164118-40-5

Upstream product

• 164118-37-0 (2S,3R)-1-<(4-Methoxyphenyl)methoxy>-3-methyl-4-phenylbutan-2-ol 
• 78571-81-0 2-Hydroxymethyl-3-phenylmethyloxirane 
• 219607-73-5 (2R,3R)-2-(methanesulfonyl)oxy-3-methyl-4-phenyl-1-butanol 
• 219607-74-6 (2S,3R)-1,2-epoxy-3-methyl-4-phenylbutane 
• 164118-39-2 (2S,3R)-2-<(4-Methoxyphenyl)methoxy>-3-methyl-4-phenylbutan-2-ol 

Downstream Products

• 164118-42-7 <2(4S,5R)>-2-<4-<(4-Methoxyphenyl)methoxy>-5-methyl-3-oxo-6-phenylhexyl>-1,3-dioxolane 
• 164118-44-9 <2(4S,5R)>-2-<4-<(4-Methoxyphenyl)methoxy>-5-methyl-3-methylene-6-phenylhexyl>-1,3-dithiane 
• 164118-43-8 <2(4S,5R)>-2-<4-<(4-Methoxyphenyl)methoxy>-5-methyl-3-methylene-6-phenylhexyl>-1,3-dioxolane 
• 644981-59-9 (3R,4R)-4-methyl-5-phenyl-1-penten-3-yl acetate 
• 925453-63-0 (3R,4R)-4-methyl-5-phenyl-1-penten-3-ol 

Relevant academic research and scientific papers

Total Synthesis of the Squalene Synthase Inhibitor Zaragozic Acid C by a Carbonyl Ylide Cycloaddition Strategy

Ketal isomers avoided. The unique 2,8-dioxabicyclo[3.2.1 ]octane core of zaragozic acid C (1) was constructed in a Rh-catalyzed 1,3-dipolar cycloaddition of an alkyne to an ester carbonyl ylide. Another feature of this improved synthesis is the constructi

Synthesis of Zaragozic Acid A/Squalestatin S1

A novel synthetic approach to the construction of the zaragozic acids, which was used for the asymmetric synthesis of zaragozic acid A/squalestatin S1 (1), is described.Fragment 5, representing the tricarboxylic acid core portion, is assembled in three ke