Dioxygen epoxidation of cyclic alkenes into their corresponding epoxides was successfully achieved in good yield by using a novel binuclear manganese carboxamide complex as the catalyst and isobutyraldehyde as the cosubstrate.
Metal substituted octachloro-, hexadecachloro- and tetranitrophthalocyanine were synthesized by exposure to microwave irradiation under solvent free and reflux conditions and the products were purified by a new route.
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