90301-25-0

Upstream product

• 40245-97-4 O⁴-(toluene-4-sulfonyl)-1,6-anhydro-β-D-mannopyranose 
• 98-59-9 p-toluenesulfonyl chloride 
• 3868-04-0 1,6:3,4-dianhydro-β-D-altropyranose 
• 5349-02-0 1,6-Anhydro-2,3-O-isopropylidene-4-O-p-toluenesulfonyl-β-D-mannopyranose 
• 34147-09-6 1,6:3,4-dianhydro-β-D-talopyranose 

Downstream Products

• 90301-26-1 -1,6-anhydro-3-deoxy-2-O-p-toluenesulfonyl-β-D-arabino-hexopyranose 
• 58394-31-3 1,6-anhydro-2,3-dideoxy-β-D-erythro-hex-2-enopyranose 
• 872050-03-8 1,6-anhydro-4-deoxy-4-methyl-2-O-p-tolylsulfonyl-β-D-idopyranose 
• 872050-01-6 1,6-anhydro-4-deoxy-4-methyl-2-O-p-tolylsulfonyl-β-D-lyxopyranos-3-ulose 

Relevant academic research and scientific papers

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