(R)-2-([2, 2'-Bipyridin]-6-yl)-4-phenyl-4, 5-dihydrooxazole
98%, 99%e.e.
- Product Code: 231100
CAS:
1666123-70-1
| Molecular Weight: | 301.34 g./mol | Molecular Formula: | C₁₉H₁₅N₃O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD34563663 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transition metal-catalyzed reactions. It plays a key role in promoting stereoselectivity in carbon-carbon bond-forming reactions, such as allylic alkylation and Heck-type reactions. Its rigid oxazoline-bipyridine framework enhances metal coordination control, leading to high enantiomeric excess in the synthesis of pharmaceutical intermediates and fine chemicals. Commonly employed with palladium, nickel, or copper complexes to achieve efficient asymmetric induction under mild reaction conditions.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft90,160.97 |
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| 0.250 | 10-20 days | Ft135,031.28 |
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| 1.000 | 10-20 days | Ft337,525.66 |
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(R)-2-([2, 2'-Bipyridin]-6-yl)-4-phenyl-4, 5-dihydrooxazole
Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transition metal-catalyzed reactions. It plays a key role in promoting stereoselectivity in carbon-carbon bond-forming reactions, such as allylic alkylation and Heck-type reactions. Its rigid oxazoline-bipyridine framework enhances metal coordination control, leading to high enantiomeric excess in the synthesis of pharmaceutical intermediates and fine chemicals. Commonly employed with palladium, nickel, or copper complexes to achieve efficient asymmetric induction under mild reaction conditions.
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