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New stereoselective synthesis of thiamphenicol and florfenicol from enantiomerically pure cyanohydrin: a chemo-enzymatic approach

机译:从对映体纯的氰醇中新立体选择性合成噻吩酚和氟苯尼考:一种化学酶方法

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摘要

Thiamphenicol and florfenicol have been synthesized stereoselectively from enantiomerically pure 4-methylsulfanyl-mandelonitrile, which was obtained by hydrocyanation reaction of 4-methylsulfanyl-benzaldehyde catalyzed by (R)-hydroxynitrile Iyase of Badamu (Prunus communis L. var. dulcis Borkh, almond from Xinjiang, China). It was found to be a highly effective bio-catalyst for this reaction after an extensive screening. (C) 2008 Elsevier Ltd. All rights reserved.
机译:甲砜霉素和氟苯尼考是通过对映体纯的4-甲基硫烷基-扁桃腈立体选择性合成的,该化合物是通过Badamu的(R)-羟基腈腈酶催化的4-甲基硫烷基-苯甲醛的氢氰化反应制得的。中国新疆)。经过广泛筛选后,发现它是该反应的高效生物催化剂。 (C)2008 Elsevier Ltd.保留所有权利。

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