367910-02-9

Upstream product

• 367909-99-7 (1RS,2S,3R,4R)-3-(tert-butyldiphenylsilyl)oxymethyl-4-methoxymethoxy-4-(3,4-dimethoxyphenyl)-2-methyl-1-(3,4-methylenedioxyphenyl)-1-butanol 
• 367909-94-2 (2S,3R,4R)-3-(tert-butyldiphenylsilyl)oxymethyl-4-(3,4-dimethoxyphenyl)-2-methyl-4-butanolide 
• 367909-91-9 (2S,3R,4R)-4-(3,4-dimethoxyphenyl)-2-methyl-3-pivaloyloxymethyl-4-butanolide 
• 367909-90-8 (3R,4R)-4-(3,4-dimethoxyphenyl)-3-(pivaloyloxymethyl)-4-butanolide 
• 367910-01-8 (2S,3R)-3-[(1R)-1-methoxymethoxy-1-(3,4-dimethoxyphenyl)methyl]-2-methyl-4-butanolide 
• 367909-93-1 (2S,3R)-3-[(1R)-1-hydroxy-1-(3,4-dimethoxyphenyl)methyl]-2-methyl-4-butanolide 
• 367909-92-0 (2S,3R,4R)-3-hydroxymethyl-4-(3,4-dimethoxyphenyl)-2-methyl-4-butanolide 
• 2635-13-4 1,2-(methylenedioxy)-4-bromobenzene 
• 367910-00-7 (1RS,2S,3R)-3-[(1R)-1-methoxymethoxy-1-(3,4-dimethoxyphenyl)methyl]-2-methyl-1-(3,4-methylenedioxyphenyl)-1,4-butanediol 

Relevant academic research and scientific papers

First stereoselective synthesis of (+)-magnostellin C, a tetrahydrofuran type of lignan bearing a chiral secondary benzyl alcohol

(+)-Magnostellin C, which is a tetrahydrofuran type of lignan bearing a chiral secondary benzylic hydroxy group, was stereoselectively synthesized from L-arabinose by using threo selective aldol condensation.