首页> 外文期刊>Journal of the American Chemical Society >Enantioselective Synthesis of syn-and anti-1,3-Aminoalcohols via β-Aminoketones and Subsequent Reduction/Dynamic Kinetic Asymmetric Transformation
【24h】

Enantioselective Synthesis of syn-and anti-1,3-Aminoalcohols via β-Aminoketones and Subsequent Reduction/Dynamic Kinetic Asymmetric Transformation

机译:通过β-氨基酮和随后的还原/动力学动力学不对称转化反应,对映选择性合成正和反1,3-氨基醇

获取原文
获取原文并翻译 | 示例
           

摘要

β-Aminoketones obtained from imines in an organo-catalytic Mannich reaction were transformed to enantio- and diastereomerically pure 1,3-aminoalcohols with two stereogenic centers via a combined reduction/dynamic kinetic asymmetric transformation. Both syn and anti diastereomers were obtained in high yield, dr, and ee.
机译:在有机催化曼尼希反应中从亚胺获得的β-氨基酮通过还原/动态动力学不对称转化相结合,转化为具有两个立体中心的对映体和非对映体纯的1,3-氨基醇。 syn和抗非对映异构体均以高收率(dr和ee)获得。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2010年第43期|p.15182-15184|共3页
  • 作者单位

    Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, SE-106 91 Stockholm, Sweden;

    rnDepartment of Organic Chemistry, Arrhenius Laboratory, Stockholm University, SE-106 91 Stockholm, Sweden;

    rnDepartment of Organic Chemistry, Arrhenius Laboratory, Stockholm University, SE-106 91 Stockholm, Sweden;

    rnDepartment of Organic Chemistry, Arrhenius Laboratory, Stockholm University, SE-106 91 Stockholm, Sweden;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号