l-Phenylalanine potassium catalyzed asymmetric formal [3 + 3] annulation of 2-enoyl-pyridine N-oxides with acetone

Literature Information

Publication Date 2017-10-09
DOI 10.1039/C7QO00796E
Impact Factor 5.281
Authors

Youguo Xu, Sheng Zhang, Lijun Li, Yukang Wang, Zhenggen Zha, Zhiyong Wang


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Abstract

A highly enantioselective formal [3 + 3] annulation of 2-enoyl-pyridine N-oxides with acetone was developed. In this transformation, an amino-acid salt L-phenylalanine potassium proved to be a robust organocatalyst, and the corresponding annulation derivatives can be obtained with moderate to excellent yields (up to 99%) and good to excellent enantioselectivities (up to 94%).

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