Chen’s research group
Ph.D.

7.   Highly Enantioselective Desymmetrization of Meso- and Prochiral Cyclic Ketones via Organocatalytic Michael Reaction

J.-R. Chen, Y.-Y. Lai, H.-H. Lu, X.-F. Wang, W.-J. Xiao*

Tetrahedron 2009, 65, 9238-9243.

DOI: 10.1016/j.tet.2009.09.005

   
 
6.   Ru-Catalyzed Tandem Cross-Metathesis/ Intramolecular- Hydroarylation Sequence

J.-R. Chen, C.-F. Li, X.-L. An, J.-J. Zhang, X.-Y. Zhu, W.-J. Xiao*

Angew. Chem. Int. Ed. 2008, 47, 2489-2492.

DOI: 10.1002/anie.200705194

   
 
5.   Rational Combination of Two Privileged Chiral Backbones: Highly Efficient Organocatalysts for Asymmetric Direct Aldol Reactions Between Aromatic

J.-R. Chen, C.-F. Li, X.-L. An, J.-J. Zhang, X.-Y. Zhu, W.-J. Xiao*

J. Org. Chem. 2008, 73, 6006-600.

DOI: 10.1021/jo800910s

   
 
4.   Asymmetric Organocatalytic direct Aldol Reactions of Cyclohexanone with Aldehydes in Brine

W.-P. Huang, J.-R. Chen, X.-Y. Li, Y.-J. Cao, W.-J. Xiao*

Can. J. Chem. 2007, 85, 208-213.

DOI: 10.1139/v07-012

   
 
3.   Organocatalytic Asymmetric Aldol Reaction of Ketones with Isatins: Straightforward Stereoselective Synthesis of 3-Alkyl-3-hydroxyindolin-2-ones

J.-R. Chen, X.-P. Liu, X.-Y. Zhu, L. Li, Y.-F. Qiao, J.-M. Zhang, W.-J. Xiao*

Tetrahedron 2007, 63, 10437-10444.

DOI: 10.1016/j.tet.2007.08.003

   
 
2.   Sterically and Electronically Tunable and Bifunctional Organocatalysts: Design and Application in Asymmetric Aldol Reaction of Cyclic Ketones

J.-R. Chen, X.-Y. Li, X.-N. Xing, W.-J. Xiao*

J. Org. Chem. 2006, 71, 8198-8202.

DOI: 10.1021/jo0615089

   
 
1.   Sterically and Electronically Tunable and Bifunctional Organocatalysts: Design and Application in Asymmetric Aldol Reaction of Cyclic Ketones

J.-R. Chen, H.-H. Lu, X.-Y. Li, L. Cheng, J. Wan, W.-J. Xiao*

Org. Lett. 2005, 7, 4543-4545.

DOI: 10.1021/ol0520323

   
 

Key Laboratory of Pesticide & Chemical Biology, Ministry of Education             CCNU-uOttawa Joint Research Centre on Catalysis & Synthesis

Webmaster : chenjiarong@mail.ccnu.edu.cn

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