212757-45-4

Upstream product

• 212757-44-3 (4R,5R)-4-(3,5-dimethoxyphenyl)-5-propyl-1,3-dioxolane-2-thione 
• 38228-29-4 1,3-dimethoxy-5-(pent-1-en-1-yl)benzene 
• 20469-65-2 1-bromo-3,5-dimethoxybenzene 
• 109-67-1 1-penten 
• 212757-42-1 1-(3,5-dimethoxyphenyl)-1,2-pentanediol 

Downstream Products

• 212757-46-5 (R)-1-(2-bromo-3,5-dimethoxyphenyl)-2-pentanol 

Relevant academic research and scientific papers

Asymmetric Total Synthesis of the Complex Polycyclic Xanthone FD-594

A highly convergent approach was developed to achieve the first asymmetric and scalable total synthesis of FD-594, a complex polycyclic xanthone natural product from Streptomyces sp. TA-0256, in a longest linear sequence (LLS) of 20 steps. The trans-9,10-

Synthesis of both enantiomers of hiburipyranone

Both enentiomers of hiburipyranone, a cytotoxic metabolite of marine sponge, was synthesized employing Sharpless' asymmetric dihydroxylation as a key step and absolute configuration of the natural compound at C-3 position was determined to be R.