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(propiophenone)Cr(CO)3 | 58535-55-0

中文名称
——
中文别名
——
英文名称
(propiophenone)Cr(CO)3
英文别名
tricarbonyl(η6-propiophenone)chromium;tricarbonyl[(η(6)-phenyl)-1-propanone]chromium;carbon monoxide;chromium;1-phenylpropan-1-one
(propiophenone)Cr(CO)3化学式
CAS
58535-55-0
化学式
C12H10CrO4
mdl
——
分子量
270.205
InChiKey
ROLVZGWGJPFAEY-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    描述:
    (propiophenone)Cr(CO)3葡萄糖 、 yeast 作用下, 以 乙醇 为溶剂, 以20%的产率得到(1-phenylpropanol)Cr(CO)3
    参考文献:
    名称:
    对映体还原过渡金属络合芳族酮的微生物
    摘要:
    面包酵母还原Cr(CO 3)络合的芳香酮的几个例子表明,在某些情况下,这种方法可以提高还原速度,增加对映体过量,甚至可以动力学拆分平面手性络合物。
    DOI:
    10.1039/c39880001224
  • 作为产物:
    描述:
    tricarbonyl[2-ethyl-2-(η(6)-phenyl)-1,3-dioxolane]chromium 在 p-toluenesulphonic acid 作用下, 以 丙酮 为溶剂, 以89%的产率得到(propiophenone)Cr(CO)3
    参考文献:
    名称:
    Synthesis and reactions of [(((η6)-2-acylaryl)-C,O)tetracarbonylmanganese]-tricarbonylchromium complexes: enhancement of diastereoselection during cyclopentaannulation
    摘要:
    Cyclomanganation reactions of [(eta(6))-acylaryl]tricarbonylchromium complexes have been investigated, Three novel heterobimetallic complexes have been synthesised in moderate to good yield, with one being characterised by X-ray crystallography. Several modes of activating these bimetallic complexes towards coupling reactions with substituted alkenes and alkynes were investigated, including oxidative decarbonylation at room temperature, and thermal promotion. The stereochemistry of one of the cyclopentaannulated adducts has been established by X-ray crystallography. Thermal displacement of one of the CO ligands of the bimetallic complex 27 in the presence of PPh(3) afforded a single adduct, the structure of which was established by X-ray crystallography. The chemistry of this novel bimetallic system was investigated.
    DOI:
    10.1016/0022-328x(95)05964-q
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文献信息

  • Ruthenium-catalyzed reduction of racemic tricarbonyl(η6-aryl ketone)chromium complexes using transfer hydrogenation: A simple alternative to the resolution of planar chiral organometallics
    作者:Cleber V. Ursini、Gilson H.M. Dias、J. Augusto R. Rodrigues
    DOI:10.1016/j.jorganchem.2005.03.048
    日期:2005.7
    resulted in optically active syn-(R,S)-(η6-aryl alcohol)Cr(CO)3 and (R)-(η6-aryl ketone)Cr(CO)3 compounds in 31–97% ee. Reduction of racemic (η6-thiochroman-4-one)Cr(CO)3 with the catalyst precursor generated from (+)-norephedrine, instead of ()-ephedrine, inverted the configuration of the products obtained. Syn-(S,R)-(η6-thiochroman-4-ol)Cr(CO)3 and (S)-(η6-thiochroman-4-one)-Cr(CO)3 were isolated
    外消旋平面手性(η 6 -芳基酮)的Cr(CO)3个配合物(芳基酮= -1-二氢酮,1-四氢酮,4-苯并二氢吡喃酮和二氢苯并噻喃-4-酮)通过回流以Cr(CO)芳基酮制备在二丁醚和THF的10∶1混合物中得到6。有机属酮的通过转移氢化在含有KOH和催化剂前体的2-丙醇的减少,从将[RuCl产生2(η 6 -苯)] 2( - ) -麻黄碱,导致光学活性和顺- ([R ,小号) - (η 6 -芳基醇)的Cr(CO)3和(- [R )- (η 6 -芳基酮)的Cr(CO)在31–97%ee中包含3种化合物。外消旋的减少(η 6二氢苯并噻喃-4-酮)的Cr(CO)3与来自(+)所产生的催化剂前体-降麻黄碱代替( - ) -麻黄碱,反相获得的产物的结构。顺式- (小号,- [R )- (η 6二氢苯并噻喃-4-醇)的Cr(CO)3和(小号) - (η 6二氢苯并噻喃-4-酮)-Cr(CO)3分离的ee分别为49%和>
  • Card, Annie; Besancon, Jack; Gautheron, Bernard, Bulletin de la Societe Chimique de France, 1981, vol. II, p. 43 - 50
    作者:Card, Annie、Besancon, Jack、Gautheron, Bernard
    DOI:——
    日期:——
  • Synthèse asymétrique d'alcools benchrotréniques par voie microbiologique
    作者:Jeannine Gillois、Gérard Jaouen、Didier Buisson、Robert Azerad
    DOI:10.1016/0022-328x(89)87209-2
    日期:1989.5
  • Synthesis of isomeric benchrotrenic alkenes by Ti-induced carbonyl coupling reaction
    作者:J. Besançon、J. Szymoniak、C. Moïse
    DOI:10.1016/0022-328x(92)83065-p
    日期:1992.3
    The benchrotrenic ketones BctCOR (1) (Bct: Cr(CO)3C6H5; R = CH3 (a), C2H5 (b), n-C3H7 (c), n-C4H9 (d)) undergo reductive alkene coupling reaction when treated with TiCl3/Li. The two isomeric forms of Bct(R)C=C(R)Bct (2) were isolated in the ratio Z/E = ca. 3:1. Decomplexation of 2 by iodine gave quantitatively the corresponding isomeric alkyl stilbenes C6H5(R)C=C(R)C6H5 (3).
  • GILLOIS, JEANNINE;JAOUEN, GERARD;BUISSON, DIDIER;AZERAD, ROBERT, J. ORGANOMET. CHEM., 367,(1989) N-2, C. 85-93
    作者:GILLOIS, JEANNINE、JAOUEN, GERARD、BUISSON, DIDIER、AZERAD, ROBERT
    DOI:——
    日期:——
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