1259282-26-2

Upstream product

• 566949-66-4 (4S)-4-benzyl-3-{(2R)-2-[(S)-(hydroxy)(3,4-dimethoxyphenyl)methyl]-4-pentenoyl}-2-oxazolidinone 
• 1259282-24-0 (1S,2S)-2-allyl-1-(3,4-dimethoxyphenyl)-1,3-propanediol 
• 108-24-7 acetic anhydride 

Downstream Products

• 1259282-28-4 (1S,2S)-1-(3,4-dimethoxyphenyl)-2-[(E)-3-(4-methoxyphenyl)-2-propen-1-yl]trimethylene diacetate 
• 1259282-32-0 (Z)-(4S,5S)-5-(3,4-dimethoxyphenyl)-1-(4-methoxyphenyl)-5-(triisopropylsilyloxy)-4-(triisopropylsilyloxy)methyl-1-pentene 
• 566949-76-6 (E)-(4S,5S)-5-(3,4-dimethoxyphenyl)-1-(4-methoxyphenyl)-5-(triisopropylsilyloxy)-4-(triisopropylsilyloxy)methyl-1-pentene 

Relevant academic research and scientific papers

Improved syntheses of morinol C and D by employing mizoroki-heck reaction and their cytotoxic and antimicrobial activities

Improved syntheses of optically pure (-)- and (+)- morinol C, and (-)- and (+)-morinol D were achieved by employing the Mizoroki-Heck reaction to construct the cinnamyl moiety. The protective group of the alkene substrate affected the yield of this key re