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Electrochemical Multi-Step Approach towards Isodityrosine, A Component of Biologically Important Cyclic Peptides

机译:电化学多步法制备异麦芽氨酸,一种重要的生物环状肽

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摘要

Isodityrosine, the diaryl ether moiety of the cyclic peptide class natural products responsible for fixation of their peptide conformations, has been successfully synthesized using electrochemical procedure for bromination, phenolic oxidation, and dehalogenation.
机译:异碘酪氨酸是环状肽类天然产物中负责固定其肽构象的二芳基醚部分,已使用溴化,酚氧化和脱卤的电化学方法成功合成。

著录项

  • 来源
  • 会议地点 Vienna(AT);Vienna(AT)
  • 作者

    K. Uno; T. Tanabe; S. Nishiyama;

  • 作者单位

    Department of Chemistry, Faculty of Science and Technology, Keio University Hiyoshi 3-14-1, Kohoku-ku, Yokohama 223-8522, Japan;

    Department of Chemistry, Faculty of Science and Technology, Keio University Hiyoshi 3-14-1, Kohoku-ku, Yokohama 223-8522, Japan;

    Department of Chemistry, Faculty of Science and Technology, Keio University Hiyoshi 3-14-1, Kohoku-ku, Yokohama 223-8522, Japan;

  • 会议组织
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物医学工程;
  • 关键词

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