Publication | Closed Access
6‐Trifluoromethyl‐Phenanthridines through Radical Trifluoromethylation of Isonitriles
350
Citations
40
References
2013
Year
HalogenationDerivative (Chemistry)Radical ApproachRadical PrecursorsOrganic ChemistryRadical TrifluoromethylationTransition MetalChemistryHeterocycle ChemistryPharmacologyChemical Derivative
A radical approach toward 6-perfluoroalkylphenanthridines employs the Togni reagent or derivatives thereof as radical precursors and occurs in the absence of a transition metal. Bu4NI is applied as radical initiator and phenanthridines are formed in good to excellent yields. In contrast to the currently intensively investigated trifluoromethylation of arenes, the arene core is formed during the trifluoromethylation in this approach. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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