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| 215777-60-9

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
215777-60-9
化学式
C29H23CrNO4
mdl
——
分子量
501.502
InChiKey
JSJPYEIBOMAPFM-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:
    (CO)5CrC(C6H5)N(CH3)C3H5二苯基乙炔环己烷 为溶剂, 生成
    参考文献:
    名称:
    炔烃和一氧化碳插入铬的氨基碳烯络合物中获得的氮的合成,X射线结构和重排
    摘要:
    氨基碳烯络合物(CO)5 Cr C(R 1)N(R 2 R 3)1 [R 1 = H,Me,Ph,R 2 = Me,R 2 R 3 =(CH 2)5,R 3 = Me,环丙基]与二苯乙炔反应,得到氮的叶立德5,其在5a [[(CO)3 CrR 2 R 3 N(C 16 H 10 OR 1)–(R 1 = H ,R 2= R 3=(CH 2)5 ],并且在氮从烷基R 2和R 3迁移至碳时,其导致预期的内酰胺(例如8和9)C 16 H 10 ONR 1 R 2 R 3。
    DOI:
    10.1039/c39910001075
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文献信息

  • Reaction of aminocarbene complexes of chromium with alkynes. 1. Formation and rearrangement of ketene and nitrogen ylide complexes
    作者:Evelyne Chelain、Regis Goumont、Louis Hamon、Andree Parlier、Michele Rudler、Henri Rudler、Jean Claude Daran、Jacqueline Vaissermann
    DOI:10.1021/ja00047a018
    日期:1992.10
    The title reactions of chromium-containing carbene complexes (CO)5Cr=C(R1)N(R2R3) (R1 = H, Me, Ph; R2 = Me; R3 = Me, C3H5, CH2C3H5; R2R3 = (CH2)5) 8 and (CO)5Cr=C[(CH2)3C=CPh]N(R1R2) (R1 = R2 = Me; R1R2 = (CH2)5; R1R2 = (CH2)4) 9, bearing alkyl groups of low migratory aptitude on nitrogen, have been examined. In contrast to complexes in which nitrogen bears either an alkyl and an allyl or a benzyl group or is part of a strained cycle, which give heterocycles upon alkyne/CO insertions followed by nitrogen-to-carbon migrations (e.g., 1 --> 7), complexes 8 and 9 lead to stable nitrogen ylides, which could be fully characterized by X-ray crystallography in the case of 8a and 9a. Moreover, in the case of complexes of the general structure 9, ketene precursors of the ylides could either be detected (R1 = Me; R2 = CH2Ph) or isolated and characterized (R2R3 = (CH2)5). The new ylide complexes undergo, upon moderate heating, Stevens-type rearrangements to the expected heterocyclic compounds as a result of nitrogen-to-carbon migrations of various alkyl groups, and upon treatment with dimethyldioxirane, they undergo oxidation to lactone complexes.
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