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(3SR,4RS)-3-chloro-1-(trimethylsilyl)hept-5-en-1-yn-4-ol

中文名称
——
中文别名
——
英文名称
(3SR,4RS)-3-chloro-1-(trimethylsilyl)hept-5-en-1-yn-4-ol
英文别名
(E,3R,4S)-3-chloro-1-trimethylsilylhept-5-en-1-yn-4-ol
(3SR,4RS)-3-chloro-1-(trimethylsilyl)hept-5-en-1-yn-4-ol化学式
CAS
——
化学式
C10H17ClOSi
mdl
——
分子量
216.783
InChiKey
JQLRLZARLOFCAT-ROSGPLSXSA-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):
    2.41
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.6
  • 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:
    巴豆醛(3-chloro-1-propynyl)trimethylsilane 在 zinc dibromide 、 lithium diisopropyl amide 作用下, 以 四氢呋喃 为溶剂, 生成 (3RS,4RS)-3-chloro-1-(trimethylsilyl)hept-5-en-1-yn-4-ol 、 (3SR,4RS)-3-chloro-1-(trimethylsilyl)hept-5-en-1-yn-4-ol
    参考文献:
    名称:
    Propargylic Carbenoids 的制备和与羰基化合物的反应 - 炔丙基卤代醇和环氧乙烷的立体选择性合成
    摘要:
    描述了锌基丙二烯 3 的制备和反应性。这种有机金属化合物与醛反应生成具有良好非对映选择性的炔丙基卤代醇。这些卤代醇可以很容易地转化为炔丙基环氧乙烷。
    DOI:
    10.1002/1099-0690(200109)2001:17<3295::aid-ejoc3295>3.0.co;2-t
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文献信息

  • Metallotropic Equilibrium and Configurational Stability of 3-Chloro-1-(trimethylsilyl)propargyl and -allenyl Metals: Comparative Study among Lithium, Titanium, and Zinc
    作者:Joseph Bejjani、Candice Botuha、Fabrice Chemla、Franck Ferreira、Sarah Magnus、Alejandro Pérez-Luna
    DOI:10.1021/om300420q
    日期:2012.7.9
    A comparative study of the metallotropic equilibrium between 1-chloro-3-(trimethylsilyl)propargyl and -allenyl metals was undertaken by means of lithio-, titano-, and zinco-carbenoids. The lithium and zinc species were shown to react mainly in their allenic metallotropic forms, whereas the titanium species proved to react in both its propargylic and allenic forms. The configurational stability of these organometallics was next examined using a modification of the Hoffmann test. In each case, the organometallic was reacted with a chiral enantiopure electrophile. A comparison of the diastereomeric ratios obtained at low and high conversion rates of the reagent allows assessment of its configurational stability. The lithium species thus exhibited a configurational lability at -125 degrees C in Trapp mixture on the time scale of its reaction with (+)-camphor, while the titanium analogue proved to be configurationally stable at -40 degrees C in THF/Et2O on the time scale defined by its reaction with (S)-N-tritylprolinal. In the context of its reaction with the same electrophile, the zinc bromide species was proven to be partially labile from -80 degrees C in THF and its dynamic kinetic resolution was investigated.
  • Preparation of Propargylic Carbenoids and Reactions with Carbonyl Compounds − A Stereoselective Synthesis of Propargylic Halohydrins and Oxiranes
    作者:Fabrice Chemla、Nicolas Bernard、Franck Ferreira、Jean F. Normant
    DOI:10.1002/1099-0690(200109)2001:17<3295::aid-ejoc3295>3.0.co;2-t
    日期:2001.9
    The preparation and the reactivity of the zincioallene 3 is described. This organometallic compound reacts with aldehydes to yield propargylic halohydrins with good diastereoselectivities. These halohydrins can easily be converted into propargylic oxiranes.
    描述了锌基丙二烯 3 的制备和反应性。这种有机金属化合物与醛反应生成具有良好非对映选择性的炔丙基卤代醇。这些卤代醇可以很容易地转化为炔丙基环氧乙烷。
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