Iodine-catalyzed oxidative annulation of 3-cyanoacetylindoles with benzylamines: facile access to 5-(3-indolyl)oxazoles

Iodine-catalyzed oxidative annulation of 3-cyanoacetylindoles with benzylamines: facile access to 5-(3-indolyl)oxazoles
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碘催化 3-氰基乙酰吲哚与苄胺的氧化环化:轻松获得 5-(3-吲哚基)恶唑

DOI:
10.1039/c8ob00833g
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发表时间:
2018-05-21
影响因子:
3.2
通讯作者:
Liu, Peijun
Liu, Peijun
中科院分区:
化学3区
文献类型:
--
作者:
Liu, Xiaozu;Zhou, Yuxiang;Liu, Peijun

文献摘要

被引文献

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已经开发出一种碘催化的 3-氰基乙酰吲哚与苄胺的氧化成环反应。该反应能够在温和的条件下方便地合成各种具有广泛官能团兼容性的5-(3-吲哚基)恶唑。
An iodine-catalyzed oxidative annulation of 3-cyanoacetylindoles with benzylamines has been developed. This reaction enables the convenient synthesis of a variety of 5-(3-indolyl)oxazoles under mild conditions with broad functional group compatibility.