566949-69-7

Upstream product

• 80522-42-5 triisopropylsilyl trifluoromethanesulfonate 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 1259282-24-0 (1S,2S)-2-allyl-1-(3,4-dimethoxyphenyl)-1,3-propanediol 
• 566949-66-4 (4S)-4-benzyl-3-{(2R)-2-[(S)-(hydroxy)(3,4-dimethoxyphenyl)methyl]-4-pentenoyl}-2-oxazolidinone 
• 104266-88-8 (4S)-4-benzyl-3-pent-4-enoyl-1,3-oxazolidin-2-one 
• 13154-24-0 triisopropylsilyl chloride 
• 566949-68-6 (2S)-2-[(S)-(3,4-dimethoxyphenyl)(triisopropylsilyloxy)methyl]-4-penten-1-ol 
• 566949-67-5 (4S)-4-benzyl-3-{(2R)-2-[(S)-(3,4-dimethoxyphenyl)(triisopropylsilyloxy)methyl]-4-pentenoyl}-2-oxazolidinone 

Downstream Products

• 566949-76-6 (E)-(4S,5S)-5-(3,4-dimethoxyphenyl)-1-(4-methoxyphenyl)-5-(triisopropylsilyloxy)-4-(triisopropylsilyloxy)methyl-1-pentene 
• 566949-72-2 (3S,4S)-4-(3,4-dimethoxyphenyl)-4-(triisopropylsilyloxy)-3-(triisopropylsilyloxy)methylbutanal 

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

Syntheses of the stereoisomers of neolignans morinol C and D

Morinol C and morinol D are neolignans isolated from the Chinese medicinal herb Morina chinensis as racemates. (1R,2R)-Morinol C and (1S,2R)-morinol D were synthesized from (+)-(3R,4R)-4-(3,4-dimethoxyphenyl)-3-pivaloyloxymethyl-4-butanolide 4. On the other hand, (1S,2S)-morinol C and (1R,2S)-morinol D were synthesized from anti-aldol product 8.