个人简历

教育经历\r
2009年9月-2012年7月，中国科学院上海药物研究所，理学博士\r
2006年9月-2009年7月，中国科学院上海药物研究所，理学硕士\r
2002年9月-2006年6月，南京大学，理学学士\r
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工作经历\r
2017年7月至今，中山大学化学学院，教授，博士生导师\r
2013年2月-2017年7月，新加坡南洋理工大学(Nanyang Technological University)，博士后（Research Fellow）\r
2012年7月-2013年2月，中国科学院上海药物研究所，助理研究员\r
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获奖情况\r
2014 上海市研究生优秀成果 \r
2013 中国科学院优秀博士学位论文\r
2012 中国科学院院长优秀奖 \r
2012 中国科学院优秀毕业生 \r
2013 浦东新区第七届优秀科技论文评选，学术类一等奖\r
2011 第一届亚洲青年有机化学前沿会议，最佳口头报告奖

研究领域

"""""电化学反应诱导的有机合成方法学，基于可控自由基反应的有机合成方法学，不对称催化"

近期论文

Mou, C.+, Zhu, T.+, Zheng, P., Yang, S., Song, B.-A.*, Chi, Y. R.* Green and Rapid Access to Benzocoumarins via Direct Benzene Construction through Base-Mediated Formal [4+2] Reaction and Air Oxidation. Adv. Synth. Catal. 2016, 358, 707-712\r
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Zhu, T., Mou, C., Li, B., Smetankova, M., Song, B-.A.* & Chi, Y. R.* N-heterocyclic carbene-catalyzed δ-carbon LUMO activation of unsaturated aldehydes. J. Am. Chem. Soc. 2015, 137, 5658. (highlighted by Synfacts 2015, 11, 0767)\r
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Zhu, T., Zheng, P., Mou, C., Yang, S., Song, B-.A. & Chi, Y. R.* Benzene construction via organocatalytif formal [3+3] cycloaddition reaction. Nature Commun. 2014, 5, 5027.\r
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Namitharan, K. +, Zhu, T. +, Cheng, J., Zheng, P., Li, X., Yang, S., Song, B.-A. & Chi, Y. R.* Metal and carbene organocatalytic relay activation of alkynes for stereoselective reactions. Nature Commun. 2014, 5, 3982\r
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Fu, Z., Xu, J., Zhu, T., Leong, W. W. Y. & Chi, Y. R. * β-Carbon activation of saturated carboxylic esters through N-heterocyclic carbene organocatalysts, Nature Chem. 2013, 5, 835-839.\r
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Zhu, T.-S., Jin, S.-S. & Xu, M.-H. * Rhodium-Catalyzed, Highly Enantioselective 1,2-Addition of Aryl Boronic Acids to α-Ketoesters and α-Diketones Using Simple, Chiral Sulful-Olefin Ligands. Angew. Chem. Int. Ed. 2012, 51, 780. (Highlighted by Synfacts, 2012, 8, 0422).\r
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Zhu, T.-S., Chen, J.-P. & Xu, M.-H. * Rhodium-Catalyzed Enantioselective Addition to Unsymmetrical α-Diketones: Tandem One-Pot Synthesis of Optical Active 3-Quaternary Isochroman Derivatives. Chem. Eur. J. 2012, 19, 865. (Highlighted by Synfacts, 2013, 9, 0360).\r
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Zhu, T.-S. & Xu, M.-H. * Efficient Synthesis of Optically Active α-Quaternary Amino Acids by Highly Diastereoselective [2,3]-Rearrangement of Allylic Ammonium Ylides. Chem. Commun. 2012, 48, 7274.\r
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Zhu, T.-S. & Xu, M.-H. * Chiral Sulfinamide-Olefin Ligands: swichable Selectivity in Rhodium-Catalyzed Asymmetric 1,2-Addition of Arylboronic Acids to Aliphatic α-Ketoesters. Chin. J. Chem. 2013, 31, 321.\r
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Su, L., Zhu, T.-S. & Xu, M.-H. * Indium-Mediated asymmetric intramolecular allenylation of N-tert- butanesulfinyl imines: efficient and practical access to chiral 3-allenyl-4-aminochromanes. Org. Lett. 2014, 16, 4118.\r
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Xu, J., Mou, C., Zhu, T., Song, B.-A. * & Chi, Y. R. * N-heterocyclic carbene-catalyzed chemoselective cross-aza-benzoin reaction of enals with isatin-derived ketimines: access to chiral quaternary aminooxindoles. Org. Lett. 2014, 16, 3272.\r
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Fu, Z., Jiang, K., Zhu, T., Torres, J. & Chi, Y. R. * Access to oxoquinoline heterocycles by N-heterocyclic carbene catalyzed ester activation for selective reaction with an enone. Angew. Chem. Int. Ed. 2014, 53, 6506-6510.\r
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Wang, H., Zhu, T.-S. & Xu, M.-H. * Rhodium-Catalyzed Enantioselective 1,2-Addition of Arylboronic Acids to Heteroaryl α-Ketoesters for Synthesis of Heteroaromatic α-Hydroxy Esters. Org. Biomol. Chem. 2012, 10, 9158. (Cover Article)\r
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Jin, S.-S., Wang, H., Zhu, T.-S. & Xu, M.-H.* Design of N-Cinnamyl Sulfinamides as New Sulful-containing Olefin Ligands for Asymmetric Catalysis: Achieving Structural Simplicity with a Categorical Linear Framework. Org. Biomol. Chem. 2012, 10, 1764. (Cover Article) (Highlighted by Synfacts, 2012, 8, 0651).\r
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Qi, W.-Y., Zhu, T.-S. & Xu, M.-H. * Design of Chiral Sulfoxide-Olefins as a New Class of Sulful-Based Olefin Ligands for Asymmetric Catalysis. Org. Lett. 2011, 13, 3410.\r
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Cheng, Y., Zou, X., Zhu, T. * Liu, Y., Zhang, S. & Huang, H. Synthesis and Characterization of Chiral Polymer Complexes Incorporating Polybinaphthyls, Bipyridine, and Eu(III) J. Polym. Sci. A: Polym. Chem. 2007, 45, 650.