(4)-2-[ 2 -( diphénylphosphino) phénol] -4,5 - dihydro - 5,5 - diméthyl- 4 -(1 - méthylethyl)- oxazole,97 %

Code: 719641-500mg D2-231

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Use of 5,5-(Dimethyl)-i-Pr-PHOX as a Practical Equivalent to t-Bu-PHOX in Asymmetric CatalysisDesign, Synthesis, and Applications of Potential Substitutes of t-Bu...


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Votre prix
$254.43 500MG

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Use of 5,5-(Dimethyl)-i-Pr-PHOX as a Practical Equivalent to t-Bu-PHOX in Asymmetric CatalysisDesign, Synthesis, and Applications of Potential Substitutes of t-Bu-Phosphinooxazoline in Pd-Catalyzed Asymmetric Transformations and Their Use for the Improvement of the Enantioselectivity in the Pd-Catalyzed Allylation Reaction of Fluorinated Allyl Enol Carbonates

(S)-5,5-(Dimethyl)-i-Pr-PHOX is a phosphinooxazoline ligand (PHOX), belongs to the class of non-C2 symmetric chiral ligand. It can be used in: The enantioselective Pd-catalyzed allylation reactions. The synthesis of (R)-2-phenyl-2,5-dihydrofuran by the enantioselective Heck reaction between 2,3-dihydrofuran and phenyl triflate. The allylation reaction of fluorinated allyl enol carbonates and fluorinated silyl enol ethers to prepare allylated tert α-fluoroketones.

Packaging

500 mg in glass bottle

assay97%
formsolid
InChI keyJGUZEKBWCGNHHN-DEOSSOPVSA-N
InChI1S/C26H28NOP/c1-19(2)24-26(3,4)28-25(27-24)22-17-11-12-18-23(22)29(20-13-7-5-8-14-20)21-15-9-6-10-16-21/h5-19,24H,1-4H3/t24-/m0/s1
mp124-128 °C
Quality Level100
SMILES stringCC(C)[C@@H]1N=C(OC1(C)C)c2ccccc2P(c3ccccc3)c4ccccc4
Cas Number1152313-76-2
Hazard Class6.1
Un Number2811
Pack GroupIII
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