今天是:2017年6月26日 星期一 农历六月初三
董琳 副教授(硕士生导师)
作者:佚名  来源:  发布时间:2016年01月01日  点击/评论:10098/0

董琳 副教授(硕士生导师)

联系方式

电话:028-85503538

E-mail: donglinscu@aliyun.com

成都市人民南路三段17# 四川大学华西药学院,610041

简历

1994-1998 郑州大学化学系,化学专业,理学学士

2001-2006 中国科学院成都有机化学研究所,有机化学专业,硕博连读,师从龚流柱教授

2006-2009 澳大利亚昆士兰大学化学系,博士后,师从Craig M. Williams教授

2009-2011 新加坡科技研究局化学与工程科学研究院,研究科学家,师从著名化学家K. C. Nicolaou 教授

2011-至今 四川大学华西药学院,副教授

获奖情况

12012 四川省“青年百人计划”海外高层次引进人才

22012 四川大学优秀青年骨干教师奖励

研究方向

1、  有机合成方法学研究

2、天然产物与药物合成

科研项目及成果

1、国家自然科学基金青年基金:3位季碳手性中心吲哚类天然产物及药物的全合成研究

 2013-2015项目负责人

发表论文

2011年以后

[1] Dong, L.*; Qu, C.-H.; Huang, J.-R.; Zhang, W.; Zhang, Q.-R.; Deng, J.-G. Rhodium-catalyzed Spirocyclic Sultam Synthesis by [3+2] Annulation with Cyclic N-Sulfonyl Ketimines and Alkynes, Chem. Eur. J. 2013, DOI: 10.1002/chem.201303372.

[2] Dong, L.*; Huang, J.-R.; Qu, C.-H.; Zhang, Q.-R.; Zhang, W.; Han, B.; Peng, C.* “Rhodium(III)-catalyzed vinylic sp2 C–H bond functionalization: efficient synthesis of pyrido[1,2-α]-benzimidazoles and imidazo[1,2-α]pyridines”, Org. Biomol. Chem. 2013, 11, 6142–6149.

[3] Huang, J.-R.; Zhang, Q.-R.; Qu, C.-H.; Sun, X.-H.; Dong, L.* Chen. Y.-C.* “Rhodium(III)-Catalyzed Direct Selective C(5)-H Oxidative Annulations of 2-Substituted Imidazoles and Alkynes by Double C-H Activation”,Org. Lett. 2013, 15, 1878-1881.

[4] Huang, J.-R.; Dong, L.*; Han, B.; Peng, C.*; Chen. Y.-C.* “Synthesis of Aza-Fused Polycyclic Quinolines via Double C-H Bond Activations, Chem. Eur. J. 2012, 18, 8896-8898.


2011
年以前

[1] Dong, L.; Deng, L.-J.; Lim, Y.-W.; Leung, G. Y.-C.; Chen, D. Y.-K.* Synthesis of Advanced Maoecrystal V Core Structure”, Chem. Eur. J. 2011, 17, 5778-5781.

[2] Nicolaou, K.-C.*; Dong, L.; Deng, L.-J.; Talbota, A. C.; Chen, D. Y.-K. “Synthesis of functionalized maoecrystal V core structures”, Chem. Commun. 2010, 46, 70-72.

[3] Dong, L.; Schill, H.; Grange, R. L.; Porzelle, A.; Johns, J. P.; Parsons, P. G.; Gordon, V. A.; Reddell, P. W.; Williams, C. M.* “Anticancer Agents from the Australian Tropical Rainforest: Spiroacetals EBC-23, 24, 25, 72, 73, 75 and 76”, Chem. Eur. J. 2009, 15, 11307-11318.

[4] Dong, L.; Gordon, V. A.; Grange, R. L.; Johns, J.; Parsons, P. G.; Porzelle, A.; Reddell, P.; Schill, H.; Williams, C. M.* “Synthesis of ent-EBC-23”, Highlight in Synfacts, 2009, 468.

[5] Dong, L.; Gordon, V. A.; Grange, R. L.; Johns, J.; Parsons, P. G.; Porzelle, A.; Reddell, P.; Schill, H.; Williams, C. M.* “Structure and Absolute Stereochemistry of the Anticancer Agent EBC-23 from the Australian Rainforest", J. Am. Chem. Soc. 2008, 130, 15262-15263.

[6] Dong, L.; Xu, Y.-J.; Gong, L.-Z.* “Rhodium-Catalyzed Asymmetric Nitroallylation of Arylmetallics with Cyclic Nitroallyl Acetates and Applications in Organic Synthesis”, Eur. J. Org. Chem. 2006, 4093-4105.

[7] Dong, L.; Xu, Y.-J.; Cun, L.-F.; Cui, X.; Mi, A.-Q.; Jiang, Y.-Z.; Gong, L.-Z.* “Asymmetric Nitroallylation of Arylboronic Acids with Nitroallyl Acetates Catalyzed by Chiral Rhodium Complexes and Its Application in a Concise Total Synthesis of Optically Pure (+)-g-Lycorane”, Org. Lett. 2005, 7, 4285-4288.

[8] Dong, L.; Xu, Y.-J.; Gong, L.-Z.*; Mi, A.-Q.; Jiang, Y.-Z. “Conjugate Additions of α, β-Unsaturated Ketones with Arylzinc Species That Form in Situ from Diethylzinc and Arylboronic Acids”, Synthesis2004, 7, 1057.

 



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