Oxidation of sec-Alcohols to the Corresponding Ketones by Corynebacterium equfi
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概要
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Corynebacterium equi IFO 3730 was found to oxidize a wide variety of sec-oalcohols, including alkanols, substituted alkanols, alkenols and cyclic alcohols, in moderate to high yields. Among them, the sec-alcohols which have longer carbon chains were oxidized more smoothly than those with smaller numbers of carbon. Although both enantiomers of unsymmetrically disubstituted carbinols were oxidized, the S form of 2-dodecanol was converted to the corresponding ketone a little faster than the other enantiomer.
- 社団法人 日本農芸化学会の論文
著者
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Fujiwara Hidenori
Department Of Bioresources Science Graduate School Of Science And Technology Chiba University
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Ohta Hiromichi
Department Of Applied Chemistry School Of Engineering Nagoya University
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Tsuchihashi Gen-ichi
Department Of Chemistry Faculty Of Science And Technology Keio University
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