130222-85-4

Basic information

• Product Name: 5-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-D-ribitol
• Synonyms: 5-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-D-ribitol
• CAS NO: 130222-85-4
• Molecular Weight: 430.616
• Mol File: 130222-85-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 5-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-D-ribitol(CAS DataBase Reference)
• NIST Chemistry Reference: 5-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-D-ribitol(130222-85-4)
• EPA Substance Registry System: 5-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-D-ribitol(130222-85-4)

Safety Data

• Hazardous Substances Data: 130222-85-4(Hazardous Substances Data)

Upstream product

• 96690-02-7 5-O-(tert-butyldiphenylsilyl)-2,3-O-isopropylidene-D-ribofuranose 
• 67814-68-0 2,3-O-isopropylidene-β-D-ribofuranose 
• 532-20-7 D-Ribose 

Downstream Products

• 1314971-01-1 1,4-anhydro-5-O-[tert-Butyl(diphenyl)silyl)-2,3-O-(1-methylethylidene)-D-ribitol 
• 491-19-0 1,4-anhydro-D-ribitol 

Relevant articles and documents

Stereoselective synthesis of selenium-containing glycoconjugates via the mitsunobu reaction

A simple and efficient route for the synthesis of new glycoconjugates has been developed. The approach acts as a model for a mini-library of compounds with a deoxy-selenosugar core joined to a polyphenolic moiety with well-known antioxidant properties. An unexpected stereocontrol detected in the Mitsunobu key reaction led to the most attractive product showing a natural Dconfiguration. Thus, we were able to obtain the target molecules from the commercially available D-ribose via a shorter and convenient sequence of reactions.