945853-13-4

Upstream product

• 926622-72-2 (R)-ethyl 4-(hydroxy-((S)-1-(2,4,6-triisopropylphenyl)ethyl)amino)-6-methylheptanoate 
• 108-24-7 acetic anhydride 
• 926622-60-8 2-(1-azido-ethyl)-1,3,5-triisopropyl-benzene 
• 926622-53-9 (S)-1-(2,4,6-triisopropylphenyl)ethylamine 
• 926622-58-4 (S)-N-[1-(2,4,6-triisopropylphenyl)ethyl]hydroxylamine 
• 926622-54-0 (S)-[1-(2,4,6-triisopropylphenyl)ethylamino]acetonitrile 
• 926622-56-2 (S,Z)-N-(cyanomethylidene)-1-(2,4,6-triisopropylphenyl)ethanamine N-oxide 
• 926622-65-3 (S,Z)-N-(3-methylbutylidene)-1-(2,4,6-triisopropylphenyl)ethanamine N-oxide 
• 926622-51-7 [(S)-1-(2,4,6-Triisopropyl-phenyl)-ethyl]-carbamic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 
• 102225-88-7 (+/-)-1-(2,4,6-triisopropylphenyl)ethanol 
• 590-86-3 isovaleraldehyde 

Relevant academic research and scientific papers

1-(2,4,6-Triisopropylphenyl)ethylamine: A new chiral auxiliary for the asymmetric synthesis of γ-amino acid derivatives

The title compound has proven to be an excellent chiral auxiliary for nitrones in SmI2-mediated reductive coupling with α,β-unsaturated esters. A variety of such nitrones, prepared from aldehydes and enantiopure N-hydroxy-1-(2,4,6-triisopropylp