6,6'-Bis((R)-4-benzyl-4,5-dihydrooxazol-2-yl)-2,2'-bipyridine

98%, 99%e.e.

Reagent Code: #154658
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CAS Number 2757082-74-7

science Other reagents with same CAS 2757082-74-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 474.55 g/mol
Formula C₃₀H₂₆N₄O₂
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transition metal-catalyzed reactions. It plays a key role in promoting high stereocontrol in carbon-carbon bond-forming reactions such as conjugate additions and cycloadditions. Its rigid bipyridine backbone combined with oxazoline moieties enhances metal coordination and stereoselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly employed with copper, nickel, or palladium complexes to achieve efficient asymmetric induction under mild reaction conditions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,870.00
inventory 1g
10-20 days ฿44,860.00

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6,6'-Bis((R)-4-benzyl-4,5-dihydrooxazol-2-yl)-2,2'-bipyridine
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transition metal-catalyzed reactions. It plays a key role in promoting high stereocontrol in carbon-carbon bond-forming reactions such as conjugate additions and cycloadditions. Its rigid bipyridine backbone combined with oxazoline moieties enhances metal coordination and stereoselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly employed with copper, nickel, or p

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transition metal-catalyzed reactions. It plays a key role in promoting high stereocontrol in carbon-carbon bond-forming reactions such as conjugate additions and cycloadditions. Its rigid bipyridine backbone combined with oxazoline moieties enhances metal coordination and stereoselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly employed with copper, nickel, or palladium complexes to achieve efficient asymmetric induction under mild reaction conditions.

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