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Asymmetric synthesis of amino-benzothiazol derivatives by additions of 2-lithiated benzothiazoles to (S)-N-t-butylsulfinyl-ketimines

机译:通过添加2锂苯并噻唑酯至(S)-N-T-丁基磺酰基 - 酮亚胺,不对称合成氨基 - 苯并噻唑衍生物

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摘要

The reactions between lithium-benzothiazoles and (S)-N-tert-butanesulfinylketimines have been found to be of general synthetic importance for asymmetric preparation of previously unknown type of amino-benzothiazol derivatives of high pharmaceutical potential. In most cases, the reactions proceed with excellent diastereoselectivities and good isolated yields of the target compounds rendering the developed procedure of high synthetic value and immediate practical use.
机译:已经发现锂 - 苯并噻唑和(S)-N-叔丁磺基磺酰基亚胺的反应具有一般的合成重要性,用于高药物潜力的先前未知的氨基 - 苯并噻唑衍生物的不对称制剂。 在大多数情况下,反应采用优异的非对映心选择性和良好的分离产量,其靶化合物提供高合成值和立即实际使用的开发程序。

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  • 来源
    《RSC Advances》 |2015年第5期|共7页
  • 作者单位

    Nanjing Univ Sch Chem &

    Chem Engn State Key Lab Coordinat Chem Nanjing 210093 Jiangsu Peoples R China;

    Nanjing Univ Sch Chem &

    Chem Engn State Key Lab Coordinat Chem Nanjing 210093 Jiangsu Peoples R China;

    Nanjing Univ Sch Chem &

    Chem Engn State Key Lab Coordinat Chem Nanjing 210093 Jiangsu Peoples R China;

    Nanjing Univ Sch Chem &

    Chem Engn State Key Lab Coordinat Chem Nanjing 210093 Jiangsu Peoples R China;

    Univ Basque Country UPV EHU Fac Chem Dept Organ Chem 1 San Sebastian 20018 Spain;

    Nanjing Univ Sch Chem &

    Chem Engn State Key Lab Coordinat Chem Nanjing 210093 Jiangsu Peoples R China;

    Nanjing Univ Sch Chem &

    Chem Engn State Key Lab Coordinat Chem Nanjing 210093 Jiangsu Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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