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[2-methoxy-6-[(1S)-1-methylsulfanylethyl]phenyl] selenohypobromite | 819852-45-4

中文名称
——
中文别名
——
英文名称
[2-methoxy-6-[(1S)-1-methylsulfanylethyl]phenyl] selenohypobromite
英文别名
——
[2-methoxy-6-[(1S)-1-methylsulfanylethyl]phenyl] selenohypobromite化学式
CAS
819852-45-4
化学式
C10H13BrOSSe
mdl
——
分子量
340.143
InChiKey
XKIZCSBMBODUQK-ZETCQYMHSA-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

物化性质

  • 沸点:
    373.1±42.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.76
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    34.5
  • 氢给体数:
    0
  • 氢受体数:
    2

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:
    [2-methoxy-6-[(1S)-1-methylsulfanylethyl]phenyl] selenohypobromite甲醇二氯甲烷 为溶剂, 反应 12.0h, 生成 (S)-1-Methoxy-2-[2-methoxy-6-((S)-1-methylsulfanyl-ethyl)-phenylselanyl]-heptan-3-ol
    参考文献:
    名称:
    Kinetic Resolution of Allylic Alcohols Promoted by Electrophilic Selenium Reagents
    摘要:
    The first example of a kinetic resolution process promoted by an electrophilic selenium reagent is reported. Racemic allylic alcohols react with half equivalents of a selenenylating agent in methanol leading to the regiospecific formation, of the corresponding addition products with a very high level of facial selectivity (98% de). The unreacted alcohol can be recovered in a optically enriched form (92% ee).
    DOI:
    10.1080/10426500590906355
  • 作为产物:
    描述:
    bis[2-methoxy-6-[(1S)-1-(methythio)ethyl]phenyl]diselenide 在 作用下, 以 乙醚 为溶剂, 生成 [2-methoxy-6-[(1S)-1-methylsulfanylethyl]phenyl] selenohypobromite
    参考文献:
    名称:
    Kinetic Resolution of Allylic Alcohols Promoted by Electrophilic Selenium Reagents
    摘要:
    The first example of a kinetic resolution process promoted by an electrophilic selenium reagent is reported. Racemic allylic alcohols react with half equivalents of a selenenylating agent in methanol leading to the regiospecific formation, of the corresponding addition products with a very high level of facial selectivity (98% de). The unreacted alcohol can be recovered in a optically enriched form (92% ee).
    DOI:
    10.1080/10426500590906355
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文献信息

  • A Chiral Electrophilic Selenium Reagent To Promote the Kinetic Resolution of Racemic Allylic Alcohols
    作者:Marcello Tiecco、Lorenzo Testaferri、Claudio Santi、Cristina Tomassini、Rosaria Bonini、Francesca Marini、Luana Bagnoli、Andrea Temperini
    DOI:10.1021/ol048001+
    日期:2004.12.1
    [reaction: see text] The first example of a kinetic resolution process promoted by electrophilic selenium reagents is reported. Racemic allylic alcohols react with half equivalents of a selenenylating agent in methanol leading to the regiospecific formation of the corresponding addition products with a very high level of facial selectivity (from 95:5 to 98:2 dr). The unreacted alcohols can be recovered
    [反应:见正文]报告了由亲电子硒试剂促进的动力学拆分过程的第一个例子。外消旋烯丙醇与甲醇中半当量的硒烯化剂反应,导致具有非常高的面部选择性(从95:5至98:2 dr)的相应加成产物区域特异性形成。未反应的醇可以光学富集的形式(从90%到94%ee)回收。
  • Kinetic Resolution of Allylic Alcohols Promoted by Electrophilic Selenium Reagents
    作者:C. Santi、M. Tiecco、L. Testaferri、C. Tomassini、F. Marini、L. Bagnoli、A. Temperini
    DOI:10.1080/10426500590906355
    日期:2005.2.23
    The first example of a kinetic resolution process promoted by an electrophilic selenium reagent is reported. Racemic allylic alcohols react with half equivalents of a selenenylating agent in methanol leading to the regiospecific formation, of the corresponding addition products with a very high level of facial selectivity (98% de). The unreacted alcohol can be recovered in a optically enriched form (92% ee).
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