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首页> 外文期刊>Journal of molecular catalysis, B. Enzymatic >Diastereoselective reduction of 1-(4-fluorophenyl)-3(R)-[3-oxo-3-(4-fluorophenyl)-propyl]-4(S)-(4-hydroxyphenyl)azetidin-2-one to Ezetimibe by the whole cell catalyst Rhodococcus fascians MO22
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Diastereoselective reduction of 1-(4-fluorophenyl)-3(R)-[3-oxo-3-(4-fluorophenyl)-propyl]-4(S)-(4-hydroxyphenyl)azetidin-2-one to Ezetimibe by the whole cell catalyst Rhodococcus fascians MO22

机译:将1-(4-氟苯基)-3(R)-[3-氧代-3-(4-氟苯基)-丙基] -4(S)-(4-羟基苯基)氮杂环丁烷-2-酮非对映选择性还原为依泽替米贝全细胞催化剂Rhodococcus fascians MO22

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摘要

The asymmetric microbial reduction of 1-(4-fluorophenyl)-3(R)-[3-oxo-3-(4-fluorophenyl)-propyl]-4(S)-(4-hydroxyphenyl)azetidin-2-one to 1-(4-fIuorophenyl)-3(R)-[3(S)-hydroxy-3-(4-fIuorophenyl)-propyl]-4(S)- (4-hydroxyphenyl)azetidin-2-one (Ezetimibe) by Rhodococcus fascians MO22 is described. The catalytic capability of the microorganism for reduction has been examined also with protected ketone, an intermediate from chemical synthesis of Ezetimibe. Various parameters of the bioreduction have been optimized: the strain converted 94.8% of ketone and 63% of protected ketone into Ezetimibe with the same de of 99.9%. In the later case, two chemical steps are replaced with a single biotransformation.
机译:1-(4-氟苯基)-3(R)-[3-氧代-3-(4-氟苯基)-丙基] -4(S)-(4-羟基苯基)氮杂环丁烷-2-酮的不对称微生物还原1-(4-氟苯基)-3(R)-[3(S)-羟基-3-(4-氟苯基)-丙基] -4(S)-(4-羟基苯基)氮杂环丁烷-2-酮(依泽替米贝)由Rhodococcus fascians对MO22进行了描述。还已经用受保护的酮(来自依泽替米贝的化学合成的中间体)检查了微生物还原的催化能力。生物还原的各种参数已得到优化:该菌株将94.8%的酮和63%的受保护的酮转化为依泽替米贝,转化率相同,为99.9%。在后一种情况下,将两个化学步骤替换为一次生物转化。

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