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(2E,4Z,6E)-methyl 6-formyl-3-methyl-7-phenylhepta-2,4,6-trienoate | 1355676-74-2

中文名称
——
中文别名
——
英文名称
(2E,4Z,6E)-methyl 6-formyl-3-methyl-7-phenylhepta-2,4,6-trienoate
英文别名
——
(2E,4Z,6E)-methyl 6-formyl-3-methyl-7-phenylhepta-2,4,6-trienoate化学式
CAS
1355676-74-2
化学式
C16H16O3
mdl
——
分子量
256.301
InChiKey
PCXZLMDHNTWONN-MJRCHRDQSA-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):
    2.94
  • 重原子数:
    19.0
  • 可旋转键数:
    5.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    43.37
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Highly Enantioselective Cyclizations of Conjugated Trienes with Low Catalyst Loadings: A Robust Chiral N-Heterocyclic Carbene Enabled by Acetic Acid Cocatalyst
    摘要:
    Densely functionalized cyclopentenones are useful synthetic intermediates. We report herein a new method to synthesize this important class of compounds through a highly enantioselective (98 -> 99% ee) triene cyclization that is cocatalyzed by acetic acid and a chiral N-heterocyclic carbene (NHC). We discovered that acetic acid not only could coexist with NHCs but also could greatly stabilize the active catalyst, which enables a long-lived catalyst with high reactivity and selectivity.
    DOI:
    10.1021/ol203375y
  • 作为产物:
    描述:
    盐酸 作用下, 以 乙腈 为溶剂, 反应 0.17h, 以146 mg的产率得到(2E,4Z,6E)-methyl 6-formyl-3-methyl-7-phenylhepta-2,4,6-trienoate
    参考文献:
    名称:
    Highly Enantioselective Cyclizations of Conjugated Trienes with Low Catalyst Loadings: A Robust Chiral N-Heterocyclic Carbene Enabled by Acetic Acid Cocatalyst
    摘要:
    Densely functionalized cyclopentenones are useful synthetic intermediates. We report herein a new method to synthesize this important class of compounds through a highly enantioselective (98 -> 99% ee) triene cyclization that is cocatalyzed by acetic acid and a chiral N-heterocyclic carbene (NHC). We discovered that acetic acid not only could coexist with NHCs but also could greatly stabilize the active catalyst, which enables a long-lived catalyst with high reactivity and selectivity.
    DOI:
    10.1021/ol203375y
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