Chen’s research group
2010

15.   Enantioselective Conjugate Addition of Oximes to Trisubstituted beta-Nitroacrylates: An Organocatalytic Approach to beta(2,2)-Amino Acid DerivativesF.

F.-G. Zhang, Q.-Q. Yang, J. Xuan, H.-H. Lu, S.-W. Duan, J.-R. Chen*, W.-J. Xiao*

Org. Lett. 2010, 12, 5636-5639.

DOI: 10.1021/ol102580n

   
 
14.   Organocatalytic Asymmetric Sulfa-Michael/Michael Addition Reactions: A Strategy for the Synthesis of Highly Substituted Chromans with a Quaternary

X.-F. Wang, Q.-L. Hua, Y. Cheng, X.-L. An, Q.-Q. Yang, J.-R. Chen*, W.-J. Xiao*

Angew. Chem. Int. Ed. 2010, 49, 8379-8383.

DOI: 10.1002/anie.201004534

   
 
13.   An Enantioselective Approach to Highly Substituted Tetrahydrocarbazoles through Hydrogen Bonding-Catalyzed Cascade Reactions

X.-F. Wang, J.-R. Chen, Y.-J. Cao, H.-G. Cheng, W.-J. Xiao*

Org. Lett. 2010, 12, 1140-1143.

DOI: 10.1021/ol1001818

   
 
12.   Tuning Electronic and Steric Effects: Highly Enantioselective [4 + 1] Pyrroline Annulation of Sulfur Ylides with alpha,beta-Unsaturated Imines

L.-Q. Lu, J.-J. Zhang, F. Li, Y. Cheng, J. An, J.-R. Chen*, W.-J. Xiao*

Angew. Chem. Int. Ed. 2010, 49, 4495-4498.

DOI: 10.1002/anie.201000755

   
 
11.   Highly Enantioselective Michael Addition of Aldehydes to Nitroolefins Catalyzed by Primary Amine Thiourea Organocatalysts

J.-R. Chen*, Y.-Q. Zou, L. Fu, F. Ren, F. Tan, W.-J. Xiao*

Tetrahedron 2010, 66, 5367-5372.

DOI: 10.1016/j.tet.2010.05.056

   
 
10.   Microwave-assisted,palladium-catalyzed carbonylative cyclization —Rapid synthesis of 2-quinolones from unprotected 2-iodoanilines and terminal alkynes

J.-R. Chen*, J. Liao, W.-J. Xiao*

Can. J. Chem. 2010, 88, 331-337.

DOI: 10.1139/v10-002

   
 
9.   Novel Thiourea-Amine Bifunctional Catalysts for Asymmetric Conjugate Addition of Ketones/Aldehydes to Nitroalkenes

J.-R. Chen*, Y.-J. Cao, Y.-Q. Zou, F. Tan, L. Fu, X.-Y. Zhu, W.-J. Xiao*

Org. Biomol. Chem. 2010, 8, 1275-1279.

DOI: 10.1039/b925962g

   
 
8.   Highly Efficient Route to Functionalized Tetrahydrocarbazoles Using a Tandem Cross-Metathesis/Intramolecular-Hydroarylation Sequence

X.-L. An, J.-R. Chen*, C.-F. Li, F.-G. Zhang, Y.-Q. Zou, Y.-C. Guo, W.-J. Xiao*

Chem. Asian J. 2010, 5, 2258-2265.

DOI: 10.1002/asia.201000315

   
 

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

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