112473-47-9

Upstream product

• 102562-01-6 (1R,4S,5S,6S,8R,9R)-4,5-epoxy-8,9-isopropylidenedioxy-7-oxabicyclo<4.3.0>nonan-3-one 
• 102562-02-7 (1R,3R,4R,5S,6S,8R,9R)-4,5-epoxy-8,9-isopropylidenedioxy-7-oxabicyclo<4.3.0>nonan-3-ol 
• 102562-02-7 (1R,3S,4R,5S,6S,8R,9R)-4,5-epoxy-8,9-isopropylidenedioxy-7-oxabicyclo<4.3.0>nonan-3-ol 
• 102562-06-1 (1R,3R,4S,5S,6S,8R,9R)-3,4,5-tris(benzyloxy)-8,9-isopropylidenedioxy-7-oxabicyclo<4.3.0>nonane 
• 102562-07-2 (3R,3aS,5R,6S,7S,7aS)-5,6,7-Tris-benzyloxy-octahydro-benzofuran-2,3-diol 
• 102562-04-9 (1R,3R,4S,5S,6S,8R,9R)-3,4,5-trihydroxy-8,9-isopropylidenedioxy-7-oxabicyclo<4.3.0>nonane 
• 100-39-0 benzyl bromide 

Downstream Products

• 112473-48-0 (3S,4S,5R)-3,4,5-Tris-benzyloxy-cyclohex-1-enecarbaldehyde 
• 90695-22-0 (1R)-(+)-(1,3,5/2,4)-2,3,4,5-tetrahydroxycyclohexane-1-methanol penta-acetate 
• 102629-12-9 (1R,2S,3S,4S,5S)-5-(acetoxymethyl)cyclohexane-1,2,3,4-tetrayl tetraacetate 
• 94898-39-2 (1S,2S,3S,4S,5R)-2-acetoxy-1-acetoxymethyl-3,4,5-tris(benzyloxy)cyclohexane 
• 112531-56-3 (3S,4S,5R)-3,4,5-tris(benzyloxy)-1-cyclohexene-1-methanol 

Relevant academic research and scientific papers

Construction of an Optically Active 7-Oxabicyclonon-4-en-3-one. Skeleton from D-Glucose, and Its Transformation to Some Pseudo-Hexopyranoses

A versatile chiral compound, (1R,6R,8R,9R)-8,9-isopropylidenedioxy-7-oxabicyclonon-4-en-3-one (6), was efficiently synthesized from D-glucose.The synthesis featured an intramolecular aldol cyclization of 3-C-acetylmethyl-3-deoxy-1,2-O-isopropyliden