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(+)-(2S,3S,3aR)-3a-cyclohexyloxy-1,2,3,3a-tetrahydrocyclopent[a]indene-2,3-diyl diacetate | 1173722-73-0

中文名称
——
中文别名
——
英文名称
(+)-(2S,3S,3aR)-3a-cyclohexyloxy-1,2,3,3a-tetrahydrocyclopent[a]indene-2,3-diyl diacetate
英文别名
[(1S,2S,8bR)-1-acetyloxy-8b-cyclohexyloxy-2,3-dihydro-1H-cyclopenta[a]inden-2-yl] acetate
(+)-(2S,3S,3aR)-3a-cyclohexyloxy-1,2,3,3a-tetrahydrocyclopent[a]indene-2,3-diyl diacetate化学式
CAS
1173722-73-0
化学式
C22H26O5
mdl
——
分子量
370.445
InChiKey
GGQPRMGIWGPFAU-FDFHNCONSA-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):
    3.3
  • 重原子数:
    27
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    61.8
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Synthesis of a Core Carbon Framework of Cyanosporasides A and B
    摘要:
    Treatment of 3-(2-ethynylphenyl)prop-2-ynyl benzenesulfinate with 2.5-mol % of [RhCl(CO)(2)](2) at 40 degrees C under an atmosphere of CO effected the successive 2,3-sigmatropic rearrangement and carbonylative [2 + 2 + 1] ring-closing reaction to afford the 8-(phenylsulfonyl)-1H-cyclopent[a]-inden-2-one in a high yield. Chemical modification of the ring-closed product via lipase-mediated optical resolution produced tile optically active 3-acetoxy-3a-cyclohexyloxy-3,3a-dihydrocyclopent[a]indene skeleton, the core carbon framework of cyanosporasides A and B.
    DOI:
    10.1021/jo901141t
  • 作为产物:
    描述:
    (2RS,3RS,3aRS)-3a-cyclohexyloxy-8-(phenylsulfonyl)-1,2,3,3a-tetrahydrocyclopent[a]indene-2,3-diyl diacetate 在 偶氮二异丁腈三正丁基氢锡盐酸 作用下, 以 为溶剂, 反应 24.0h, 生成 (+)-(2S,3S,3aR)-3a-cyclohexyloxy-1,2,3,3a-tetrahydrocyclopent[a]indene-2,3-diyl diacetate
    参考文献:
    名称:
    Synthesis of a Core Carbon Framework of Cyanosporasides A and B
    摘要:
    Treatment of 3-(2-ethynylphenyl)prop-2-ynyl benzenesulfinate with 2.5-mol % of [RhCl(CO)(2)](2) at 40 degrees C under an atmosphere of CO effected the successive 2,3-sigmatropic rearrangement and carbonylative [2 + 2 + 1] ring-closing reaction to afford the 8-(phenylsulfonyl)-1H-cyclopent[a]-inden-2-one in a high yield. Chemical modification of the ring-closed product via lipase-mediated optical resolution produced tile optically active 3-acetoxy-3a-cyclohexyloxy-3,3a-dihydrocyclopent[a]indene skeleton, the core carbon framework of cyanosporasides A and B.
    DOI:
    10.1021/jo901141t
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