Ma*, 1,2-Disubstituted benzimidazoles by a Cu-catalyzed cascade aryl amination-condensation process, Angew. Chem. Int. Ed. 2007, 46, 2598. 11. Gang He, Jing Wang, Dawei Ma*, Highly convergent route to cyclopeptide alkaloids. Total synthesis of ziziphine N, Org. Lett. 2007, 9, 1367. 12. Zhankui Sun, Shouyun Yu, Zuoding Ding and Dawei Ma*, Enantioselective addition of activated terminal alkynes to 1-acylpyridinium salts catalyzed by u-bis(oxazoline) complexes, J. Am. Chem. Soc. 2007, 129, 9300. 13. Yu Chen, Xiaoan Xie and Dawei Ma*, Facile access to polysubstituted indoles via a cascade Cu-catalyzed arylation-condensation process, J. Org. Chem. 2007, 72, 9329. 14. Benli Zou, Qiliang Yuan, Dawei Ma*, Cascade coupling/cyclization process to N-substituted 1,3-dihydrobenzimidazol-2-ones, Org. Lett. 2007, 9, 4291. 15. Shaolin Zhu, Shouyun Yu, Dawei Ma*, Highly efficient catalytic system for enantioselective Michael addition of aldehydes to nitroalkenes in water,Angew. Chem. Int. Ed. 2008, 47, 545. 16. Yu Chen, Yuji Wang, Zheming Sun, Dawei Ma*, Elaboration of 2- (trifluoromethyl)-indoles via a cascade coupling-condensation-deacylation process, Org. Lett. 2008, 10, 625. 17. Weiqing Xie, Derong Ding, Weiwei Zi, Guangyu Li, Dawei Ma, Total synthesis and Structure of Papuamide B, a potent anti-HIV marine cyclodepsipeptide, Angew. Chem. Int. Ed. 2008, 47, 2844. 18. Li Tan, Dawei Ma, Total synthesis of salinamide A, a potent anti-inflammatory bicyclic depsipeptide, Angew. Chem. Int. Ed. 2008, 47, 3614. 19. Dawei Ma, Cai Qian, Copper/amino acid catalyzed cross-couplings of aryl and vinyl halides with nucleophiles, Acc. Chem. Res. 2008, 41, 1450. 20. Jing Wang, Anqi Ma, Dawei Ma, Organocatalytic Michael addition of aldehydes to γ-keto-α,β-unsaturated esters. An efficient entry to versatile chiral building blocks. Org. Lett. 2008, 10, 5425.

參考文獻

  1. 研究團隊 中國科學院生物與化學交叉研究中心