201025-01-6

Upstream product

• 193271-77-1 (1S,2S,3S,5R,8R,10S,11S,12R)-10-methoxy-5-phenyl-4,6,9-trioxatetracyclo[10.2.1.0^2,11.0^3,8]pentadec-13-ene-2-carbaldehyde 
• 193271-74-8 methyl 4,6-O-benzylidene-2,3-dideoxy-3-C-formyl-α-D-erythro-hex-2-enopyranoside 
• 542-92-7 cyclopenta-1,3-diene 

Downstream Products

• 201025-02-7 (2R,4aR,6S,6aS,7S,9R,9aS,9bS)-6-Methoxy-2-phenyl-9a-propionyl-octahydro-cyclopenta[4,5]pyrano[3,2-d][1,3]dioxine-7,9-dicarbaldehyde 

Relevant academic research and scientific papers

Unsymmetrical ozonolysis of carbohydrate derived norbornene systems

The ozonolysis of carbohydrate derived norbornene systems in participating solvents demonstrated that different remote controlling factors could induce the regioselective fragmentation of the primary ozonide. The exo norbornene series afforded a complete

Enantiospecific approach toward pentalenolactone

The enantiospecific assembly of the pentalenolactones' carbon skeleton was achieved in 17 steps and 16% overall yield from methyl α-D- glucopyranoside. The synthetic strategy relies on two highly efficient key steps: an exo-diastereoselective Diels Alder

Enantiospecific approach to a quinane skeleton related to pentalenolactones

A novel and general approach has been delineated for the enantiomerically pure synthesis of the angularly fused tricyclic system of the pentalenolactone family of compounds. D-Glucose is used as starting material and a diasteroselective Diels-Alder reaction sets the elements for the ring junctions.