482635-97-2

Upstream product

• 482635-96-1 (3R,4S,5R,6S)-3,6-dibenzyloxy-7-hydroxy-4,5-(isopropylidenedioxy)heptanoic acid 
• 74-88-4 methyl iodide 
• 482635-93-8 r-1-[(tert-butyldimethylsilyl)oxy]-trans-3,trans-6-dibenzyloxy-cis-4,cis-5-(isopropylidenedioxy)cycloheptane 
• 482635-92-7 cis-5-[(tert-butyldimethylsilyl)oxy]-trans-3,trans-7-dibenzyloxy-r-1,cis-2-cyclo-heptanediol 
• 1053694-71-5 ((3aS,4R,8S,8aR)-4,8-Bis-benzyloxy-2,2-dimethyl-4,5,8,8a-tetrahydro-3aH-cyclohepta[1,3]dioxol-6-yloxy)-trimethyl-silane 
• 482635-91-6 trans-5-[(tert-butyldimethylsilyl)oxy]-r-3,cis-7-dibenzyloxycycloheptene 
• 482635-94-9 trans-3,trans-6-dibenzyloxy-cis-4,cis-5-(isopropylidenedioxy)cycloheptan-r-1-ol 
• 482635-95-0 r-3,cis-6-dibenzyloxy-trans-4,trans-5-(isopropylidenedioxy)cycloheptan-1-one 
• 134780-03-3 meso-(1R,4R,6R)-6-<(tert-Butyldimethylsilyl)oxy>-2-cycloheptene-1,4-diol 
• 100-39-0 benzyl bromide 

Downstream Products

• 482635-98-3 methyl (3S,4R,5S)-[5-benzyloxy-3,4-(isopropylidenedioxy)tetrahydropyran-2-yl]acetate 

Relevant academic research and scientific papers

Enantioselective Deprotonation of meso-Cycloheptanone Derivative: Application to the Synthesis of a Potential Intermediate for Pseudomonic Acid B

(Matrix Presented) A novel synthetic path to a potential intermediate for the synthesis of pseudomonic acid B was established by employing enantioselective deprotonation of a meso-cycloheptanone derivative bearing hydroxy groups at the 3,4,5,6-positions w