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diphenyl (naphthalen-1-yl(phenylamino)methyl)phosphine oxide | 102480-03-5

中文名称
——
中文别名
——
英文名称
diphenyl (naphthalen-1-yl(phenylamino)methyl)phosphine oxide
英文别名
-diphenyl-phosphinoxid
diphenyl (naphthalen-1-yl(phenylamino)methyl)phosphine oxide化学式
CAS
102480-03-5
化学式
C29H24NOP
mdl
——
分子量
433.489
InChiKey
RGKOJXDIAAAOFO-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

反应信息

  • 作为产物:
    描述:
    1-萘甲醛苯胺Diphenylphosphine oxide 在 silver hexafluoroantimonate 作用下, 以 neat (no solvent) 为溶剂, 反应 6.5h, 以80%的产率得到diphenyl (naphthalen-1-yl(phenylamino)methyl)phosphine oxide
    参考文献:
    名称:
    Silver‐Catalyzed One‐Pot Three‐Component Synthesis of α‐Aminonitriles and Biologically Relevant α‐Amino‐phosphonates
    摘要:
    AbstractA simple silver salt (AgSbF6)‐catalyzed aminophosphonylation and Strecker reaction have been developed and successfully applied to a wide range of substrates (>55 substrates). This solvent‐, ligand‐, and base‐free one‐pot three‐component protocol operates effectively at room temperature to provide diversified α‐aminophosphonates and α‐aminonitriles, which gave access to the respective α‐amino amides. Importantly, the present catalyst system is also capable to produce the rarely reported and biologically relevant aminophosphonates (having anti‐leishmanial activity). Further, mechanistic studies reveal that the present phosphonylation protocol follows a radical pathway.
    DOI:
    10.1002/asia.202200703
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