Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
69190 | Journal of Molecular Catalysis A: Chemical | 2006 | 4 Pages |
Metallophthalocyanines bearing substituents are found to be efficient catalysts for nitrene transfer reactions. Under optimized reaction conditions, aziridination of alkenes and amidation of CH bonds with PhI = NTs by using 3-trifluromethylphenyoxy-substituted phthalocyanine-iron complex led to the highest yields of 90% and 85% for 4-methylstyrene and 4-ethyltoluene, respectively.
Graphical abstractMetallophthalocyanines bearing substituents are found to be efficient catalysts for nitrene transfer reaction. Under optimized reaction conditions, aziridination of alkenes and amidation of CH bonds with PhI = NTs by using 3-trifluromethylphenyoxy-substituted iron-phthalocyanine complex led to the highest yields of 90% and 85% for 4-methylstyrene and 4-methylethylbenzene, respectively. Figure optionsDownload full-size imageDownload as PowerPoint slide