84622-39-9Relevant academic research and scientific papers
Enzyme-mediated enantioface-differentiating hydrolysis of α-substituted sulfur-containing cyclic ketone enol esters
Kume, Yasunari,Ohta, Hiromichi
, p. 6367 - 6370 (2007/10/02)
An enzymatic method for obtaining optically active α-substituted acyclic ketones is described. Pichia farinosa IAM 4682, a kind of yeast, hydrolyzed enol esters of sulfur-containing cyclic ketone with differentiation of the enantiotopic face. The resultin
Enzymes in organic synthesis. 30. Reaction conditions - control of enantiomeric purities. Horse liver alcohol dehydrogenase-catalyzed reductions of 2-alkylcyclohexanones and their thiopyran analogs
Jones, J. Bryan,Takemura, Tetsuo
, p. 77 - 80 (2007/10/02)
The effects of buffer, pH, reaction time, and / ratio on the enantiomeric purities of the alcohol products of horse liver alcohol dehydrogenase-catalyzed reductions of (+/-)-α-alkylcyclohexanones and -tetrahydrothiopyranones have been s
Enzymes in organic synthesis. 28. Reinvestigation of the horse liver alcohol dehydrogenase-catalyzed reductions of 2-alkylcyclohexanones. Identification of cis-alkylcyclohexanols as minor products.
Jones, J. Bryan,Takemura, Tetsuo
, p. 2950 - 2956 (2007/10/02)
The formation of cis-2-alkylcyclohexanol products from horse liver alcohol dehydrogenase-catalyzed reductions of 2-alkylcyclohexanones has been detected for the first time.The cis-alcohols are minor (/ and pH conditions possible, and by minimizing the reaction time.The results parallel the cis-alcohol formation observed previously with the analogous 3-alkyltetrahydropyran-4-one substrates.
