(4R,4'R)-2,2'-(1-Phenylpropane-2,2-diyl)bis(4-methyl-4,5-dihydrooxazole)

97%

Reagent Code: #232166
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CAS Number 2757082-30-5

science Other reagents with same CAS 2757082-30-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.36 g/mol
Formula C₁₇H₂₂N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

This chiral bis(oxazoline) ligand is widely used in asymmetric catalysis to enable the formation of enantiomerically enriched compounds. Its rigid bidentate structure and stereochemical stability provide excellent control over the stereochemistry in metal-catalyzed reactions, such as allylic alkylations, aldol additions, and Diels-Alder cyclizations. It is commonly employed in the pharmaceutical industry for the synthesis of optically active drugs and intermediates. The oxazoline rings coordinate effectively with transition metal centers (e.g., copper or palladium), enhancing catalytic efficiency and enantioselectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,610.00
(4R,4'R)-2,2'-(1-Phenylpropane-2,2-diyl)bis(4-methyl-4,5-dihydrooxazole)
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This chiral bis(oxazoline) ligand is widely used in asymmetric catalysis to enable the formation of enantiomerically enriched compounds. Its rigid bidentate structure and stereochemical stability provide excellent control over the stereochemistry in metal-catalyzed reactions, such as allylic alkylations, aldol additions, and Diels-Alder cyclizations. It is commonly employed in the pharmaceutical industry for the synthesis of optically active drugs and intermediates. The oxazoline rings coordinate effecti

This chiral bis(oxazoline) ligand is widely used in asymmetric catalysis to enable the formation of enantiomerically enriched compounds. Its rigid bidentate structure and stereochemical stability provide excellent control over the stereochemistry in metal-catalyzed reactions, such as allylic alkylations, aldol additions, and Diels-Alder cyclizations. It is commonly employed in the pharmaceutical industry for the synthesis of optically active drugs and intermediates. The oxazoline rings coordinate effectively with transition metal centers (e.g., copper or palladium), enhancing catalytic efficiency and enantioselectivity.

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