210286-12-7

Upstream product

• 210286-11-6 ((2S,3R,4S,5R)-3,4-Bis-benzyloxy-5-dimethoxymethyl-tetrahydro-furan-2-ylmethoxy)-tert-butyl-diphenyl-silane 
• 100-39-0 benzyl bromide 
• 210286-09-2 (2R,3S,4S,5S)-3-benzyloxy-4-hydroxy-5-hydroxymethyl-2-dimethoxymethyl-tetrahydrofuran 
• 210286-10-5 (2S,3R,4S,5R)-4-Benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-dimethoxymethyl-tetrahydro-furan-3-ol 

Relevant academic research and scientific papers

Annonaceous acetogenins: Preparation of new methoxy substituted THF synthons from D-glucose

In connection with the synthesis of cytotoxic annonaceous acetogenin analogs, enantiomerically pure threo (and erythro)-trans THF synthons have been prepared from D-glucose. These synthons are characterized by the presence of two methoxy (or hydroxy) groups in the THF ring, each in a cis configuration with respect to the vicinal side chain.