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(3R,3aR,9aS,9bR)-3,6-Dimethyl-9-methylene-3-phenylselanyl-3a,4,5,7,8,9,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one | 90807-58-2

中文名称
——
中文别名
——
英文名称
(3R,3aR,9aS,9bR)-3,6-Dimethyl-9-methylene-3-phenylselanyl-3a,4,5,7,8,9,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one
英文别名
(3R,3aR,9aS,9bR)-3,6-dimethyl-9-methylidene-3-phenylselanyl-4,5,7,8,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-2-one
(3R,3aR,9aS,9bR)-3,6-Dimethyl-9-methylene-3-phenylselanyl-3a,4,5,7,8,9,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one化学式
CAS
90807-58-2
化学式
C21H24O2Se
mdl
——
分子量
387.38
InChiKey
AWNIHDQAMFWRME-XODKDNOYSA-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):
    3.81
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (3R,3aR,9aS,9bR)-3,6-Dimethyl-9-methylene-3-phenylselanyl-3a,4,5,7,8,9,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one双氧水 作用下, 以 四氢呋喃溶剂黄146 为溶剂, 以100%的产率得到(3aS,9aS,9bS)-6-Methyl-3,9-dimethylene-3a,4,5,7,8,9,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one
    参考文献:
    名称:
    TOTAL SYNTHESES OF MOKKO LACTONE, DEHYDROCOSTUS LACTONE, AND EREMANTHIN
    摘要:
    以1-oxoeudesm-2-eno-13,6α-内酯为原料,经过7步合成了一系列在A环上具有共同结构单元的愈创木酚内酯,如木香内酯、脱氢木香内酯和eremanthin。关键步骤涉及 1β-mesyloxyeudesm-4(14)-eno-13,6α-内酯的溶剂分解重排。
    DOI:
    10.1246/cl.1984.493
  • 作为产物:
    描述:
    (11S)-1-oxoeudesm-2-eno-12,6α-lactone 在 吡啶 、 lithium tri-t-butoxyaluminum hydride 、 作用下, 以 四氢呋喃溶剂黄146 为溶剂, 反应 8.5h, 生成 (3R,3aR,9aS,9bR)-3,6-Dimethyl-9-methylene-3-phenylselanyl-3a,4,5,7,8,9,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one
    参考文献:
    名称:
    Guaianolides as Immunomodulators. Synthesis and Biological Activities of Dehydrocostus Lactone, Mokko Lactone, Eremanthin, and Their Derivatives
    摘要:
    The naturally occurring guaianolides, namely mokko lactone (1), dehydrocostus lactone (2), eremanthin (3), and related guaianolides, 16, 17, 21, 22, 28-31, 33, 36, 37, and 39, have been synthesized starting from I-a-santonin in an effort to examine their structure-activity relationship as inhibitors of the killing function of cytotoxic T lymphocytes (CTL) and the induction of intercellular adhesion molecule-1 (ICAM-1). It was observed during the present study that the guaianolides possessing an alpha-methylene gamma-lactone moiety, i.e., 2, 3, 30, 33, 37, and 39, exhibited significant inhibitory activity toward the killing function of CTL and the induction of ICAM-1.
    DOI:
    10.1021/np980092u
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文献信息

  • TOTAL SYNTHESES OF MOKKO LACTONE, DEHYDROCOSTUS LACTONE, AND EREMANTHIN
    作者:Masayoshi Ando、Akio ONO、Kahei Takase
    DOI:10.1246/cl.1984.493
    日期:1984.4.5
    A series of guaianolides such as mokko lactone, dehydrocostus lactone, and eremanthin which posses a common structural unit in A ring have been synthesized from 1-oxoeudesm-2-eno-13,6α-lactone in 7 steps. The key step involves solvolytic rearrangement of 1β-mesyloxyeudesm-4(14)-eno-13,6α-lactone.
    以1-oxoeudesm-2-eno-13,6α-内酯为原料,经过7步合成了一系列在A环上具有共同结构单元的愈创木酚内酯,如木香内酯、脱氢木香内酯和eremanthin。关键步骤涉及 1β-mesyloxyeudesm-4(14)-eno-13,6α-内酯的溶剂分解重排。
  • Guaianolides as Immunomodulators. Synthesis and Biological Activities of Dehydrocostus Lactone, Mokko Lactone, Eremanthin, and Their Derivatives
    作者:Saori Yuuya、Hisahiro Hagiwara、Toshio Suzuki、Masayoshi Ando、Atsushi Yamada、Kouji Suda、Takao Kataoka、Kazuo Nagai
    DOI:10.1021/np980092u
    日期:1999.1.1
    The naturally occurring guaianolides, namely mokko lactone (1), dehydrocostus lactone (2), eremanthin (3), and related guaianolides, 16, 17, 21, 22, 28-31, 33, 36, 37, and 39, have been synthesized starting from I-a-santonin in an effort to examine their structure-activity relationship as inhibitors of the killing function of cytotoxic T lymphocytes (CTL) and the induction of intercellular adhesion molecule-1 (ICAM-1). It was observed during the present study that the guaianolides possessing an alpha-methylene gamma-lactone moiety, i.e., 2, 3, 30, 33, 37, and 39, exhibited significant inhibitory activity toward the killing function of CTL and the induction of ICAM-1.
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