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3-benzofuran-3-yl-propenal | 1006591-55-4

中文名称
——
中文别名
——
英文名称
3-benzofuran-3-yl-propenal
英文别名
(E)-3-(benzofuran-3-yl)acrylaldehyde;(E)-3-benzofuran-3-ylpropenal;(E)-3-(1-benzofuran-3-yl)prop-2-enal
3-benzofuran-3-yl-propenal化学式
CAS
1006591-55-4
化学式
C11H8O2
mdl
——
分子量
172.183
InChiKey
KZCMXDVRTQHTEE-ONEGZZNKSA-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):
    2.2
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    30.2
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    3-benzofuran-3-yl-propenal 在 Tp(CF3)2Ag(thf) 、 sodium hydride 作用下, 以 甲醇二氯甲烷 、 mineral oil 为溶剂, 反应 18.0h, 生成
    参考文献:
    名称:
    烷烃的位点选择性 C−H 烯丙基化:轻松获得烯丙基季 sp3-碳中心
    摘要:
    未活化烷烃与非受体乙烯基卡宾的第一个位点选择性 C(sp 3 )−H 插入是通过银催化实现的,并以实验室稳定的乙烯基-N-三氟甲磺酰腙为底物。相应的产物具有烯丙基季sp 3 -碳中心并且以高产率获得。
    DOI:
    10.1002/anie.202214519
  • 作为产物:
    描述:
    2-bromophenyl 2-furylmethyl ether四(三苯基膦)钯potassium carbonate三苯基膦 作用下, 以 1,4-二氧六环 为溶剂, 反应 24.0h, 以55%的产率得到3-benzofuran-3-yl-propenal
    参考文献:
    名称:
    A Novel Entry to Functionalized Benzofurans and Indoles via Palladium(0)-Catalyzed Arylative Dearomatization of Furans
    摘要:
    A novel entry to functionalized benzofurans and indoles from furans in moderate to good yields has been developed. This protocol involves palladium(0)-catalyzed dearomatizing intramolecular arylation of the furan ring, formation of a pi-allylic palladium complex, furan ring opening, and a beta-hydride elimination sequence.
    DOI:
    10.1021/ol300008d
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文献信息

  • Scandium triflate and secondary amine promoted AA′B 2:1 coupling and formal inverse electron demand Diels–Alder reactions of dienals
    作者:Chris D. Smith、Robert A. Batey
    DOI:10.1016/j.tet.2007.11.035
    日期:2008.1
    ion activation of the diene. A purely amine promoted formal inverse electron demand Diels–Alder cycloaddition approach was also demonstrated in the 2:1 coupling of 2,4-hexadienal with methanol. These reactions demonstrate the concepts of dual metal/amine catalysis and amine promoted formal inverse electron demand Diels–Alder cycloadditions. They differ from known examples of organocatalyzed Diels–Alder
    反应前瞻性研究导致发现Sc(OTf)3促进了咪唑苯并呋喃取代的醛与吗啉的新型AA'B 2:1偶联。相关的Sc(OTf)3证明了吗啉促进的反应用于苯并呋喃取代的醛与二呋喃的偶联。这些加合物的形成与形式上的逆电子需求Diels-Alder环加成相一致,最有可能通过逐步发生的多米诺米歇尔-曼尼希(Domino Michael-Mannich)环化过程,涉及二亚胺离子活化。在2,4-己二醛甲醇的2:1偶联中也证明了纯胺促进了形式逆电子需求的Diels-Alder环加成反应。这些反应证明了双重属/胺催化的概念,并且胺促进了形式逆电子需求Diels–Alder环加成反应。它们与已知的有机催化Diels-Alder反应的例子不同,在Diels-Alder反应中,二亲和物的亚胺离子活化或二胺活化。
  • Bi-functional complexes and methods for making and using such complexes
    申请人:Gouliaev Alex Haahr
    公开号:US11225655B2
    公开(公告)日:2022-01-18
    The present invention is directed to a method for the synthesis of a bi-functional complex comprising a molecule part and an identifier oligonucleotide part identifying the molecule part. A part of the synthesis method according to the present invention is preferably conducted in one or more organic solvents when a nascent bi-functional complex comprising an optionally protected tag or oligonucleotide identifier is linked to a solid support, and another part of the synthesis method is preferably conducted under conditions suitable for enzymatic addition of an oligonucleotide tag to a nascent bi-functional complex in solution.
    本发明涉及一种合成双功能复合物的方法,该复合物包括分子部分和识别分子部分的识别寡核苷酸部分。根据本发明的合成方法的一部分优选在一种或多种有机溶剂中进行,此时包含可选保护标签或寡核苷酸标识符的新生双功能复合物与固体支持物相连接,合成方法的另一部分优选在适合于将寡核苷酸标签酶加到溶液中的新生双功能复合物的条件下进行。
  • BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES
    申请人:Nuevolution A/S
    公开号:EP2558577A1
    公开(公告)日:2013-02-20
  • BI-FUNCTINAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES
    申请人:Gouliaev Alex Haahr
    公开号:US20130281324A1
    公开(公告)日:2013-10-24
    The present invention is directed to a method for the synthesis of a bi-functional complex comprising a molecule part and an identifier oligonucleotide part identifying the molecule part. A part of the synthesis method according to the present invention is preferably conducted in one or more organic solvents when a nascent bi-functional complex comprising an optionally protected tag or oligonucleotide identifier is linked to a solid support, and another part of the synthesis method is preferably conducted under conditions suitable for enzymatic addition of an oligonucleotide tag to a nascent bi-functional complex in solution.
  • [EN] BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES<br/>[FR] COMPLEXES BIFONCTIONNELS ET PROCÉDÉS DE FABRICATION ET D'UTILISATION DE TELS COMPLEXES
    申请人:NUEVOLUTION AS
    公开号:WO2011127933A1
    公开(公告)日:2011-10-20
    The present invention is directed to a method for the synthesis of a bi-functional complex comprising a molecule part and an identifier oligonucleotide part identifying the molecule part. A part of the synthesis method according to the present invention is preferably conducted in one or more organic solvents when a nascent bi-functional complex comprising an optionally protected tag or oligonucleotide identifier is linked to a solid support, and another part of the synthesis method is preferably conducted under conditions suitable for enzymatic addition of an oligonucleotide tag to a nascent bi-functional complex in solution.
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