Binaphthol-Derived Bisphosphoric Acids Serve as Efficient Organocatalysts for Highly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides to Electron-Deficient Olefins-Reference-Cited by-同舟云学术

Binaphthol-Derived Bisphosphoric Acids Serve as Efficient Organocatalysts for Highly Enantioselective 1,3-Dipolar Cycloaddition of Azomethine Ylides to Electron-Deficient Olefins

Published:2011-08-08 Issue:34 Volume:133 Page:13504-13518
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

He Long¹²,Chen Xiao-Hua¹,Wang De-Nan¹,Luo Shi-Wei¹,Zhang Wen-Quan¹,Yu Jie¹,Ren Lei¹,Gong Liu-Zhu¹

Affiliation:

1. Hefei National Laboratory for Physical Sciences at the Microscale and Department of Chemistry, University of Science and Technology of China, Hefei, 230026, China

2. College of Chemistry and Chemical Engineering, China West Normal University, Nanchong, 637002, China

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja204218h

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4. Intramolecular Dipolar Cycloaddition Reactions of Azomethine Ylides

5. Construction of Enantiopure Pyrrolidine Ring System via Asymmetric [3+2]-Cycloaddition of Azomethine Ylides

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