摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

| 949165-94-0

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
949165-94-0
化学式
C44H64N6O12
mdl
——
分子量
869.025
InChiKey
NNWIPSNMUZWGKZ-JSGDOJDWSA-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:
    双(三甲基硅烷基)氨基钾 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以70%的产率得到
    参考文献:
    名称:
    Novel tethers in ketolide antibiotics
    摘要:
    Novel macrolide antibiotics which contain a methylerie unit between two nitrogen atoms of carbarnate groups or between two nitrogen atoms of one carbarnate and one urea group were synthesized using the Curtius rearrangement. Such linkers were shown to be stable under physiological conditions, and the resulting ketolides show potent in vitro and in vivo activity against macrolide-resistant respiratory pathogens. The SAR of various heterocycles and linkers was established. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.07.018
  • 作为产物:
    描述:
    喹喔啉-6-甲胺 、 生成
    参考文献:
    名称:
    Novel tethers in ketolide antibiotics
    摘要:
    Novel macrolide antibiotics which contain a methylerie unit between two nitrogen atoms of carbarnate groups or between two nitrogen atoms of one carbarnate and one urea group were synthesized using the Curtius rearrangement. Such linkers were shown to be stable under physiological conditions, and the resulting ketolides show potent in vitro and in vivo activity against macrolide-resistant respiratory pathogens. The SAR of various heterocycles and linkers was established. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.07.018
点击查看最新优质反应信息