Synthesis of phenanthridine derivatives via cascade annulation of diaryliodonium salts and nitriles
作者:Jian Li、Hongni Wang、Jiangtao Sun、Yang Yang、Li Liu
DOI:10.1039/c4ob01504e
日期:——
A cascade coupling reaction toward a variety of phenanthridine derivatives has been developed. This cascade transformation proceeds via the copper-catalyzed coupling reaction of diaryliodonium salts and nitriles, and undergoes cyclization into the phenanthridine core.
Transition-metal-free, visible-light induced cyclization of arylsulfonyl chlorides with 2-isocyanobiphenyls to produce phenanthridines
作者:Lijun Gu、Cheng Jin、Jiyan Liu、Hongyan Ding、Baomin Fan
DOI:10.1039/c4cc01487a
日期:——
A visible-light promoted transformation of 2-isocyanobiphenyls and arylsulfonyl chlorides for the synthesis of phenanthridines under oxidant-free and transition-metal-free conditions was described.
2-异氰基联苯和芳基磺酰氯在无氧化剂和过渡金属的条件下,经可见光促进转化合成菲啰啉。
Preparation of Substituted Phenanthridines from the Coupling of Aryldiazonium Salts with Nitriles: A Metal Free Approach
作者:Mani Ramanathan、Shiuh-Tzung Liu
DOI:10.1021/acs.joc.5b00579
日期:2015.5.15
A transition metal free approach for the synthesis of substituted phenanthridines from the coupling reaction of aryldiazonium tetrafluoroborates with nitriles has been developed. This operationally simple protocol proceeds through a substitution of aryldiazonium with nitriles followed by an intramolecular arylation to provide the corresponding phenanthridines in moderate to excellent yields.
Efficient Synthesis of Phenanthridines Using Hendrickson Reagent Initiated Cascade Reaction under Mild Conditions
作者:Lin Chen、Zhu-Jun Yao、Jie Xi、Qing-Li Dong、Guan-Sai Liu、Shaozhong Wang
DOI:10.1055/s-0030-1258081
日期:2010.7
A number of variously substituted phenanthridines have been synthesized using the newly developed methodology under mild conditions. The Hendrickson reagent initiated cascade annulation, which is composed of a mild conversion of stable amide precursor to highly reactive imido-carbonium intermediate and a subsequent intramolecular Friedel-Crafts reaction, successfully served as the key method.
Irradiation of hydrazines with visible-light in the presence of organic dye eosin B generates various types of functional radicals, which are trapped by 2-isocyanobiphenyls to give 6-substituted phenanthridines.