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3-(naphth-2-yl)-2-butenoic acid chloride | 1447519-96-1

中文名称
——
中文别名
——
英文名称
3-(naphth-2-yl)-2-butenoic acid chloride
英文别名
2-Butenoyl chloride, 3-(2-naphthalenyl)-, (2E)-;3-naphthalen-2-ylbut-2-enoyl chloride
3-(naphth-2-yl)-2-butenoic acid chloride化学式
CAS
1447519-96-1
化学式
C14H11ClO
mdl
——
分子量
230.694
InChiKey
DBZSKMGYRKKNEZ-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):
    4.7
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    3-(naphth-2-yl)-2-butenoic acid chloride2-(1-benzyl-2-oxo-1,2-dihydro-indol-3-ylidene)malononitrilecaesium carbonate三乙胺1,3-双(2,6-二异丙基苯基)氯化咪唑鎓 作用下, 以 四氢呋喃 为溶剂, 以62%的产率得到1'-benzyl-4-(naphthalen-2-yl)-2,2'-dioxospiro[cyclohex[3]ene-1,3'-indoline]-6,6-dicarbonitrile
    参考文献:
    名称:
    N-Heterocyclic Carbene-Catalyzed All Carbon-[4+2] Cyclocondensation ofα,β-Unsaturated Acyl Chlorides with 3-Alkylenyloxindoles
    摘要:
    AbstractAlthough the NHC‐catalyzed cyclization reactions have been well established for the synthesis of various heterocycles, the corresponding all carbon cyclization reaction for the synthesis of carbocycles is far less established. In this note, the NHC‐catalyzed all carbon [4+2] cyclocondensation of α,β‐unsaturated acyl chlorides and 3‐alkenyloxindoles was developed to give the corresponding spirocarbocyclic oxindoles in good yield with good to high diastereoselectivities.
    DOI:
    10.1002/cjoc.201400411
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文献信息

  • [EN] TELOMERASE REVERSE TRANSCRIPTASE DEGRADERS AND METHODS OF USE THEREOF<br/>[FR] AGENTS DE DÉGRADATION DE LA TRANSCRIPTASE INVERSE DE LA TÉLOMÉRASE ET LEURS PROCÉDÉS D'UTILISATION
    申请人:WISTAR INST
    公开号:WO2020252195A1
    公开(公告)日:2020-12-17
    The present disclosure provides TERT inhibitor compounds, a TERT inhibitor linked to a ubiquitin ligase ligand, as well as pharmaceutical compositions thereof. The present disclosure also provides methods of inhibiting telomerase reverse transcriptase (TERT) and methods of treating or preventing a disease or disorder using said compounds and/or compositions.
    本公开提供了TERT抑制剂化合物,一个与泛素连接酶配体相关的TERT抑制剂,以及其药物组成物。本公开还提供了通过使用上述化合物和/或组成物来抑制端粒酶逆转录酶(TERT)的方法,以及治疗或预防疾病或紊乱的方法。
  • Catalytic [4+2] Cyclization of α,β-Unsaturated Acyl Chlorides with 3-Alkylenyloxindoles: Highly Diastereo- and Enantioselective Synthesis of Spirocarbocyclic Oxindoles
    作者:Li-Tao Shen、Wen-Qiang Jia、Song Ye
    DOI:10.1002/anie.201207405
    日期:2013.1.7
    Cinchona alkaloids were used as Lewis base catalysts in the title reaction. The [4+2] cyclization of α,β‐unsaturated acyl chlorides with electron‐deficient alkenes derived from oxindole gave the corresponding spirocarbocyclic oxindoles.
    金鸡纳生物碱在标题反应中用作路易斯碱催化剂。α,β-不饱和酰氯与衍生自氧吲哚的缺电子烯烃的环化[4 + 2]得到了相应的螺碳环羰基吲哚。
  • Organocatalytic [4 + 2] cyclocondensation of α,β-unsaturated acyl chlorides with imines: highly enantioselective synthesis of dihydropyridinone and piperidine derivatives
    作者:Wen-Qiang Jia、Xiang-Yu Chen、Li-Hui Sun、Song Ye
    DOI:10.1039/c4ob00114a
    日期:——
    alkaloid-catalyzed [4 + 2] cyclocondensation of α,β-unsaturated acyl chlorides with imines is developed to give the corresponding substituted dihydropyridinones in good yields with high to excellent enantioselectivities. Reduction of the dihydropyridinones gave highly optically active substituted tetrahydropyridinone and piperidine derivatives.
    开发了金鸡纳生物碱催化的亚胺与α,β-不饱和酰氯的[4 + 2]环缩合反应,可以以高收率和高至优异的对映选择性提供相应的取代二氢吡啶并酮。二氢吡啶酮的还原得到高度旋光的取代的四氢吡啶酮和哌啶衍生物。
  • <i>N</i>-Heterocyclic Carbene-Catalyzed All Carbon-[4+2] Cyclocondensation of<i>α</i>,<i>β</i>-Unsaturated Acyl Chlorides with 3-Alkylenyloxindoles
    作者:Litao Shen、Wenqiang Jia、Song Ye
    DOI:10.1002/cjoc.201400411
    日期:2014.8
    AbstractAlthough the NHC‐catalyzed cyclization reactions have been well established for the synthesis of various heterocycles, the corresponding all carbon cyclization reaction for the synthesis of carbocycles is far less established. In this note, the NHC‐catalyzed all carbon [4+2] cyclocondensation of α,β‐unsaturated acyl chlorides and 3‐alkenyloxindoles was developed to give the corresponding spirocarbocyclic oxindoles in good yield with good to high diastereoselectivities.
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