140460-25-9

Upstream product

• 823-18-7 cis-1,3-cyclohexanediol 
• 100-44-7 benzyl chloride 
• 504-01-8 cyclohexane-1,3-diol 
• 100-39-0 benzyl bromide 
• 130256-46-1 (3S,5S)-5-benzyloxy-1-cyclohexen-3-ol 
• 130256-36-9 (1S,3S,5R)-1-acetoxy-5-benzyloxy-3-cyclohexanol 
• 131245-94-8 (S)-5-benzyloxy-2-cyclohexen-1-one 
• 130256-34-7 meso-1,3-cis,3,5-cis-1,3-diacetoxy-5-benzyloxycyclohexane 

Relevant academic research and scientific papers

Intramolecular benzyl-benzyl interactions in protonated benzyl diethers in the gas phase. Effects of internal hydrogen bonding

Protonated molecules of a variety of benzyl diethers, produced by chemical ionization (CI), undergo a unique rearrangement yielding relatively abundant mlz 181 C14H13+ ions, both in the ion source and under collision-induc

Enantioselective synthesis of (1S,3S,5R)-1-acetoxy-5-benzyl-oxycyclohexan-3-ol and its application to the synthesis of compactin lactone moiety and quinic acid

Porcine liver esterase (PLE)-catalyzed asymmetric hydrolysis of meso-1,3-cis,3,5-cis-1,3-diacetoxy-5-benzyloxycyclohexane 1 afforded (1S,3S,5R)-2 of 87% e.e. Starting from this compound, compactin lactone moiety 17A and its C-6 diastereomer 17B were diast