159108-90-4

Upstream product

• 17226-85-6 α,β-anti-methyl 3-hydroxy-2-methyl-3-(p-methoxyphenyl)propionate 
• 17226-85-6 α,β-syn-methyl 3-hydroxy-2-methyl-3-(p-methoxyphenyl)propionate 
• 17226-85-6 α-methyl-β-hydroxy-β-(p-methoxyphenyl)ethyl propionate 
• 86109-34-4 methyl 3-(4'-methoxyphenyl)-2-methyl-3-oxopropanoate 
• 123-11-5 4-methoxy-benzaldehyde 
• 119018-10-9 (2R,3R)-methyl 3-acetoxy-3-(4-methoxyphenyl)-2-methylpropanoate 

Downstream Products

• 159108-93-7 (+)-(2,3-syn)-3-methoxy-3-(4-methoxyphenyl)-2-methylpropan-1-ol 
• 159108-94-8 (+)-(3,4-syn)-4-methoxy-4-(4-methoxyphenyl)-3-methylbutanenitrile 
• 159108-92-6 (+)-(1,2-syn)-3-(tert-butyldimethylsiloxy)-1-methoxy-1-(4-methoxyphenyl)-2-methylpropane 
• 159108-91-5 (+)-(1,2-syn)-3-(tert-butyldimethylsiloxy)-1-(4-methoxyphenyl)-2-methylpropan-1-ol 

Relevant academic research and scientific papers

Confinement-Controlled, Eithersyn- oranti-Selective Catalytic Asymmetric Mukaiyama Aldolizations of Propionaldehyde Enolsilanes

Protected aldols (i.e., true aldols derived from aldehydes) with eithersyn- oranti- stereochemistry are versatile intermediates in many oligopropionate syntheses. Traditional stereoselective approaches to such aldols typically require several nonstrategic

Formal total syntheses of (-)-oudemansins A, B and X based on a lipase-catalysed hydrolysis of an acetate

A highly stereoselective synthesis of versatile chiral synthons possessing two stereogenic centres and based on the enzyme hydrolysis of an acetate, has been achieved and an application of this to the formal total synthesis of (-)-oudemansins A (1), B (2)

A highly stereoselective synthesis of the versatile chiral synthons possessing two stereogenic centers, the formal total syntheses of (-)- oudemansins A, B, and X

A highly stereoselective synthesis of the versatile chiral synthons possessing two stereogenic centers. (2R,3R)-8 and (2S,3S)-8 was achieved and the application of (2R,3R)-8 into the formal total syntheses of (-)- oudemansins A(2), B(3), and X(4) were des