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(E)-2-hexenal cyanohydrin ethyl carbonate

中文名称
——
中文别名
——
英文名称
(E)-2-hexenal cyanohydrin ethyl carbonate
英文别名
[(E)-1-cyanohex-2-enyl] ethyl carbonate
(E)-2-hexenal cyanohydrin ethyl carbonate化学式
CAS
——
化学式
C10H15NO3
mdl
——
分子量
197.234
InChiKey
ZQVUCNDJGAVURK-VOTSOKGWSA-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):
    2.7
  • 重原子数:
    14
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    59.3
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

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文献信息

  • Construction of Highly Functional Quaternary Carbon Stereocenters <i>via</i> an Organocatalytic Tandem Cyanation–Allylic Alkylation Reaction
    作者:Zhe Zhuang、Feng Pan、Jian-Guo Fu、Jian-Ming Chen、Wei-Wei Liao
    DOI:10.1021/ol202499g
    日期:2011.12.2
    The first tertiary amine-catalyzed tandem cyanation-allyic alkylation (CAA) reaction of aldehydes, appropriate cyanide sources, and Morita-Baylis-Hillman (MBH) adducts has been developed, which provides a facile access to densely functionalized products containing O-substituted quaternary centers.
  • Lewis Base Promoted Intramolecular Acylcyanation of α-Substituted Activated Alkenes: Construction of Ketones Bearing β-Quaternary Carbon Centers
    作者:Zhe Zhuang、Jian-Ming Chen、Feng Pan、Wei-Wei Liao
    DOI:10.1021/ol3007716
    日期:2012.5.4
    A novel phosphine-promoted intramolecular acylcyanation of alpha-substituted activated alkenes has been developed, which provides a unique access to densely functionalized acyclic ketones bearing beta-quaternary carbon centers with a remarkable feature that both alpha- and beta-positions of activated alkene are functionalized.
  • A Two-Step Procedure for the Conversion of <i>α,β</i>-Unsaturated Aldehydes into <i>γ</i><i>-</i>Azido-<i>α,β</i>-Unsaturated Nitriles<sup>1</sup>
    作者:Donald R. Deardorff、Cullen M. Taniguchi、Sanaz A. Tafti、Henry Y. Kim、So Young Choi、Katherine J. Downey、Thanh V. Nguyen
    DOI:10.1021/jo010101v
    日期:2001.10.1
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