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(4-(benzyloxy)-7-(((tert-butyldimethylsilyl)oxy)methyl)-5-methoxynaphthalen-1-yl)boronic acid | 1248682-83-8

中文名称
——
中文别名
——
英文名称
(4-(benzyloxy)-7-(((tert-butyldimethylsilyl)oxy)methyl)-5-methoxynaphthalen-1-yl)boronic acid
英文别名
——
(4-(benzyloxy)-7-(((tert-butyldimethylsilyl)oxy)methyl)-5-methoxynaphthalen-1-yl)boronic acid化学式
CAS
1248682-83-8
化学式
C25H33BO5Si
mdl
——
分子量
452.431
InChiKey
NUQLXGXWRUXSEZ-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):
    4.63
  • 重原子数:
    32.0
  • 可旋转键数:
    8.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    68.15
  • 氢给体数:
    2.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    ((1R,3S)-5-iodo-6,8-dimethoxy-1-methyl-2-tosyl-1,2,3,4-tetrahydroisoquinolin-3-yl)methyl acetate 、 (4-(benzyloxy)-7-(((tert-butyldimethylsilyl)oxy)methyl)-5-methoxynaphthalen-1-yl)boronic acid2-双环己基膦-2',6'-二甲氧基联苯potassium phosphate 、 palladium diacetate 作用下, 以 正丁醇 为溶剂, 反应 24.0h, 生成 ((1R,3S)-5-(4-(benzyloxy)-7-(((tert-butyldimethylsilyl)oxy)methyl)-5-methoxynaphthalen-1-yl)-6,8-dimethoxy-1-methyl-2-tosyl-1,2,3,4-tetrahydroisoquinolin-3-yl)methyl acetate
    参考文献:
    名称:
    Total Synthesis of (+)-Korupensamine B via an Atropselective Intermolecular Biaryl Coupling
    摘要:
    The asymmetric total synthesis of nonracemic korupensamine B is reported. It includes a newly designed and highly trans-diastereoselective (>20:1 dr) route to the tetrahydroisoquinoline ring and an unprecedented atropdiastereoselective Suzuki-Miyaura coupling for construction of the fully fashioned naphthylisoquinoline framework that invokes pi stacking as a possible source of stereocontrol.
    DOI:
    10.1021/ja1065202
  • 作为产物:
    参考文献:
    名称:
    Total Synthesis of (+)-Korupensamine B via an Atropselective Intermolecular Biaryl Coupling
    摘要:
    The asymmetric total synthesis of nonracemic korupensamine B is reported. It includes a newly designed and highly trans-diastereoselective (>20:1 dr) route to the tetrahydroisoquinoline ring and an unprecedented atropdiastereoselective Suzuki-Miyaura coupling for construction of the fully fashioned naphthylisoquinoline framework that invokes pi stacking as a possible source of stereocontrol.
    DOI:
    10.1021/ja1065202
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