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(R,R)-(+)-3-(2-oxopyrrodinyl-3-yl)pentanoic acid

中文名称
——
中文别名
——
英文名称
(R,R)-(+)-3-(2-oxopyrrodinyl-3-yl)pentanoic acid
英文别名
(3R)-3-[(3R)-2-oxopyrrolidin-3-yl]pentanoic acid
(R,R)-(+)-3-(2-oxopyrrodinyl-3-yl)pentanoic acid化学式
CAS
——
化学式
C9H15NO3
mdl
——
分子量
185.223
InChiKey
XKLHYSUJVDXHHP-RNFRBKRXSA-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):
    0.5
  • 重原子数:
    13
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.78
  • 拓扑面积:
    66.4
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    反-2-戊酸甲酯 在 lithium hydroxide 、 lithiumlithium diisopropyl amide 作用下, 以 四氢呋喃 为溶剂, 反应 3.0h, 生成 (R,R)-(+)-3-(2-oxopyrrodinyl-3-yl)pentanoic acid
    参考文献:
    名称:
    Diastereo- and Enantioselective Synthesis of g- and d-Lactams Bearing a Propionic Acid a-Side-Chain via Michael Addition of N-Dialkylamino Lactams to Enoates
    摘要:
    gamma- and- delta-Lactams [(R,R)-5a-e] bearing a propionic acid alpha-side-chain were synthesized in good overall yields (38 - 58 %, two steps) and diastereo- and enantiomeric excesses (de = greater than or equal to 96%, ee = 90 - greater than or equal to 96%) by 1,4-addition of metalated N-dialkylamino lactams [(S)-2a,b] to enoate Michael accepters (3) followed by saponification of the ester group and subsequent removal of the chiral auxiliary by reductive cleavage of the N-N-bond with lithium in liquid ammonia.
    DOI:
    10.3987/com-99-s83
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文献信息

  • Diastereo- and Enantioselective Synthesis of g- and d-Lactams Bearing a Propionic Acid a-Side-Chain via Michael Addition of N-Dialkylamino Lactams to Enoates
    作者:Dieter Enders、Pascal Teschner、Gerhard Raabe
    DOI:10.3987/com-99-s83
    日期:——
    gamma- and- delta-Lactams [(R,R)-5a-e] bearing a propionic acid alpha-side-chain were synthesized in good overall yields (38 - 58 %, two steps) and diastereo- and enantiomeric excesses (de = greater than or equal to 96%, ee = 90 - greater than or equal to 96%) by 1,4-addition of metalated N-dialkylamino lactams [(S)-2a,b] to enoate Michael accepters (3) followed by saponification of the ester group and subsequent removal of the chiral auxiliary by reductive cleavage of the N-N-bond with lithium in liquid ammonia.
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