1802928-40-0

Usage

Uses

Used in Pharmaceutical Industry:
(S)-4-isopropyl-2-(quinolin-2-yl)-4,5-dihydrooxazole is used as a pharmaceutical compound for its potential biological activity. (S)-4-isopropyl-2-(quinolin-2-yl)-4,5-dihydrooxazole's structural diversity and complex nature allow it to interact with various biological targets, making it a valuable asset in the development of new drugs and therapies.
Used in Materials Science:
In the field of materials science, (S)-4-isopropyl-2-(quinolin-2-yl)-4,5-dihydrooxazole is utilized for its unique structural properties. Its potential applications include the development of novel materials with specific characteristics, such as improved stability, reactivity, or selectivity, which can be beneficial in various industrial processes.
Used in Chemical Synthesis:
(S)-4-isopropyl-2-(quinolin-2-yl)-4,5-dihydrooxazole serves as a key intermediate in the synthesis of more complex molecules. Its unique structure allows for further functionalization and modification, making it a valuable building block in the creation of new compounds with diverse applications.
Used in Research and Development:
Due to its structural complexity and potential biological activity, (S)-4-isopropyl-2-(quinolin-2-yl)-4,5-dihydrooxazole is employed as a research compound. It is used to study the effects of structural modifications on the compound's properties and to explore its potential applications in various fields, including pharmaceuticals, materials science, and chemical synthesis.

Upstream product

• 1436-43-7 quinoline-2-carbonitrile 
• 2026-48-4 (S)-valinol 
• 50342-01-3 quinolin-2-ylcarbonyl chloride 
• 93-10-7 quinoline-2-carboxylic acid 

Relevant academic research and scientific papers

Pyridine-oxazoline and quinoline-oxazoline ligated cobalt complexes: Synthesis, characterization, and 1,3-butadiene polymerization behaviors

A series of cobalt complexes supported by pyridine-oxazoline (Pyox) and quinoline-oxazoline (Quox) were synthesized. Determined by single crystal X-ray crystallography, complexes 6a and 7c adopted distorted octahedron and trigonal bipyramid geometries, re

Efficacious and rapid metal- and solvent-free synthesis of enantiopure oxazolines

A rapid and efficient synthesis of oxazolines was performed starting from various nitriles using microwave irradiation combined to metal- and solvent-free conditions to afford high to quantitative yields of the targeted heterocycles.

Pd-catalyzed asymmetric aza-Wacker-type cyclization reaction of olefinic tosylamides

The Pd-catalyzed asymmetric aza-Wacker-type cyclization reaction of the olefinic tosylamides with molecular oxygen as the green oxidant was developed. Under the optimized conditions, excellent catalytic activity and good enantioselectivity with up to 74%

Palladium(II)-catalyzed enantioselective aerobic dialkoxylation of 2-propenyl phenols: A pronounced effect of copper additives on enantioselectivity

A direct O2-coupled Pd(II)-catalyzed enantioselective dialkoxylation of 2-propenylphenols has been developed by utilizing chiral quinoline oxazoline ligands. A detrimental effect of added copper salts on enantioselectivity was observed which is attributed to the displacement of the chiral ligand off of Pd(II). Copyright

Steric effects of the ligand in the enantioselective palladium-catalyzed allylic alkylation using chiral oxazolinylpyridines

Eight new chiral oxazolinylpyridines were prepared and assessed in the enantioselective palladium-catalyzed allylic substitution of 1,3- diphenylprop-2-enyl acetate with dimethyl malonate. Catalytic activity and enantioselectivity were found to be highly