首页> 外文期刊>Journal of molecular catalysis, B. Enzymatic >Enzymatic resolution of a chiral chlorohydrin precursor for (R)-α-lipoic acid synthesis via lipase catalyzed enantioselective transacylation with vinyl acetate
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Enzymatic resolution of a chiral chlorohydrin precursor for (R)-α-lipoic acid synthesis via lipase catalyzed enantioselective transacylation with vinyl acetate

机译:手性氯醇前体通过脂肪酶催化乙酸乙烯酯对映选择性转酰基反应合成(R)-α-硫辛酸的手性拆分

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摘要

Anew and efficient process was developed by lipase-catalyzed transacylation to resolve ethyl 8-chloro-6-hydroxy octanoate (ECHO) to produce an important chiral precursor for the synthesis of (R)-α-lipoic acid. After optimization of biocatalyst, solvent, acyl donor, temperature and enzyme loading, (S)-O-acetylated ECHO was achieved in 94% ee, 35% isolated yield and 38 g L~(-1) d~(-1) space-time yield using Novozym 435 as biocatalyst. Subsequently, the enzymatic resolution reaction was successfully repeated for 7 batches, retaining over 40% conversions.
机译:通过脂肪酶催化的酰基转移反应开发了一种新的高效方法,以分解8-氯-6-羟基辛酸乙酯(ECHO),以生产重要的手性前体,用于合成(R)-α-硫辛酸。通过优化生物催化剂,溶剂,酰基供体,温度和酶的负载量,在94%ee,35%分离产率和38 g L〜(-1)d〜(-1)空间中获得(S)-O-乙酰化的ECHO。 Novozym 435作为生物催化剂的实时收率。随后,成功地重复进行了7批酶解反应,保留了40%以上的转化率。

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