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Synthesis of fluorescent 7-amino-2,1-benzothiazines and total synthesis of buddledone A.

机译:荧光7-氨基-2,1-苯并噻嗪的合成和buddledone A的全合成。

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摘要

The development of new fluorescent compounds has been reported continuously due to their application as sensors and optical devices for material, biological and chemical applications. This dissertation reports the syntheses of several novel fluorescent 7-amino-2,1-benzothiazines using palladium-catalyzed N-arylation of a sulfoximine with various 4-amino-2-halobenzaldehydes and the reaction between 7-fluoro-2,1-benzothiazine with amines. Structural modification of these compounds at C-7 provided a slight improvement in fluorescent properties.;In the second chapter, the total synthesis of buddledone A using ring-closing metathesis as a key step is presented. Efforts toward synthesis of zerumbone from buddledone A using several conditions were reported. Unfortunately, the conversion of buddledone A to zerumbone failed to give the desired product.
机译:由于新型荧光化合物作为材料,生物和化学应用的传感器和光学设备的应用,一直在不断报道其发展。这篇论文报道了使用钯催化的亚砜亚胺与各种4-氨基-2-卤代苯甲醛的N-芳基化反应,合成了几种新型的荧光7-氨基-2,1-苯并噻嗪,以及7-氟-2,1-苯并噻嗪之间的反应。与胺。这些化合物在C-7处的结构修饰使荧光性质略有改善。;在第二章中,介绍了以闭环复分解为关键步骤的芽孢酮A的全合成。报道了使用几种条件从芽孢酮A合成泽隆骨的努力。不幸的是,将芽孢酮A转化为蛇骨素未能得到所需的产物。

著录项

  • 作者

    Yongpruksa, Nattawut.;

  • 作者单位

    University of Missouri - Columbia.;

  • 授予单位 University of Missouri - Columbia.;
  • 学科 Chemistry Biochemistry.;Health Sciences Medical Ethics.;Chemistry Organic.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 192 p.
  • 总页数 192
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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