3868-08-4

Upstream product

• 3868-03-9 1,6:2,3-dianhydro-β-D-mannopyranose 
• 98-59-9 p-toluenesulfonyl chloride 
• 88261-50-1 1,6:2,3-dianhydro-4-O-tert-butyldimethylsilyl-β-D-mannopyranose 
• 498-07-7 levoglucosan 
• 3868-05-1 1,6-anhydro-2-O-(4-toluenesulfonyl)-β-D-glucopyranose 

Downstream Products

• 29332-85-2 1,6-anhydro-2,4-dideoxy-2,4-difluoro-β-D-glucopyranoside 
• 359772-64-8 1,6-Anhydro-2-O-benzyl-3,4-dideoxy-3,4-epimino-β-D-altropyranose 
• 856409-33-1 1,6-anhydro-2-deoxy-3-O-mesyl-4-O-tosyl-β-D-arabino-hexopyranose 
• 856409-40-0 1,6-anhydro-4-azido-2,4-dideoxy-3-O-tosyl-β-D-arabino-hexopyranose 
• 856409-34-2 1,6-anhydro-3-azido-2,3-dideoxy-4-O-tosyl-β-D-xylo-hexopyranose 
• 856409-39-7 1,6-anhydro-3-azido-2,3-dideoxy-4-O-tosyl-β-D-arabino-hexopyranose 
• 270088-60-3 1,6-anhydro-2-deoxy-4-O-(p-toluenesulfonyl)-β-D-glucopyranose 

Relevant academic research and scientific papers

Exploring the Chemistry of Non-sticky Sugars: Synthesis of Polyfluorinated Carbohydrate Analogues of d-Allopyranose

There is a growing interest in the preparation of polyfluorinated carbohydrates. A limited number of fluorohexopyranosides have been used in biological investigations because of the synthetic challenge they present. Hence, we report the synthesis of fluor

New chiral building blocks and branched 1,6-anhydro sugars from regio- and stereoisomeric Cerny epoxides

The tandem epoxide→allyl alcohol rearrangement-cuprate cross-coupling previously described for the Cerny epoxide 1, to yield the allyl alcohol 2, was extended to the regioisomeric epoxy-tosylate 3, to yield allyl alcohol 4, and to the stereoisomeric epoxi