(S)-4-((S)-sec-Butyl)-2-(pyridin-2-ylmethyl)-4,5-dihydrooxazole

97%

Reagent Code: #237862
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CAS Number 217653-28-6

science Other reagents with same CAS 217653-28-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.29 g/mol
Formula C₁₃H₁₈N₂O
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. Its oxazoline-pyridine framework coordinates effectively with transition metals like copper or nickel, enabling high stereoselectivity in transformations such as cyclopropanations and aldol reactions. Commonly employed in pharmaceutical intermediates synthesis where precise stereochemistry is critical. Also applied in the development of chiral ligands for catalytic asymmetric hydrogenation and conjugate addition reactions. Its rigid structure and tunable steric environment make it valuable in optimizing enantioselectivity across various organic transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,200.00
(S)-4-((S)-sec-Butyl)-2-(pyridin-2-ylmethyl)-4,5-dihydrooxazole
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Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. Its oxazoline-pyridine framework coordinates effectively with transition metals like copper or nickel, enabling high stereoselectivity in transformations such as cyclopropanations and aldol reactions. Commonly employed in pharmaceutical intermediates synthesis where precise stereochemistry is critical. Also applied in the development of chiral ligands for catalytic asymmetric hydrogen

Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. Its oxazoline-pyridine framework coordinates effectively with transition metals like copper or nickel, enabling high stereoselectivity in transformations such as cyclopropanations and aldol reactions. Commonly employed in pharmaceutical intermediates synthesis where precise stereochemistry is critical. Also applied in the development of chiral ligands for catalytic asymmetric hydrogenation and conjugate addition reactions. Its rigid structure and tunable steric environment make it valuable in optimizing enantioselectivity across various organic transformations.

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