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(1R,3Z,5S)-1-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]heptadec-3-ene-1,5-diol | 619315-53-6

中文名称
——
中文别名
——
英文名称
(1R,3Z,5S)-1-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]heptadec-3-ene-1,5-diol
英文别名
(Z,1R,5S)-1-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]heptadec-3-ene-1,5-diol
(1R,3Z,5S)-1-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]heptadec-3-ene-1,5-diol化学式
CAS
619315-53-6
化学式
C22H42O4
mdl
——
分子量
370.573
InChiKey
LTBNBICGFMLTFD-CRKPHAGASA-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):
    6.1
  • 重原子数:
    26
  • 可旋转键数:
    15
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.91
  • 拓扑面积:
    58.9
  • 氢给体数:
    2
  • 氢受体数:
    4

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

反应信息

  • 作为反应物:
    描述:
    N-(苯硒基)邻苯二甲酰亚胺2,2-二甲氧基丙烷(1R,3Z,5S)-1-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]heptadec-3-ene-1,5-diol 在 camphor-10-sulfonic acid 作用下, 以 二氯甲烷 为溶剂, 反应 32.0h, 生成 (1R,2S)-1-[(2R,4R)-4-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]oxetan-2-yl]-1-phenylselanyltetradecan-2-ol 、 (1S,2S)-1-[(2R,4R)-4-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]oxetan-2-yl]-1-phenylselanyltetradecan-2-ol
    参考文献:
    名称:
    Electrophilic selenocyclization in 2-ene-1,5-diol systems: unexpected oxetane vs. tetrahydrofuran formation
    摘要:
    Electrophile-induced cyclization of (E)- and (Z)-2-ene-1,5-diols to tetrahydrofurans and oxetanes is described. Significant differences between the present report and previous work have been noted. A tentative model is proposed. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(03)01134-7
  • 作为产物:
    参考文献:
    名称:
    Electrophilic selenocyclization in 2-ene-1,5-diol systems: unexpected oxetane vs. tetrahydrofuran formation
    摘要:
    Electrophile-induced cyclization of (E)- and (Z)-2-ene-1,5-diols to tetrahydrofurans and oxetanes is described. Significant differences between the present report and previous work have been noted. A tentative model is proposed. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(03)01134-7
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文献信息

  • Electrophilic selenocyclization in 2-ene-1,5-diol systems: unexpected oxetane vs. tetrahydrofuran formation
    作者:Pierre Van de Weghe、Stéphane Bourg、Jacques Eustache
    DOI:10.1016/s0040-4020(03)01134-7
    日期:2003.9
    Electrophile-induced cyclization of (E)- and (Z)-2-ene-1,5-diols to tetrahydrofurans and oxetanes is described. Significant differences between the present report and previous work have been noted. A tentative model is proposed. (C) 2003 Elsevier Ltd. All rights reserved.
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