210286-23-0

Upstream product

• 210286-15-0 (2S,3R,4S,5S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-5-(S)-oxiranyl-tetrahydro-furan 
• 3452-09-3 1-nonyne 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 107-30-2 chloromethyl methyl ether 
• 210286-22-9 (S)-1-((2S,3S,4R,5S)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-undec-3-yn-1-ol 
• 162239-07-8 1-deoxy-1-α-ethenyl-2,3,5-tri-O-benzyl-L-xylose 

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.