182816-77-9

Upstream product

• 136152-94-8 1-β-formyl-3-α-hydroxy-3-β-allyl-4α,5α-O-isopropylidene-tetrahydrofuran 
• 622-30-0 N-benzyl hydroxylalmine 
• 175877-45-9 3-C-allyl-1,2:5,6-di-O-isopropylidene-α-D-allofuranose 
• 156343-31-6 1',2'-O-isopropylidene-3'-C-(prop-1-enyl)-α-D-allyl-1',4'-furanose 
• 2847-00-9 1,2:5,6-di-O-isopropylidene-α-D-hexofuran-3-ulose 

Downstream Products

• 773895-20-8 (2'aR,3aS,5'R,5'aR,6S,6aR)-1,1'-dibenzyl-5'-hydroxy-spiro[tetrahydrofurano[3,4-c]isoxazole-6,4'-cyclopent[c]isoxazole] 
• 773895-22-0 (2'aR,3aR,5'R,5'aS,6S,6aS)-1,1'-dibenzyl-5'-hydroxy-spiro[tetrahydrofurano[3,4-c]isoxazole-6,4'-cyclopent[c]isoxazole] 
• 773895-16-2 (1S,2R,3R,5R)-3-Allyloxy-7-benzyl-2-hydroxy-6-oxa-7-aza-bicyclo[3.2.1]octane-3-carbaldehyde 

Relevant academic research and scientific papers

A simple route to optically active, functionalized five-, six- and seven-membered carbocyclic derivatives

The isoxazolidinocarbocyclic derivatives 6, 7 and 13, useful as precursors for unnatural bioactive chiral carbocyclic nucleosides and for glycosidase inhibitors have been synthesized from D-glucose through intramolecular 1,3-dipolar cycloaddition.