Institute of Marine Material Science & Technology
Shanghai Maritime University
1550 Haigang Avenue, Pudong District, Shanghai, 201306, China
Tel: 0086-21-38284811 (o)
Employment history:
n Shanghai Maritime University, 2009-
n Associate researcher, Shanghai Institute of Organic Chemistry, 2005-2008
n Assistant researcher, University of Hong Kong, 2004-2005
n Postdoctoral fellow, University of California at Santa Barbara , 2001-2004
n Postdoctoral fellow, Shanghai Institute of Organic Chemistry, 1999-2001
Education:
n Ph. D Zhejiang University (China) 1996-1999
n M.S. Dalian University of Technology (China) 1993-1996
n B. S. Wuhan Institute of Technology (China) 1989-1993
Publications:
1. Junhua Wang and Chaozhong Li, Cerium(IV) Ammonium Nitrate & Bromoethenyl)chlorodimethylsilane, in e-Encyclopedia of Reagents for Organic Synthesis （Edited by Leo A. Paquette，John Wiley & Sons, Ltd. 2008）.
2. A novel stereoseletive approach to (E)-vinylic selenides”
Junhua Wang, Xian Huang
Chin. Chem. Lett. 1999, 10, 437
Junhua Wang, Qing Xu, Xian Huang
J. Chem. Res-S 1999, 660
4. “Organic polyvalent iodine reagents-promoted coupling reaction of 1-alkynes”
Junhua Wang, Xian Huang
Chin. Chem. Lett. 1999, 10, 529
5. “A stereoselective synthesis of (E)-vinylseleno zirconocenes and (E)-vinylic selenol esters”
Xian Huang, Junhua Wang
Synlett 1999, 569
6. “Hydrozirconation of alkynyl(phenyl)iodonium salts and stereoselective synthesis of (E)-trisubstituted olefins”
Xian Huang, Junhua Wang and Deyu Yang
J. Chem. Soc., Perkin Trans. 1, 1999, 673.
7. “A stereoselective synthesis of (E)-divinyl diselenides and (E)-divinyl ditellurides”
Xian Huang, Junhua Wang
Synth. Commun. 2000, 30, 301
8. “A convenient and stereoselective synthesis of (E)-vinylic selenides”
Xian Huang, Junhua Wang
Synth. Commun. 2000, 30, 307
9. “A stereoselective approach to S-vinyl thioesters from alkynes, sulfur and acyl chlorides”
Wang Junhua, Xu Qing, Huang Xian
Chin. Chem. Lett. 2000, 11, 1
10. “Coupling of terminal alkynes promoted by organic polyvalent iodine compounds”
Xian Huang, Wang Junhua
Synth. Commun. 2000, 30, 9.
11. “Investigation of Bis(tributyltin)-Initiated Free Radical Cyclization Reactions of 4-Pentenyl Iodoacetates”
Junhua Wang and Chaozhong Li
J. Org. Chem. 2002, 67, 1271.
12. “Cycloaddition of o-qunione dimethides with p-quinol derivatives: regiocontrolled formation of anthracyclic ring systems”
Junhua Wang, Liping H. Pettus, and Thomas R. R. Pettus
Tetrahedron Lett. 2004, 45, 1793.
13. “A short diastereoselective synthesis of (+)-rishirilide B core structure”
Junhua Wang and Thomas R. R. Pettus
Tetrahedron Lett. 2004, 45, 5895.
14. “Synthesis of Pyrroles via Copper-Catalyzed Coupling of Amines with Bromoenones”
Yuanjia Pan, Hongjian Lu, Yewen Fang, Xinqiang Fang, Liqun Chen, Junlu Qian, Junhua Wang, Chaozhong Li
Synthesis 2007, 1242.
15. “Synthesis and Structural Revision of (±)-Laurentristich-4-ol”
Pinghong Chen, Junhua Wang*, Kun Liu, Chaozhong Li*
J. Org. Chem. 2008, 73, 339.
16. Clean Production of Acid Blue 9 via Catalytic Oxidation in Water
Junhua Wang and Honglin Wang
Ind. Eng. Chem. Res. 2009, 48, 5548.
17. Selective Decarboxylation: A Facile Synthesis of 3-Pyridinecarboxylic Acid Derivative
Junhua Wang and Honglin Wang
Synth. Commun. 2009, 39, 4139.
18. A Catalytic Synthesis of 3-Alkoxyacrylic Acid Esters under Neat Conditions
Junhua Wang and Honglin Wang
Synth. Commun. 2010, 40, 980.
19. Carbon dioxide capture under ambient conditions using 2-chloroethylamine.
Junhua Wang, Xiqin Zhang and Yun Zhou
Environmental Chemistry Letters, 2011, 9, 535.
4 Patents are in the process of examination.