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(2R,4S)-2,4-dimethyl-5-oxo-6-phenylhexanoic acid | 1140504-75-1

中文名称
——
中文别名
——
英文名称
(2R,4S)-2,4-dimethyl-5-oxo-6-phenylhexanoic acid
英文别名
——
(2R,4S)-2,4-dimethyl-5-oxo-6-phenylhexanoic acid化学式
CAS
1140504-75-1
化学式
C14H18O3
mdl
——
分子量
234.295
InChiKey
XCYWTIWBHILTNT-WDEREUQCSA-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):
    2.5
  • 重原子数:
    17
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    54.4
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    (2R,4S)-2,4-dimethyl-5-oxo-6-phenylhexanoic acid三甲基硅烷化重氮甲烷甲醇乙醚 为溶剂, 生成 (-)-(2R,4S)-2,4-dimethyl-5-oxo-6-phenylhexanoic acid methyl ester
    参考文献:
    名称:
    Ligand differentiated complementary Rh-catalyst systems for the enantioselective desymmetrization of meso-cyclic anhydrides
    摘要:
    Two distinct systems for the rhodium-catalyzed enantioselective desymmetrization of meso-cyclic anhydrides have been developed. Each system has been optimized and are compatible with the use of in situ prepared organozinc reagents. Rhodium/PHOX species efficiently catalyze the addition of alkyi nucleophiles to glutaric anhydrides, while system is effective in the enantioselective arylation of succinic and glutaric anhydrides. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.10.075
  • 作为产物:
    描述:
    顺式-3,5-二甲基二氢-2H-吡喃-2,6(3H)-二酮苄基氯化镁 在 zinc diacetate 、 di-μ-chlorobis(norbornadiene)dirhodium(I)(S)-4-叔丁基-2-[2-(二苯基膦基)苯基]-2-噁唑啉 作用下, 以 四氢呋喃乙醚 为溶剂, 反应 1.5h, 以87%的产率得到(2R,4S)-2,4-dimethyl-5-oxo-6-phenylhexanoic acid
    参考文献:
    名称:
    3,5-二甲基戊二酸酐的对映体铑催化的烷基化不对称化
    摘要:
    铑催化的对映选择性的交叉偶联藻³已经开发,得到相应的产物,有机锌试剂和3,5-二甲基戊二酸酐顺-deoxypolypropionates,以优良产率和对映选择性。已经开发了该反应,以使得市售的和原位 制备的有机锌试剂均是有效的偶联伴侣。 有机锌试剂-格氏试剂-CC键形成-顺-脱氧聚丙烯酸酯
    DOI:
    10.1055/s-0028-1083275
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文献信息

  • Ligand differentiated complementary Rh-catalyst systems for the enantioselective desymmetrization of meso-cyclic anhydrides
    作者:Jeffrey B. Johnson、Matthew J. Cook、Tomislav Rovis
    DOI:10.1016/j.tet.2008.10.075
    日期:2009.4
    Two distinct systems for the rhodium-catalyzed enantioselective desymmetrization of meso-cyclic anhydrides have been developed. Each system has been optimized and are compatible with the use of in situ prepared organozinc reagents. Rhodium/PHOX species efficiently catalyze the addition of alkyi nucleophiles to glutaric anhydrides, while system is effective in the enantioselective arylation of succinic and glutaric anhydrides. (C) 2008 Elsevier Ltd. All rights reserved.
  • Enantioselective Rhodium-Catalyzed Alkylative Desymmetrization of 3,5-Dimethylglutaric Anhydride
    作者:Tomislav Rovis、Matthew Cook
    DOI:10.1055/s-0028-1083275
    日期:2009.1
    A rhodium-catalyzed enantioselective cross-coupling of sp³ organozinc reagents and 3,5-dimethylglutaric anhydride has been developed to afford the corresponding products, syn-deoxypolypropionates, in excellent yields and enantioselectivities. This reaction has been developed so that both commercially available and in situ prepared organozinc reagents are competent coupling partners. organozinc reagents
    铑催化的对映选择性的交叉偶联藻³已经开发,得到相应的产物,有机锌试剂和3,5-二甲基戊二酸酐顺-deoxypolypropionates,以优良产率和对映选择性。已经开发了该反应,以使得市售的和原位 制备的有机锌试剂均是有效的偶联伴侣。 有机锌试剂-格氏试剂-CC键形成-顺-脱氧聚丙烯酸酯
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