(4S,4’S,5R,5’R)-2,2’-(Cyclobutane-1,1-diyl)Bis(4,5-Diphenyl-4,5-Dihydrooxazole)

97%

Reagent Code: #237408
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CAS Number 2757082-11-2

science Other reagents with same CAS 2757082-11-2

blur_circular Chemical Specifications

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Weight 498.61 g/mol
Formula C₃₄H₃₀N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid cyclobutane core and oxazoline rings provide a well-defined chiral environment, making it effective in copper-catalyzed cyclopropanation, Diels-Alder, and aldol reactions. Commonly employed in the synthesis of optically active compounds for pharmaceuticals and fine chemicals. Shows high enantioselectivity with various substrates due to its steric and electronic tuning. Also utilized in coordination chemistry with transition metals to form catalysts for stereoselective synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,080.00
inventory 250mg
10-20 days ฿14,350.00
inventory 1g
10-20 days ฿43,020.00

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(4S,4’S,5R,5’R)-2,2’-(Cyclobutane-1,1-diyl)Bis(4,5-Diphenyl-4,5-Dihydrooxazole)
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid cyclobutane core and oxazoline rings provide a well-defined chiral environment, making it effective in copper-catalyzed cyclopropanation, Diels-Alder, and aldol reactions. Commonly employed in the synthesis of optically active compounds for pharmaceuticals and fine chemicals. Shows high enantioselectivity with various substrates due to its steric and electronic tuning. Also utilized in coo

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid cyclobutane core and oxazoline rings provide a well-defined chiral environment, making it effective in copper-catalyzed cyclopropanation, Diels-Alder, and aldol reactions. Commonly employed in the synthesis of optically active compounds for pharmaceuticals and fine chemicals. Shows high enantioselectivity with various substrates due to its steric and electronic tuning. Also utilized in coordination chemistry with transition metals to form catalysts for stereoselective synthesis.

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