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2-[naphthalen-2-yl(phenyl)methyl]benzo[d]oxazole | 1613376-55-8

中文名称
——
中文别名
——
英文名称
2-[naphthalen-2-yl(phenyl)methyl]benzo[d]oxazole
英文别名
2-[Naphthalen-2-yl(phenyl)methyl]-1,3-benzoxazole;2-[naphthalen-2-yl(phenyl)methyl]-1,3-benzoxazole
2-[naphthalen-2-yl(phenyl)methyl]benzo[d]oxazole化学式
CAS
1613376-55-8
化学式
C24H17NO
mdl
——
分子量
335.405
InChiKey
YIKGJYJYWUMSBU-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):
    6.4
  • 重原子数:
    26
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.04
  • 拓扑面积:
    26
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    参考文献:
    名称:
    Synthesis of Triarylmethanes by Palladium-Catalyzed C–H/C–O Coupling of Oxazoles and Diarylmethanol Derivatives
    摘要:
    A PdCl2(MeCN)2/PPhCy2 catalyst couples oxazoles with diarylmethyl carbonates or pivalates to form the corresponding triarylmethanes in good yields. The catalysis involves successive secondary benzylic sp(3) C-O and heteroaromatic sp(2) C-H cleavages and provides an effective access to heteroarene-containing triarylmethanes from nonhalogenated and nonmetalated starting materials, which is complementary to precedented cross-coupling technologies with organic halides and organometallic reagents.
    DOI:
    10.1021/jo5010636
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文献信息

  • Synthesis of Triarylmethanes by Palladium-Catalyzed C–H/C–O Coupling of Oxazoles and Diarylmethanol Derivatives
    作者:Sho Tabuchi、Koji Hirano、Tetsuya Satoh、Masahiro Miura
    DOI:10.1021/jo5010636
    日期:2014.6.20
    A PdCl2(MeCN)2/PPhCy2 catalyst couples oxazoles with diarylmethyl carbonates or pivalates to form the corresponding triarylmethanes in good yields. The catalysis involves successive secondary benzylic sp(3) C-O and heteroaromatic sp(2) C-H cleavages and provides an effective access to heteroarene-containing triarylmethanes from nonhalogenated and nonmetalated starting materials, which is complementary to precedented cross-coupling technologies with organic halides and organometallic reagents.
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