367909-83-9

Upstream product

• 107-30-2 chloromethyl methyl ether 
• 367909-82-8 (2R,3R,4S)-3-hydroxy-2-[(1R)-1-hydroxy-1-(3,4-dimethoxyphenyl)methyl]-5-trityloxy-4-pentanolide 
• 326606-31-9 (3R,4S)-3-hydroxy-5-trityloxy-4-pentanolide 
• 120-14-9 3,4-dimethoxy-benzaldehyde 

Downstream Products

• 367909-84-0 (2S,3R,4R,5R)-3,5-bis(methoxymethoxy)-5-(3,4-dimethoxyphenyl)-4-pivaloyloxymethyl-1-trityloxy-2-pentanol 
• 367909-85-1 (2S,3R,4R,5R)-3,5-bis(methoxymethoxy)-5-(3,4-dimethoxyphenyl)-4-pivaloyloxymethyl-1,2-pentanediol 
• 367909-89-5 (2S,3R,4R)-4-(3,4-dimethoxyphenyl)-2-phenoxythiocarbonyloxy-3-pivaloyloxymethyl-4-butanolide 
• 367909-86-2 (2R,3R,4R)-2,4-bis(methoxymethoxy)-4-(3,4-dimethoxyphenyl)-3-pivaloyloxymethylbutanal 
• 367909-81-7 (2R,3S,4R,5R)-2-hydroxy-3-methoxymethoxy-5-(3,4-dimethoxyphenyl)-4-pivaloyloxymethyltetrahydrofuran 
• 367909-87-3 (2S,3R,4R)-2-methoxymethoxy-4-(3,4-dimethoxyphenyl)-3-pivaloyloxymethyl-4-butanolide 
• 367909-88-4 (2S,3S,4R)-2-hydroxy-4-(3,4-dimethoxyphenyl)-3-pivaloyloxymethyl-4-butanolide 

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.