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10,23:11,22-diepoxy-4b,8b,12b,16b,20b,24b,24d,24e-octamethyl-4b,8b,10,10a,11,12b,16b,20b,22,22a,23,24b,24d,24e-tetradecahydrobisbenzo[5,6]indeno[1',2',3':3,4]pentaleno[1,2-b:1',2'-k]tetracene | 1354700-37-0

中文名称
——
中文别名
——
英文名称
10,23:11,22-diepoxy-4b,8b,12b,16b,20b,24b,24d,24e-octamethyl-4b,8b,10,10a,11,12b,16b,20b,22,22a,23,24b,24d,24e-tetradecahydrobisbenzo[5,6]indeno[1',2',3':3,4]pentaleno[1,2-b:1',2'-k]tetracene
英文别名
syn-bis-TBTQ diepoxide
10,23:11,22-diepoxy-4b,8b,12b,16b,20b,24b,24d,24e-octamethyl-4b,8b,10,10a,11,12b,16b,20b,22,22a,23,24b,24d,24e-tetradecahydrobisbenzo[5,6]indeno[1',2',3':3,4]pentaleno[1,2-b:1',2'-k]tetracene化学式
CAS
1354700-37-0
化学式
C58H50O2
mdl
——
分子量
779.034
InChiKey
SZZMPYKQFKGYQP-CJBMNHIUSA-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:
    10,23:11,22-diepoxy-4b,8b,12b,16b,20b,24b,24d,24e-octamethyl-4b,8b,10,10a,11,12b,16b,20b,22,22a,23,24b,24d,24e-tetradecahydrobisbenzo[5,6]indeno[1',2',3':3,4]pentaleno[1,2-b:1',2'-k]tetracene对甲苯磺酸 作用下, 以 甲苯 为溶剂, 反应 0.33h, 以38%的产率得到2,3-diformyl-4b,8b,12b,12d-tetramethyl-4b,8b,12b,12d-tetrahydrodibenzo[2,3:4,5]pentaleno[1,6-ab]indene
    参考文献:
    名称:
    Single-wing Extended Tribenzotriquinacenes via Bowl-shaped Dehydrobenzene and Isobenzofuran Tribenzotriquinacene Derivatives
    摘要:
    Monoaryne and monoisobenzofuran analogues of a C-3v-symmetrical tribenzotriquinacene (TBTQ) were generated in situ and trapped with various dienes and dienophiles, respectively. In this way, a series of single-wing extended TBTQ derivatives bearing the bowl-shaped TBTQ unit in different topographical expositions have become accessible. This includes some novel tribenzotriquinacene "dimers", in which two TBTQ bowls are attached in syn- or anti-orientation at the terminal positions of rigid linker units. Several of these compounds have been characterized by both spectroscopy and X-ray structural analysis. The efficient access to the TBTQ "dimers" studies of novel container compounds and supramolecular architectures.
    DOI:
    10.1021/jo2022668
  • 作为产物:
    描述:
    10,13-epoxy-4b,8b,14b,14d-tetramethyl-4b,8b,10,13,14b,14d-hexahydrobenzo[5,6]indeno[1',2',3':3,4]pentaleno[1,2-b]naphthalene 在 3,6-二-2-吡啶基-1,2,4,5-四嗪 作用下, 以 甲苯 为溶剂, 反应 2.0h, 以61%的产率得到10,23:11,22-diepoxy-4b,8b,12b,16b,20b,24b,24d,24e-octamethyl-4b,8b,10,10a,11,12b,16b,20b,22,22a,23,24b,24d,24e-tetradecahydrobisbenzo[5,6]indeno[1',2',3':3,4]pentaleno[1,2-b:1',2'-k]tetracene
    参考文献:
    名称:
    Single-wing Extended Tribenzotriquinacenes via Bowl-shaped Dehydrobenzene and Isobenzofuran Tribenzotriquinacene Derivatives
    摘要:
    Monoaryne and monoisobenzofuran analogues of a C-3v-symmetrical tribenzotriquinacene (TBTQ) were generated in situ and trapped with various dienes and dienophiles, respectively. In this way, a series of single-wing extended TBTQ derivatives bearing the bowl-shaped TBTQ unit in different topographical expositions have become accessible. This includes some novel tribenzotriquinacene "dimers", in which two TBTQ bowls are attached in syn- or anti-orientation at the terminal positions of rigid linker units. Several of these compounds have been characterized by both spectroscopy and X-ray structural analysis. The efficient access to the TBTQ "dimers" studies of novel container compounds and supramolecular architectures.
    DOI:
    10.1021/jo2022668
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