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(4S)-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro-5,5-dimethyl-4-(1-methylethyl)-oxazole

ALDRICH/719641 - 97%

Synonym: (S)-2-(2-(Diphenylphosphino)phenyl)-4-isopropyl-5,5-dimethyl-4,5-dihydrooxazole; (S)-5,5-(Dimethyl)-i-Pr-PHOX

CAS Number: 1152313-76-2
Empirical Formula (Hill Notation): C26H28NOP
Molecular Weight: 401.48
MDL Number: MFCD16621462
Linear Formula: C26H28NOP
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-719641-500MG 500 mg
$233.00
1/EA
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assay 97%
form solid
InChI 1S/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
InChI key JGUZEKBWCGNHHN-DEOSSOPVSA-N
mp 124-128 °C
SMILES string CC(C)[C@@H]1N=C(OC1(C)C)c2ccccc2P(c3ccccc3)c4ccccc4
Application: (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.

Application: Use of 5,5-(Dimethyl)-i-Pr-PHOX as a Practical Equivalent to t-Bu-PHOX in Asymmetric Catalysis 

Design, 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 
Packaging: 500 mg in glass bottle
Purity 97%
mp 124-128 °C
UNSPSC 12352005

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