CataCXium F sulf
Appearance
Names | |
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IUPAC name
(±)-Dicyclohexyl-{9-[3-(4-sulfonylphenyl)propyl]-2-sulfonylfluoren-9-yl}phosphonium hydrogensulfate
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Other names
CataCXium F sulf
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.221.684 |
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C34H43O10PS3 | |
Molar mass | 738.87 g/mol |
Appearance | pale yellow solid |
Solubility | soluble in water |
Hazards | |
GHS labelling: | |
Warning | |
H315, H319, H335 | |
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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CataCXium F sulf is a water-soluble organophosphorus compound derived from fluorene. The palladium complexes of the respective phosphine[clarification needed] show an excellent activity in various palladium-catalyzed coupling reactions, including Suzuki reactions, Sonogashira couplings and Buchwald–Hartwig reactions.
References
[edit]- C.A. Fleckenstein; H. Plenio, Highly efficient Suzuki-Miyaura coupling of heterocyclic substrates through rational reaction design. Chemistry-A European Journal 2008, 14(14), 4267–4279.
- C.A. Fleckenstein; H. Plenio, Aqueous/organic cross coupling: Sustainable protocol for Sonogashira reactions of heterocycles. Green Chemistry 2008, 10, 563–570. doi:10.1039/B800154E
- C.A. Fleckenstein; H. Plenio, Efficient Suzuki-Miyaura Coupling of (Hetero)aryl Chlorides with Thiophene- and Furanboronic Acids in Aqueous n-Butanol. Journal of Organic Chemistry 2008, 73, 3236–3244.
- C.A Fleckenstein; R. Kadyrov; H. Plenio, Efficient Large-Scale Synthesis of 9-Alkylfluorenyl Phosphines for Pd-Catalyzed Cross-Coupling Reactions. Organic Process Research & Development 2008, 12, 475–479.
- C.A. Fleckenstein; H. Plenio, Aqueous cross-coupling. Highly efficient Suzuki–Miyaura coupling of N-heteroaryl halides and N-heteroarylboronic acids. Green Chemistry 2007, 9, 1287–1291. doi:10.1039/B711965H