Palladium‐Catalyzed Desulfitative Cross‐Coupling Reaction of Sodium Arylsulfinates with H‐Phosphonate Diesters

Tao Miao; Lei Wang

doi:10.1002/adsc.201300983

journal article Mar 12, 2014

Palladium‐Catalyzed Desulfitative Cross‐Coupling Reaction of Sodium Arylsulfinates with H‐Phosphonate Diesters

Tao Miao

Lei Wang

Advanced Synthesis & Catalysis Vol. 356 No. 5 pp. 967-971 · Wiley

View at Publisher Save 10.1002/adsc.201300983

Abstract

AbstractA novel and convenient palladium‐catalyzed cross‐coupling reaction of H‐phosphonate diesters with sodium arylsulfinates was developed via desulfitation in the presence of silver carbonate and tetra‐butylammonium chloride. This method is highly efficient and provides a rapid access to a broad spectrum of arylphosphonate diesters in good to excellent yields.magnified image

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Citations

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References

Details

Published: Mar 12, 2014
Vol/Issue: 356(5)
Pages: 967-971
License: View

Authors

The Jack H. Skirball Center for Chemical Biology & Proteomics, The Salk Institute for Biological Studies, La Jolla, California 92037

Cite This Article

Tao Miao, Lei Wang (2014). Palladium‐Catalyzed Desulfitative Cross‐Coupling Reaction of Sodium Arylsulfinates with H‐Phosphonate Diesters. Advanced Synthesis & Catalysis, 356(5), 967-971. https://doi.org/10.1002/adsc.201300983

Palladium‐Catalyzed Desulfitative Cross‐Coupling Reaction of Sodium Arylsulfinates with H‐Phosphonate Diesters

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