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Highly efficient chemoenzymatic syntheses of trans-2-aminocyclopentanol derivatives
Journal of Molecular Catalysis B: Enzymatic Pub Date : 2009 , DOI: 10.1016/j.molcatb.2009.01.006 Javier González-Sabín , Francisco Morís-Varas , Carmen Peña , Francisca Rebolledo , Vicente Gotor
Journal of Molecular Catalysis B: Enzymatic Pub Date : 2009 , DOI: 10.1016/j.molcatb.2009.01.006 Javier González-Sabín , Francisco Morís-Varas , Carmen Peña , Francisca Rebolledo , Vicente Gotor
A novel and efficient chemoenzymatic protocol for the preparation of both enantiomers of trans-2-aminocyclopentanol is described. The key steps of this strategy are the synthesis and subsequent Burkholderia cepacia lipase-catalyzed resolution of the racemic precursor trans-2-(diallylamino)cyclopentanol. In addition, a variety of diversely substituted derivatives are prepared from the enantiopure compounds isolated in the biotransformation by means of simple protection–deprotection reactions.
中文翻译:
反式-2-氨基环戊醇衍生物的高效化学合成
描述了用于制备反式-2-氨基环戊醇的两种对映异构体的新颖和有效的化学酶学方案。该策略的关键步骤是外消旋前体反式-2-(二烯丙基氨基)环戊醇的合成及随后的伯克霍尔德酒原脂肪酶催化的拆分。另外,通过简单的保护-脱保护反应,从生物转化中分离出的对映纯化合物制备了各种不同取代的衍生物。
更新日期:2017-01-31
中文翻译:
![](https://scdn.x-mol.com/jcss/images/paperTranslation.png)
反式-2-氨基环戊醇衍生物的高效化学合成
描述了用于制备反式-2-氨基环戊醇的两种对映异构体的新颖和有效的化学酶学方案。该策略的关键步骤是外消旋前体反式-2-(二烯丙基氨基)环戊醇的合成及随后的伯克霍尔德酒原脂肪酶催化的拆分。另外,通过简单的保护-脱保护反应,从生物转化中分离出的对映纯化合物制备了各种不同取代的衍生物。