102562-07-2

Upstream product

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

Downstream Products

• 102629-13-0 (1S,2S,3S,4S,5R)-2,3,4,5-tetrahydroxy-1-hydroxymethylcyclohexane 
• 112531-56-3 (3S,4S,5R)-3,4,5-tris(benzyloxy)-1-cyclohexene-1-methanol 
• 112473-47-9 (1R,2S,3S,4S,5R)-3,4,5-tris(benzyloxy)-2-hydroxycyclohexanecarbaldehyde 
• 112473-48-0 (3S,4S,5R)-3,4,5-Tris-benzyloxy-cyclohex-1-enecarbaldehyde 
• 94898-39-2 (1S,2S,3S,4S,5R)-2-acetoxy-1-acetoxymethyl-3,4,5-tris(benzyloxy)cyclohexane 
• 102629-12-9 (1R,2S,3S,4S,5S)-5-(acetoxymethyl)cyclohexane-1,2,3,4-tetrayl tetraacetate 

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

A NOVEL SYNTHESIS OF PSEUDO-α-L-ALTROPYRANOSE FROM D-GLUCOSE

(1R,6R,8R,9R)-8,9-Isopropylidenedioxy-3-oxo-7-oxabicyclo-non-4-ene, a highly functionalized bicyclic compound, has been synthesized from D-glucose employing an intramolecular aldol condensation as the key reaction, and a transformation of it into p