167901-94-2

Upstream product

• 167901-78-2 2,2,2-trifluoroethyl 4-O-benzyl-2,3,6,7,8,9-hexadeoxy-α-D-erythro-non-8-enopyranoside 
• 167901-80-6 tert-butyl 4-O-benzyl-2,3,6,7,8,9-hexadeoxy-α-D-erythro-non-8-enopyranoside 

Downstream Products

• 429618-10-0 2-{(S)-3-(benzyloxy)-3-[(2R,5S)-5-(iodomethyl)tetrahydrofuran-2-yl]propyl}-1,3-dioxolane 
• 429618-11-1 [(2S,5R)-5-((S)-1-Benzyloxy-3-[1,3]dioxolan-2-yl-propyl)-tetrahydro-furan-2-yl]-acetonitrile 

Relevant academic research and scientific papers

Pyranoside alkene templates for the synthesis of CIS-2,5-disubstituted tetrahydrofuran subunits of the acetogenins

The iodoetherification reaction of t-butyl and trityl glycosides of C6 allylated-2,3-dideoxy-D-erythro- and D-threo-pyranosides was examined as part of a model study aimed at the synthesis of the 2,5-disubstituted tetrahydrofuran subunits found in the ace

cis-2,5-Disubstituted Tetrahydrofurans from Pyranosides: A Novel Example of Remote Stereocontrol by the Aglycone

A stereoselective methodology, based on neighboring group participation by the acetal ring oxygen, is described for the preparation of highly functionalizable cis-2,3-disubstituted tetrahydrofurans from C6 alkenyl branched pyranosides.