textjournal article
Synthesis of Arylphosphonates via Palladium-Catalyzed Coupling Reactions of Aryl Imidazolylsulfonates with H-Phosphonate Diesters
Abstract
A palladium-catalyzed reaction of an aryl imidazolylsulfonate with an H-phosphonate diester in the presence of DPPP and iPr2NEt is described. The reactions proceed efficiently to generate the corresponding arylphosphonates in good to excellent yields. The advantages of this method include good substrate generality, high efficiency, and experimental ease- Text
- Journal contribution
- Biophysics
- Biochemistry
- Microbiology
- Genetics
- Molecular Biology
- Infectious Diseases
- Biological Sciences not elsewhere classified
- Chemical Sciences not elsewhere classified
- arylphosphonate
- presence
- Aryl Imidazolylsulfonates
- iPr 2NEt
- substrate generality
- Arylphosphonate
- method
- Synthesi
- diester
- efficiency
- DPPP
- aryl imidazolylsulfonate
- DiestersA
- yield
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Last time updated on 16/03/2018
This paper was published in The Francis Crick Institute.
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