Microbial asymmetric reduction of α-hydroxyketones in the anti-Prelog selectivity
T Tsujigami, T Sugai, H Ohta
Index: Tsujigami, Toshikuni; Sugai, Takeshi; Ohta, Hiromichi Tetrahedron Asymmetry, 2001 , vol. 12, # 18 p. 2543 - 2549
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Citation Number: 40
Abstract
Yamadazyma farinosa IFO 10896 was found to reduce α-hydroxyketones bearing a phenyl ring to give optically active diols with anti-Prelog selectivity. The distance between the carbonyl group and the phenyl ring was shown to have an interesting effect on the reactivity and selectivity of the enzyme system.
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