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14-Phenacyl-4,12-dioxa-14,17-diazahexacyclo[11.11.1.02,11.05,10.015,24.016,21]pentacosa-2(11),5,7,9,15(24),16(21),17,19,22-nonaen-3-one | 1296206-50-2

中文名称
——
中文别名
——
英文名称
14-Phenacyl-4,12-dioxa-14,17-diazahexacyclo[11.11.1.02,11.05,10.015,24.016,21]pentacosa-2(11),5,7,9,15(24),16(21),17,19,22-nonaen-3-one
英文别名
14-phenacyl-4,12-dioxa-14,17-diazahexacyclo[11.11.1.02,11.05,10.015,24.016,21]pentacosa-2(11),5,7,9,15(24),16(21),17,19,22-nonaen-3-one
14-Phenacyl-4,12-dioxa-14,17-diazahexacyclo[11.11.1.02,11.05,10.015,24.016,21]pentacosa-2(11),5,7,9,15(24),16(21),17,19,22-nonaen-3-one化学式
CAS
1296206-50-2
化学式
C29H20N2O4
mdl
——
分子量
460.489
InChiKey
DLRXFCNWHPLNPR-UHFFFAOYSA-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):
    5.2
  • 重原子数:
    35
  • 可旋转键数:
    3
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    68.7
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为产物:
    参考文献:
    名称:
    The unprecedented C-alkylation and tandem C-/O-alkylation of phenanthrolinium salts with cyclic 1,3-dicarbonyl compounds
    摘要:
    N-p-Nitrobenzyl- or N-phenacylphenanthrolinium bromides reacted with a series of cyclic 1,3-dicarbonyl compounds in acetonitrile in the presence of triethylamine as base catalyst to give the unprecedented C-alkylated products and tandem alkylated/intramolecular O-alkylated oxazabicyclic compounds according to the structure of cyclic 1,3-dicarbonyl compounds. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2011.02.063
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文献信息

  • The unprecedented C-alkylation and tandem C-/O-alkylation of phenanthrolinium salts with cyclic 1,3-dicarbonyl compounds
    作者:Hui Li、Chao-Guo Yan
    DOI:10.1016/j.tet.2011.02.063
    日期:2011.4
    N-p-Nitrobenzyl- or N-phenacylphenanthrolinium bromides reacted with a series of cyclic 1,3-dicarbonyl compounds in acetonitrile in the presence of triethylamine as base catalyst to give the unprecedented C-alkylated products and tandem alkylated/intramolecular O-alkylated oxazabicyclic compounds according to the structure of cyclic 1,3-dicarbonyl compounds. (C) 2011 Elsevier Ltd. All rights reserved.
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