159108-91-5

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 159108-90-4 (+)-(2,3-syn)-3-(4-methoxyphenyl)-2-methylpropane-1,3-diol 
• 123-11-5 4-methoxy-benzaldehyde 
• 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 
• 119018-10-9 (2R,3R)-methyl 3-acetoxy-3-(4-methoxyphenyl)-2-methylpropanoate 
• 86109-34-4 methyl 3-(4'-methoxyphenyl)-2-methyl-3-oxopropanoate 

Downstream Products

• 159108-92-6 (+)-(1,2-syn)-3-(tert-butyldimethylsiloxy)-1-methoxy-1-(4-methoxyphenyl)-2-methylpropane 
• 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 

Relevant academic research and scientific papers

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