摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

N-formyl-2,3-dimethoxy-5,6,7,8-tetrahydrodiben[c,e]azocine | 65762-80-3

中文名称
——
中文别名
——
英文名称
N-formyl-2,3-dimethoxy-5,6,7,8-tetrahydrodiben[c,e]azocine
英文别名
6-formyl-2,3-dimethoxy-5,6,7,8-tetrahydro-dibenzo[c,e]azocine;4,5-Dimethoxy-9-azatricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaene-9-carbaldehyde
N-formyl-2,3-dimethoxy-5,6,7,8-tetrahydrodiben[c,e]azocine化学式
CAS
65762-80-3
化学式
C18H19NO3
mdl
——
分子量
297.354
InChiKey
HXODZEJUZYAFAI-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):
    2.8
  • 重原子数:
    22
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    38.8
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 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:
    N-formyl-2,3-dimethoxy-5,6,7,8-tetrahydrodiben[c,e]azocine 在 lithium aluminium tetrahydride 作用下, 以 四氢呋喃 为溶剂, 反应 15.0h, 以94%的产率得到buflavine
    参考文献:
    名称:
    Synthesis of Amaryllidaceae alkaloids, siculine, oxocrinine, epicrinine, and buflavine
    摘要:
    Three crinane type of alkaloids isolated from Amaryllidaceae family were synthesized by taking advantage of the PIFA-mediated intramolecular p-p' diphenol coupling reaction of norbelladine derivatives. Furthermore, buflavine was also prepared by using the p-p' diphenol coupling followed by dienone-phenol rearrangement as a key step. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2004.03.087
  • 作为产物:
    参考文献:
    名称:
    Synthesis of Amaryllidaceae alkaloids, siculine, oxocrinine, epicrinine, and buflavine
    摘要:
    Three crinane type of alkaloids isolated from Amaryllidaceae family were synthesized by taking advantage of the PIFA-mediated intramolecular p-p' diphenol coupling reaction of norbelladine derivatives. Furthermore, buflavine was also prepared by using the p-p' diphenol coupling followed by dienone-phenol rearrangement as a key step. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2004.03.087
点击查看最新优质反应信息

文献信息

  • Synthesis of Amaryllidaceae alkaloids, siculine, oxocrinine, epicrinine, and buflavine
    作者:Sumiaki Kodama、Hirofumi Takita、Tetsuya Kajimoto、Kiyoharu Nishide、Manabu Node
    DOI:10.1016/j.tet.2004.03.087
    日期:2004.5
    Three crinane type of alkaloids isolated from Amaryllidaceae family were synthesized by taking advantage of the PIFA-mediated intramolecular p-p' diphenol coupling reaction of norbelladine derivatives. Furthermore, buflavine was also prepared by using the p-p' diphenol coupling followed by dienone-phenol rearrangement as a key step. (C) 2004 Elsevier Ltd. All rights reserved.
查看更多