| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6506201 | Chinese Journal of Catalysis | 2016 | 6 Pages |
Abstract
Copper catalyzed asymmetric formal [3+2] cycloaddition of propargylic esters with β-keto phosphonates for the synthesis of chiral phosphonylated 2,3-dihydrofurans was developed. By using a bulky and structurally rigid tridentate ketamine P,N,N ligand, a series of optically active phosphonylated 2,3-dihydrofurans were prepared in high yields and up to 92% ee.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
Xiushuai Chen, Chuanjin Hou, Qing Li, Yanjun Liu, Ruifeng Yang, Xiangping Hu,
![First Page Preview: Enantioselective synthesis of chiral phosphonylated 2,3-dihydrofurans by copper catalyzed asymmetric formal [3+2] cycloaddition of propargylic esters with β-keto phosphonates Enantioselective synthesis of chiral phosphonylated 2,3-dihydrofurans by copper catalyzed asymmetric formal [3+2] cycloaddition of propargylic esters with β-keto phosphonates](/preview/png/6506201.png)