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45-O-(2-hydroxyethyl)-trallyl ziracin | 226074-44-8

中文名称
——
中文别名
——
英文名称
45-O-(2-hydroxyethyl)-trallyl ziracin
英文别名
——
45-O-(2-hydroxyethyl)-trallyl ziracin化学式
CAS
226074-44-8
化学式
C81H113Cl2NO39
mdl
——
分子量
1795.68
InChiKey
UXVCQXGPTQINCZ-ZPYULCSZSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

反应信息

  • 作为反应物:
    描述:
    45-O-(2-hydroxyethyl)-trallyl ziracin四(三苯基膦)钯三正丁基氢锡 、 zinc(II) chloride 作用下, 以 四氢呋喃 为溶剂, 生成
    参考文献:
    名称:
    Chemical modifications and structure activity studies of ziracin and related everninomicin antibiotics
    摘要:
    Chemical modifications of everninomicin antibiotics, particularly ziracin (1), were carried out to study the SARs as well as the chemical properties of this class of compounds. Use of allyl ether group for protection and selective deprotection of phenolic groups provided access to a variety of novel analogs of the title compounds, some of which exhibited the same high in vitro potency as the parent compounds. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(99)00163-8
  • 作为产物:
    描述:
    四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 生成 45-O-(2-hydroxyethyl)-trallyl ziracin
    参考文献:
    名称:
    Chemical modifications and structure activity studies of ziracin and related everninomicin antibiotics
    摘要:
    Chemical modifications of everninomicin antibiotics, particularly ziracin (1), were carried out to study the SARs as well as the chemical properties of this class of compounds. Use of allyl ether group for protection and selective deprotection of phenolic groups provided access to a variety of novel analogs of the title compounds, some of which exhibited the same high in vitro potency as the parent compounds. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(99)00163-8
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