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(Z)-1-tosylazacyclohenicos-11-ene-2,21-dione | 1426264-58-5

中文名称
——
中文别名
——
英文名称
(Z)-1-tosylazacyclohenicos-11-ene-2,21-dione
英文别名
——
(Z)-1-tosylazacyclohenicos-11-ene-2,21-dione化学式
CAS
1426264-58-5
化学式
C27H41NO4S
mdl
——
分子量
475.693
InChiKey
QTWNHTGVSQVXQJ-IHWYPQMZSA-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):
    6.85
  • 重原子数:
    33.0
  • 可旋转键数:
    2.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.63
  • 拓扑面积:
    71.52
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

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

反应信息

  • 作为产物:
    描述:
    N-(4-methylphenyl)sulfonyl-N-undec-10-enoylundec-10-enamide 在 second-generation Hoveyda-Grubbs catalyst supported on mesocellular siliceous foam with nanopores(> 7nm) 作用下, 以 十二烷二氯甲烷 为溶剂, 反应 6.0h, 以35.484%的产率得到
    参考文献:
    名称:
    Highly Selective Macrocycle Formations by Metathesis Catalysts Fixated in Nanopores
    摘要:
    Ruthenium-based metathesis catalysts immobilized on mesocellular siliceous foam (MCF) bearing large nanopores proved highly efficient and selective for macrocyclic ring-closing metathesis (RCM). Kinetic studies revealed that the homogeneous counterpart exhibited far higher activity that accounted for more oligomerization pathways and resulted in less macrocyclization products. Meanwhile, the immobilized catalysts showed lower conversion rates leading to higher yields of macrocyclic products in a given reaction time, with conversion rates and yields dependent upon pore size, catalyst loading density, and linker length. The macrocycle formations via RCM were accelerated by increasing the pore size and decreasing the catalyst loading density while retaining the comparably high yield. The catalysts immobilized on MCF, of which silica surface is rigid and pores are relatively large, showed high conversion rates and yields compared with an analogue immobilized on TentaGel resins, of which backbone becomes flexible upon swelling in the reaction medium. It is noteworthy that the selectivity for the macrocyclic RCM can be significantly improved by tuning the catalyst initiation rates via immobilization onto the support materials in which well-defined three-dimentional network of large nanopores are deployed.
    DOI:
    10.1021/jo302823w
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