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43158 Aldrich

(R)-(−)-2-[2-(Diphenylphosphino)phenyl]-4-phenyl-2-oxazoline

≥97.0% (31P-NMR)

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Properties

Related Categories Asymmetric Synthesis, Chemical Synthesis, Chiral Catalysts, Ligands, and Reagents, PHOX, Privileged Ligands and Complexes More...
InChI Key   OKUTYUNUKKPYJS-VWLOTQADSA-N
assay   ≥97.0% (31P-NMR)
optical activity   [α]20/D −29.5±3°, c = 1% in chloroform

Description

Other Notes

Chiral ligand employed in enantioselective Pd-catalyzed allylic substitution reactions

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Price and Availability

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Articles

PHOX

Of the thousands of chiral ligands used in asymmetric synthesis a relatively large number exhibit C2-symmetry. More recently, non-symmetrical modular P,N-ligands have been introduced independently by...
William Sommer and Daniel Weibel
Chemfiles Volume 8 Article 2
Keywords: Alkylations, Asymmetric synthesis, Catalysis, Desymmetrizations, Heck Reaction, Hydrogenations, Ligands, Pauson-Khand Reaction, Reductions, transformation

Pfaltz Group - Professor Product Portal

From our library of Articles, Sigma-Aldrich presents Pfaltz Group - Professor Product Portal
Keywords: Asymmetric catalysis, Asymmetric synthesis, Catalysis, Hydrogenations, Ligands

Peer-Reviewed Papers
15

References

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