84983-99-3

Upstream product

• 2026-48-4 (S)-valinol 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 88241-71-8 (S)-2-{[(S)-(4-Methoxy-phenyl)-phenyl-methyl]-amino}-3-methyl-butan-1-ol 
• 183986-29-0 (S)-(+)-4-Isopropyl-3-(4-methoxybenzyl)oxazolidin-2-one 
• 263757-74-0 (4R,5R)-1,3-Bis-((S)-1-methoxymethyl-2-methyl-propyl)-4,5-bis-(4-methoxy-phenyl)-imidazolidine 
• 228555-33-7 N,N'-bis-(1-methoxymethyl-2-methyl-propyl)-1,2-bis-(4-methoxy-phenyl)-ethane-1,2-diamine 
• 145524-34-1 (S)-2-(4-methoxybenzylamino)-3-methylbutan-1-ol 
• 153827-83-9 ((S)-1-Methoxymethyl-2-methyl-propyl)-[1-(4-methoxy-phenyl)-meth-(E)-ylidene]-amine 

Relevant academic research and scientific papers

Factors influencing the stereoselectivity in the cycloaddition of imino-dienophiles derived from amino ethers, amino alcohols, and amino acid esters

Imino dienophiles derived from amino ethers, amino alcohols and amino esters undergo Lewis acid promoted cycloaddition with Danishefsky's diene. Cyclic chelation between the imine and oxygen atom increases the stereoselectivity of the reaction.