谭斌（南科大教授）的个人简介
谭斌博士，2005年硕士毕业于厦门大学化学系。同年去新加坡留学，在新加坡南洋理工大学化学与生物化学系钟国富教授的指导下从事新型手性有机催化剂的设计合成及不对称domino反应的研究并于2010年3月取得博士学位。2010年3月至2012年9月，有幸在有机小分子催化领域的发源地之一美国The Scripps Research Institute，师从Barbas教授继续在此领域从事博士后研究。与此同时得到碳氢键活化大师YuJin-Quan教授的指点。2012年9月受聘为南方科技大学化学系副教授。最近两年，谭斌博士以第一作者身份发表1篇Nature Chemistry，2篇Journal of the American Chemical Society，2篇Angewandte Chemie International Edition。从2008年至今已经获批美国专利4项，发表30篇国外核心期刊SCI检索论文，其中14篇为第一作者，所有文章的影响因子全部大于5.5。研究领域
◆ 核心骨架结构导向的有机催化不对称合成
◆ 现代催化体系和绿色合成全新方法的开发
◆ 金属与有机催化组成的协同催化体系拓展
◆ 手性药物的开发和天然产物的策略全合成
工作经历
◆ 2010.3年至2012.9年，博士后, 美国斯克普斯研究所（The Scripps Research Institute）
◆ 2012年9月至今， 副教授， 南方科技大学化学系
学习经历
◆ 2010年，获得新加坡南洋理工大学哲学博士学位 (有机化学)
◆ 2005年，获得厦门大学理学硕士学位 (有机化学)
◆ 2001年，获得湖南科技大学理学学士学位 (化学教育)
所获荣誉
◆ 2013年，深圳市海外高层次人才“孔雀计划”入选者
◆ 2009年，国家优秀自费留学生奖学金
代表文章
1.Tan. B.; Toda N; Barbas III, C. F. Organocatalytic Amidation and Esterification of Aldehydes with Activating Reagents by a Cross-coupling Strategy. Angew. Chem. Int. Ed. 2012, 51, 12538-12541.
2.Tan. B.; Hernández-Torres, G.; Barbas III, C. F. Rational Design Enables Amide Nucleophiles for Organocatalytic Asymmetric Michael Reactions. Angew. Chem. Int. Ed. 2012, 51, 5381-5385.
3.Tan, B.; Zeng, X.; Leong, W. W. Y.; Shi, Z.; Barbas III, C.F.; Zhong, G. Core Structure-Based Design of a Novel Organocatalytic [3+2] Cycloaddition: Highly efficient and Stereocontrolled Synthesis of Spirocyclic Oxindoles. Chem. Eur. J. 2012, 18, 63-67.
4.Tan, B.; Candeias, N.; Barbas III, C.R. Construction of Bispirooxindoles Containing three Quaternary Stereocentres in a Cascade Using a Single Multifunctional Organocatalyst. Nature Chem. 2011, 3, 473-477.
5.Tan B.; Hernández-Torres, G.; Barbas III, C.F. J. Highly Efficient Hydrogen-Bonding Catalysis of the Diels-Alder Reaction of 3-Vinylindoles and Methyleneindolinones Provides Carbazolespirooxindole Skeleton. Am. Chem. Soc. 2011, 131, 12354-12358.
6.Tan, B.; Candeias, N.; Barbas III, C.F. J. Core-Structure-Motivated Design of a Phosphine-Catalyzed [3+2] Cycloaddition Reaction: Enantioselective Syntheses of Spirocyclopenteneoxindoles. Am. Chem. Soc. 2011, 131, 4672-4675.
7.Tan, B.; Zeng, X.; Chua, P. J.; Zhong, G. Rational Design of Domino Michael-Henry Reaction: Direct Construction of Bicyclo[3.2.1]octane Skeletons with Four Stereogeric Centers. Org. Lett. 2010, 12, 2682-2685.
8.Tan, B.; Zhu, D.; Zhang, L.; Dai, L.; Chua, P. J.; Shi, Z.; Zeng, X; Zhong, G. Water More than Just a Green Solvent: A Stereoselective One-Pot Access to All Chiral Tetrahydronaphthalenes in Aqueous Media. Chem. Eur. J. 2010, 16, 3842-3848.
9.Tan, B.; Shi. Z.; Chua, P. J.; Li, Y.; Zhong, G. Unusual Domino Michael/Aldol Condensation Reactions Employing Oximes as N-Selective Nucleophiles: Synthesis of N-Hydroxypyrroles. Angew. Chem. Int. Ed. 2009, 48, 758-761.
10.Tan, B.; Zhang, X.; Chua, P. J.; Zhong, G. Recyclable organocatalysis: highly enantioselective Michael addition of 1,3-diaryl-1,3-propanedione to nitroolefins (Cover Article). Chem. Commun. 2009, 779-781
11.Tan, B.; Zeng, X.; Lu, Y.; Chua, P. J.; Zhong, G. Rational Design of Organocatalyst: Highly Stereoselective Michael Addition of Cyclic Ketones to Nitroolefins. Org. Lett. 2009, 11, 1931-1933.
12.Tan, B.; Chua, P. J.; Zeng, X.; Lu, M.; Zhong, G. A Highly Diastereo- and Enantioselective Synthesis of Multisubstituted Cyclopentanes with Four Chiral Carbons by the Organocatalytic Domino Michael-Henry Reaction. Org. Lett. 2008, 10, 3489-3492.
13.Tan, B.; Shi, Z.; Chua, P. J.; Zhong, G. Control of Four Stereocenters in an Organocatalytic Domino Double Michael Reaction: Efficient Synthesis of Multisubstituted Cyclopentanes. Org. Lett. 2008, 10, 3425-3428.
14.Tan, B.; Chua, P. J.; Li, Y.; Zhong, G. Organocatalytic Asymmetric Tandem Michael-Henry Reactions: A Highly Stereoselective Synthesis of Multifunctionalized Cyclohexanes with Two Quaternary Stereocenters. Org. Lett. 2008, 10, 2437-2440.
美国专利
1.Zhong, G.; Tan, B.; Zhang, X.; Chua, P. J. Process for highly enantioselective Michael addition of 1,3-diaryl-1,3-propanedione to nitroolefins using using cinchona alkaloids as recyclable organocatalysts. U.S. Pat. Appl. Publ. (2012), US 20120004424 A1 20120105.
2.Zhong, G,; Tan, B.; Shi, Z. Chua, P. J. Process of forming pyrrole compounds. U.S. Pat. Appl. Publ. (2011), US 20110124881 A1 20110526.
3.Zhong, G,;Tan, B.; Chua, P. J.; Shi, Z. Process for preparation of chiral cycloalkane derivatives by asymmetric cyclization. U.S. Pat. Appl. Publ. (2010), US 20100298576 A1 20101125.
4.Zhong, G.; Lu, M.; Zhu, D.; Lu, Y.; Hou, Y.; Tan, B. Processes for enantioselective preparation of an aminoxy compound and an 1,2-oxazine compound. U.S. Pat. Appl. Publ. (2011), US 20110224429 A1 20110915
