4.0 Article

Regio-and stereoselective benzylic hydroxylation to synthesize chiral tetrahydroquinolin-4-ol and tetrahydro-1H-benzo[b]azepin-5-ol with Pseudomonas plecoglossicidas

期刊

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.molcatb.2014.09.013

关键词

Asymmetric synthesis; Enzyme catalysis; Oxidation; Chiral sce-alcohols; Pseudomonas plecoglossicidas

资金

  1. Education Department of Guizhou Province [QSZHZ-2012-169, QJHRCTDZ-2012-03]
  2. Science and Technology Department of Guizhou Province [QKHGZ-2012-3078, QKHRZ-2013-47, QKHRCTD-2014-4002]
  3. National Nature Science Foundation of China (NSFC) [21162047, 21262051]
  4. New Century Excellent Talent of the Ministry of Education [NCET-13-1069]

向作者/读者索取更多资源

Two whole-cell biocatalysts were found to have C-H oxidation activity with high R-enantioselectivity on 1,2,3,4-tetrahydroquinoline (THQ) and 2,3,4,5-tetrahydro-1H-benzo[b]azepine (TBA). R-1,2,3,4-tetrahydroquinolin-4-ol ((R)-THQL) and R-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-ol ((R)-TBAL) were smoothly obtained with 82% yield in 99% e.e. and 99% yield in 98% e.e., respectively. (C) 2014 Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.0
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据