1340477-06-6

Upstream product

• 7533-40-6 2-amino-4-methyl-1-pentanol 
• 6630-33-7 ortho-bromobenzaldehyde 
• 2042-37-7 o-cyanobromobenzene 

Downstream Products

• 1340476-86-9 (4R)-4,5-dihydro-2-{2'-[(R)-1-(1-naphthyl)ethylamino]phenyl}-4-isobutyloxazole 
• 1340476-95-0 (4R)-4,5-dihydro-2-[2'-(2,6-diisopropylanilino)phenyl]-4-isobutyloxazole 
• 1340476-82-5 (4R)-4,5-dihydro-2-{2'-[(R)-α-methylbenzylamino]phenyl}-4-isobutyloxazole 
• 1340477-00-0 (4R)-4,5-dihydro-2-[2'-(benzamido)phenyl]-4-isobutyloxazole 
• 1340476-90-5 (4R)-4,5-dihydro-2-[2'-(2,6-dimethylanilino)phenyl]-4-isobutyloxazole 
• 1340477-04-4 (4R)-4,5-dihydro-2-{2'-[(S)-tert-butylsulfinamido]phenyl}-4-isobutyloxazole 
• 1609167-93-2 (4R)-4,5-dihydro-2-(2′-anilinophenyl)-4-isobutyloxazole 

Relevant academic research and scientific papers

Ring-opening polymerization of rac-lactide with aluminum chiral anilido-oxazolinate complexes

A series of dimethylaluminum complexes (L1a-i)AlMe2 (2a-i, where HL1a-i = 2-(2′-ArNH)phenyl-4-R1- oxazoline) bearing chiral, bidentate anilido-oxazolinate ligands have been prepared and characterized. Six of the

Modular synthesis of chiral β-diketiminato-type ligands containing 2-oxazoline moiety via palladium-catalyzed amination

A family of new chiral β-diketiminato-type ligands containing oxazoline moiety has been synthesized in moderate to high yields (typically 30-95%) via a Pd-catalyzed amination reaction of chiral oxazolines with primary amines and amides. Notably, (S)-tert-