欢迎本科生,硕士研究生和博士研究生加入我们课题组

化学楼E503,chengxu@nju.edu.cn

 

 

简历


程旭


1996.9-2000.8:
南开大学化学系,获得本科学位。
 

2000.9-2005.11:
南开大学元素有机化学研究所,师从周其林院士,获得博士学位,研究方向为金属有机手性催化剂的设计和对映选择性催化反应。
 

2005.12-2008.11:
德国Max-Planck煤炭研究所,从事博士后研究工作,研究方向为有机催化,Advisor:Benjamin List
 

2008.12-2009.12:
美国UT Austin,化学系从事博士后研究工作,研究方向为神经元修复活性的天然产物全合成,Advisor: Dionicio Siegel.
 

2010.1至今2012.6
美国Purdue University化学系博士后,研究方向为高抗癌活性天然产物全合成和抗SARS活性的药物设计,Advisor: Arun K. Ghosh. 
 

2012年7月:南京大学化学化工学院副教授

 

获奖: 2017 Thieme Chemistry Journal Award

 

  

 

 

发表论文:

   

 

 

 

Ph.D and Postdoctral Sessions:

 

 

 

天然和非天然产物的全合成; 有机催化; 金属有机催化

 

(1) Xu Cheng, Bing Zhou, Arun K. Ghosh*

Enantioselective Total Synthesis of (+)-Lithospermic Acid

Org. Lett. 2012, 14, 5046-5049

 

(2) Xu Cheng, RuLi, Bai, Arni Hamel, Arun K. Ghosh*,

Total Synthesis of Poetent Antitumor Macrolide, (-)-Zampanolide: An Oxidative C-H Bond Activation-Based Strategy.

Eur. J. Org. Chem. 2012, 4130

 

(3)  Xu Cheng, Arun K. Ghosh*

Synthesis of Functionalized 4-Methylenetetrahydropyrans by Oxidative C-H Activation of Allyl or Benzyl Ethers.

Tetrahedron Lett. 2012, 53, 2568-2570.

 

(4) Xu Cheng, Nicole L. Harzdorf, Zin Khaing, Danby Kang, Andrew M. Camelio, Travis Shaw, Christine E. Schmidt, and Dionicio Siegel*

Neuronal Growth Promoting Sesquiterpene-Neolignans;Syntheses and Biological Studies

Org. Biomol. Chem. 2012, 10, 383.

 

(5) Xu Cheng, Arun K. Ghosh*,   

Enantioselective Total Synthesis of (−)-Zampanolide, a Potent Microtubule-Stabilizing Agent

Org. Lett. 2011, 13, 4108. (one of most accessed papers in August)

 

(6) Xu Cheng, Nicole L. Harzdorf, Travis Shaw and Dionicio Siegel*

Biomimetic Syntheses of the Neurotrophic Natural Products Caryolanemagnolol and Clovanemagnolol

Org. Lett. 2010, 12, 1304.

 

(7) Xu Cheng, Sreekumar Vellalath, Richard Goddard, and Benjamin List*

Direct Catalytic Asymmetric Synthesis of Cyclic Aminals from Aldehydes

J. Am. Chem. Soc. 2008, 130, 15786.

 

(8) Nolwenn J. A. Martin, Xu Cheng, and Benjamin List*

Organocatalytic Asymmetric Transferhydrogenation of β-Nitroacrylates: Accessing β2-Amino Acids

J. Am. Chem. Soc. 2008, 130, 13862.

 

(9) Xu Cheng, Richard Goddard, Gernot Buth, Benjamin List*

Direct Catalytic Asymmetric Three-Component Kabachnik-Fields Reaction

Angew. Chem. Int. Ed. 2008, 47, 5079.

 

(10) Ji-Chao Yan, Xu Cheng, Qi-Lin Zhou*, and Jian Pei*

Chiral Polyfluorene Derivatives: Synthesis, Chiroptical Properties, and Investigation of the Structure−Property Relationships

Macromolecules, 2007, 40, 832.

 

(11) Xu Cheng, Jian-Hua Xie, Sheng Li, Qi-Lin Zhou*

Asymmetric Hydrogenation of a,b-Unsaturated Carboxylic Acids Catalyzed by Ruthenium(II) Complexes of Spirobifluorene Diphosphine (SFDP) Ligands 

Adv. Synth. Catal. 2006, 348, 1271.

 

(12) Xu Cheng, Shou-Fei Zhu, Xiang-Chen Qiao, Pu-Cha Yan, Qi-Lin Zhou*

A general synthetic route to chiral dihydroxy-9,9′-spirobifluorenes

Tetrahedron, 2006, 62, 8077.

 

(13) Jian-Hua Xie, Sheng Liu, Xiang-Hong Huo, Xu Cheng, Hai-Feng Duan, Bao-Min Fan, Li-Xin Wang, Qi-Lin Zhou*

Ru-II-SDP-complex-catalyzed asymmetric hydrogenation of ketones. Effect of the alkali metal cation in the reaction

J. Org. Chem. 2005, 70, 2967

 

(14) Xu Cheng , Qi Zhang, Jian-Hua Xie, Qi-Lin Zhou*

Highly Rigid Diphosphine Ligands with Large Dihedral Angle Based on Chiral Spirobifluorene Backbone

Angew. Chem. Int. Ed. 2005, 44, 1118

 

(15) Xu Cheng, Guo-Hua Hou, Jian-Hua Xie, Qi-Lin Zhou*

Synthesis and optical resolution of 9,9'-spirobifluorene-1, 1'-diol 
Org. Lett. 2004, 6, 2381

 

(16) Jian-Hua Xie, Hai-Feng Duan, Bao-Min Fan, Xu Cheng, Li-Xin Wang, Qi-Lin Zhou*

Application of SDP Ligands for Pd-catalyzed allylic alkylation 
Adv. Synth. Catal. 2004, 346, 625.

 

(17) Xiao-Guang Li, Xu Cheng, Qi-Lin Zhou*

A convenient synthesis of 2-alkyl-8-quinoline carboxylic acids

Synth. Commun. 2002, 32, 2477

 

(18) Xiao-Guang Li, Xu Cheng, Jun-An Ma, Qi-Lin Zhou*

Synthesis of chiral 2-alkyl-8-quinolinyl-oxazoline ligands: reversal of enantioselectivity in the asymmetric palladium-catalyzed allylic alkylation

J. Organomet. Chem. 2001, 640, 65