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Diazo-acetic acid 10-(2-diazo-acetoxy)-decyl ester | 7215-40-9

中文名称
——
中文别名
——
英文名称
Diazo-acetic acid 10-(2-diazo-acetoxy)-decyl ester
英文别名
10-(2-Diazoacetyl)oxydecyl 2-diazoacetate
Diazo-acetic acid 10-(2-diazo-acetoxy)-decyl ester化学式
CAS
7215-40-9
化学式
C14H22N4O4
mdl
——
分子量
310.353
InChiKey
DEASXLLFCROKSP-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):
    4.1
  • 重原子数:
    22
  • 可旋转键数:
    15
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    56.6
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    Diazo-acetic acid 10-(2-diazo-acetoxy)-decyl ester 在 [Ru(2,6-Cl2tpp)CO] 作用下, 以 1,2-二氯乙烷 为溶剂, 反应 21.0h, 以66%的产率得到(Z)-1,6-Dioxa-cyclohexadec-3-ene-2,5-dione
    参考文献:
    名称:
    Highly Selective Intra- and Intermolecular Coupling Reactions of Diazo Compounds to Form cis-Alkenes Using a Ruthenium Porphyrin Catalyst
    摘要:
    [Ru(2,6-Cl2TPP)(CO)] catalyzed intramolecular coupling reactions of bisdiazoacetates and intermolecular coupling reactions of monodiazoacetates to afford the coupling products in up to 76% and 93% yields, respectively. Only the cis isomers were obtained from the reactions. Employing such a ruthenium-catalyzed coupling reaction of a diazo compound as a key step allowed the synthesis of Patulolide B in 67% yield with a ratio of >40:1 against its trans isomer.
    DOI:
    10.1021/ol049626a
  • 作为产物:
    描述:
    参考文献:
    名称:
    Highly Selective Intra- and Intermolecular Coupling Reactions of Diazo Compounds to Form cis-Alkenes Using a Ruthenium Porphyrin Catalyst
    摘要:
    [Ru(2,6-Cl2TPP)(CO)] catalyzed intramolecular coupling reactions of bisdiazoacetates and intermolecular coupling reactions of monodiazoacetates to afford the coupling products in up to 76% and 93% yields, respectively. Only the cis isomers were obtained from the reactions. Employing such a ruthenium-catalyzed coupling reaction of a diazo compound as a key step allowed the synthesis of Patulolide B in 67% yield with a ratio of >40:1 against its trans isomer.
    DOI:
    10.1021/ol049626a
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文献信息

  • Gold-catalyzed intramolecular diazo coupling: an efficient macrocyclization towards cyclic olefins
    作者:Chenghao Zhu、Guangyang Xu、Kai Liu、Lin Qiu、Shiyong Peng、Jiangtao Sun
    DOI:10.1039/c5cc04830c
    日期:——

    A gold-catalyzed synthesis of medium to large membered cyclic olefins has been developed.

    一种利用金催化的合成中等到大环烯烃的方法已经开发出来了。
  • US5376712A
    申请人:——
    公开号:US5376712A
    公开(公告)日:1994-12-27
  • Highly Selective Intra- and Intermolecular Coupling Reactions of Diazo Compounds to Form <i>cis</i>-Alkenes Using a Ruthenium Porphyrin Catalyst
    作者:Gong-Yong Li、Chi-Ming Che
    DOI:10.1021/ol049626a
    日期:2004.5.1
    [Ru(2,6-Cl2TPP)(CO)] catalyzed intramolecular coupling reactions of bisdiazoacetates and intermolecular coupling reactions of monodiazoacetates to afford the coupling products in up to 76% and 93% yields, respectively. Only the cis isomers were obtained from the reactions. Employing such a ruthenium-catalyzed coupling reaction of a diazo compound as a key step allowed the synthesis of Patulolide B in 67% yield with a ratio of >40:1 against its trans isomer.
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