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(2S,4R)-2-[(E)-2-(3-Hydroxymethyl-isoxazol-5-yl)-vinyl]-4-methanesulfonyloxy-pyrrolidine-1-carboxylic acid allyl ester | 326605-39-4

中文名称
——
中文别名
——
英文名称
(2S,4R)-2-[(E)-2-(3-Hydroxymethyl-isoxazol-5-yl)-vinyl]-4-methanesulfonyloxy-pyrrolidine-1-carboxylic acid allyl ester
英文别名
——
(2S,4R)-2-[(E)-2-(3-Hydroxymethyl-isoxazol-5-yl)-vinyl]-4-methanesulfonyloxy-pyrrolidine-1-carboxylic acid allyl ester化学式
CAS
326605-39-4
化学式
C15H20N2O7S
mdl
——
分子量
372.399
InChiKey
LBPNRJBLGAFZEH-TZMCWYRMSA-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

计算性质

  • 辛醇/水分配系数(LogP):
    0.92
  • 重原子数:
    25.0
  • 可旋转键数:
    7.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    119.17
  • 氢给体数:
    1.0
  • 氢受体数:
    8.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Synthesis and biological activity of 1β-methyl-2-[5′-isoxazoloethenylpyrrolidin-3′-ylthio]carbapenems
    摘要:
    A new series of 1 beta -methylcarbapenems 1a-i bearing isoxazoloethenyl groups on the pyrrolidine ring has been prepared and evaluated for in vitro antibacterial activity and stability to DHP-I. Most compounds showed excellent antibacterial activity and high stability to DHP-I superior to that of meropenem. Of these new carbapenems, 1a,b,h exhibited the best combination of antibacterial activity and DHP-I stability. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(00)00575-8
  • 作为产物:
    描述:
    5-[(E)-2-((2S,4R)-1-Allyloxycarbonyl-4-methanesulfonyloxy-pyrrolidin-2-yl)-vinyl]-isoxazole-3-carboxylic acid methyl ester 在 sodium tetrahydroborate 、 乙醇 作用下, 以 四氢呋喃 为溶剂, 反应 7.0h, 以89%的产率得到(2S,4R)-2-[(E)-2-(3-Hydroxymethyl-isoxazol-5-yl)-vinyl]-4-methanesulfonyloxy-pyrrolidine-1-carboxylic acid allyl ester
    参考文献:
    名称:
    Synthesis and biological activity of 1β-methyl-2-[5′-isoxazoloethenylpyrrolidin-3′-ylthio]carbapenems
    摘要:
    A new series of 1 beta -methylcarbapenems 1a-i bearing isoxazoloethenyl groups on the pyrrolidine ring has been prepared and evaluated for in vitro antibacterial activity and stability to DHP-I. Most compounds showed excellent antibacterial activity and high stability to DHP-I superior to that of meropenem. Of these new carbapenems, 1a,b,h exhibited the best combination of antibacterial activity and DHP-I stability. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(00)00575-8
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