首页> 外文期刊>Chemistry Select >Phenanthroline-t BuONa Promoted Intramolecular C-H Arylation of 1,5-Diaryl-1,2,3-Triazoles for Efficient Synthesis of Triazolophenanthridines
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Phenanthroline-t BuONa Promoted Intramolecular C-H Arylation of 1,5-Diaryl-1,2,3-Triazoles for Efficient Synthesis of Triazolophenanthridines

机译:苯鞭毛氨酸-T buona促进了1,5-二芳基1,2,3-三唑的分子内C-H芳基化,用于有效合成三氯苯甲烷

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摘要

The first example of phenanthroline- t BuONa promoted intra- molecular C-H arylation of 1,5-diaryl-1,2,3-triazoles without the involvement of transition metals has been developed. Various fused 1,5-disubstituted-1,2,3-triazoles of triazolophe- nanthridines were prepared with excellent yields and high site- selectivity via simple and efficient intramolecular cyclization by using the 1,10-phenanthroline- t BuONa reaction system.
机译:已经开发了未经过渡金属参与的1,5-二芳基-1,2,3-三唑的菲纳酚thuona的第一个例子。 通过使用1,10-10-苯磺胺 - 胰蛋白酶胰蛋白酶的反应系统,通过简单有效的分子内环化来制备各种三唑酚纳米氨酸的1,5-二取代1,2,3-三唑的三唑酚 - 纳米氨酸。

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