154367-75-6

Upstream product

• 5707-04-0 Phenylselenyl chloride 
• 134355-03-6 6-deoxy-D-glucal 
• 154367-73-4 acetyl 4-O-acetyl-2-deoxy-2-selenophenyl-3-O-(triethyl)silyl-β-D-fuco-pyranoside 
• 154367-80-3 acetyl 4-O-acetyl-2-deoxy-2-(selenophenyl)-β-D-fuco-pyranoside 
• 154367-72-3 4-O-acetyl-3-O-((triethyl)silyl)-D-fucal 

Downstream Products

• 154367-76-7 2-naphthyl 4-O-acetyl-3-O<3-O-((tert-butyldimethyl)silyl)-2,6-dideoxy-2-iodo-4-O-methyl-α-D-talo-pyranosyl>-2,6-dideoxy-2-(selenophenyl)-β-D-galacto-pyranoside 

Relevant academic research and scientific papers

Studies on the synthesis of aureolic acid antibiotics: Highly stereoselective synthesis of aryl 2-deoxy-β-glycosides via the Mitsunobu reaction and synthesis of the olivomycin A-B disaccharide

The Mitsunobu reaction of phenols and 1,2-cis-2-thiophenyl-α-D-glycopyranoses or 1,2-cis-2-selenophenyl-α-D-glycopyranoses is a very effective method for the highly stereoselective synthesis of aryl 2-deoxy-β-D-glycosides. The equatorial 2-thiophenyl or 2

Synthesis of naphthyl A-B disaccharides corresponding to olivomycin A and mithramycin

Highly stereoselective syntheses of naphthyl disaccharides 4 and 5, which correspond to the A-B dissaccharide units of olivomycin A and mithramycin, are described.