155906-85-7

Upstream product

• 626-19-7 Isophthalaldehyde 
• 161832-74-2 (-)-(S)-2-amino-4-methyl-1,1-diphenylpentanol 
• 100-58-3 phenylmagnesium bromide 
• 7517-19-3 methyl (L)-leucinate hydrochloride 
• 155906-83-5 (S)-2-{[1-(3-{[(E)-(S)-1-(Hydroxy-diphenyl-methyl)-3-methyl-butylimino]-methyl}-phenyl)-meth-(E)-ylidene]-amino}-4-methyl-1,1-diphenyl-pentan-1-ol 

Relevant academic research and scientific papers

Easy preparation of enantiopure C2-symmetrical aminoalcohols derived from m-xylylene diamine

The title compounds were prepared by condensation of isophthaldehyde with chiral amino alcohols or α-amino esters in three different ways depending on the substitution pattern. These methods are: for N-substituted amino alcohols, by reduction of the epime