102108-37-2

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 5891-21-4 5-chloro-2-pentanone 
• 24156-97-6 (2S)-(+)-5-chloro-2-(tetrahydropyranyl-2-oxy)pentane 
• 99212-19-8 (S)-(+)-5-chloropentan-2-ol 
• 108-24-7 acetic anhydride 
• 102108-36-1 (7S)-(+)-3-hydroxy-1-phenyl-7-(tetrahydropyranyl-2-oxy)oct-1-ene 

Downstream Products

• 102108-38-3 (7S)-(+)-3-acetoxy-7-hydroxy-1-phenyloct-1-ene 
• 102208-96-8 phenyl (2S,6S)-(cis-6-methyltetrahydropyran-2-yl)acetate 
• 102208-93-5 (2R,6S)-(E)-2-(trans-6-methyltetrahydropyran-2-yl)-1-phenylethene 
• 102108-39-4 (2S,6S)-(E)-2-(cis-6-methyltetrahydropyran-2-yl)-1-phenylethene 
• 102208-95-7 (2S,6S)-(cis-6-methyltetrahydropyran-2-yl)acetophenone 
• 102208-94-6 (2R,6S)-(trans-6-methyltetrahydropyran-2-yl)acetophenone 
• 102108-40-7 phenyl (2R,6S)-(trans-6-methyltetrahydropyran-2-yl)acetate 

Relevant academic research and scientific papers

Organic Synthesis with Enzymes. 3. TBADH-Catalyzed Reduction of Chloro Ketones. Total Synthesis of (+)-(S,S)-(cis-6-Methyltetrahydropyran-2-yl)acetic Acid: A Civet Constituent

Highly enantioselective reduction of aliphatic chloro ketones catalyzed by Thermoanaerobium brockii alcohol dehydrogenase (TBADH) afforded the corresponding S chloro alcohols, which are new and useful chiral bifunctional building blocks.The synthetic pote