210286-19-4

Upstream product

• 58479-61-1 tert-butylchlorodiphenylsilane 
• 210286-18-3 (2S,3S,4S,5R)-2-Hydroxymethyl-5-((R)-1-methoxymethoxy-undecyl)-tetrahydro-furan-3,4-diol 
• 3452-09-3 1-nonyne 
• 210286-17-2 (2S,3R,4S,5S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-5-((R)-1-methoxymethoxy-undec-3-ynyl)-tetrahydro-furan 
• 210286-16-1 (R)-1-((2S,3S,4R,5S)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-undec-3-yn-1-ol 
• 210286-14-9 (2S,3R,4S,5S)-3,4-Bis-benzyloxy-2-benzyloxymethyl-5-(R)-oxiranyl-tetrahydro-furan 
• 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.