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(Z)-14-(tributylstannyl)tetradeca-1,13-dien-4-ol | 1599432-58-2

中文名称
——
中文别名
——
英文名称
(Z)-14-(tributylstannyl)tetradeca-1,13-dien-4-ol
英文别名
——
(Z)-14-(tributylstannyl)tetradeca-1,13-dien-4-ol化学式
CAS
1599432-58-2
化学式
C26H52OSn
mdl
——
分子量
499.408
InChiKey
IXVXVKXKZOYKAA-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):
    8.51
  • 重原子数:
    28
  • 可旋转键数:
    14
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    A One-Pot Allylation–Hydrostannation Sequence with Recycling of the Intermediate Tin Waste
    摘要:
    A one-pot allylation and hydrostannation of alkynals where the tin byproduct formed in the first step of the reaction is recycled and used in the second step of the sequence is presented. Specifically, a BF3 center dot OEt2-promoted allylstannation of the aldehyde moiety in the alkynalis followed by the introduction of polymethylhydrosiloxane (PMHS) and catalytic B(C6F5)(3), which convert the tin byproduct of the allylation into Bu3SnH, which then hydrostannates the alkyne in the molecule. Sn-119 and B-11 NMR data suggest an organotin fluoride species is formed during the allylation step and involved in the tin recycling step.
    DOI:
    10.1021/ol500460u
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文献信息

  • A One-Pot Allylation–Hydrostannation Sequence with Recycling of the Intermediate Tin Waste
    作者:Banibrata Ghosh、Maria Del Rosario I. Amado-Sierra、Daniel Holmes、Robert E. Maleczka
    DOI:10.1021/ol500460u
    日期:2014.5.2
    A one-pot allylation and hydrostannation of alkynals where the tin byproduct formed in the first step of the reaction is recycled and used in the second step of the sequence is presented. Specifically, a BF3 center dot OEt2-promoted allylstannation of the aldehyde moiety in the alkynalis followed by the introduction of polymethylhydrosiloxane (PMHS) and catalytic B(C6F5)(3), which convert the tin byproduct of the allylation into Bu3SnH, which then hydrostannates the alkyne in the molecule. Sn-119 and B-11 NMR data suggest an organotin fluoride species is formed during the allylation step and involved in the tin recycling step.
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