Epoxidation of Alkenes Catalyzed by Iron(III) Schiff Base Chelates. A Monooxygenase Model
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چکیده
منابع مشابه
Toluene monooxygenase-catalyzed epoxidation of alkenes.
Several toluene monooxygenase-producing organisms were tested for their ability to oxidize linear alkenes and chloroalkenes three to eight carbons long. Each of the wild-type organisms degraded all of the alkenes that were tested. Epoxides were produced during the oxidation of butene, butadiene, and pentene but not hexene or octadiene. A strain of Escherichia coli expressing the cloned toluene-...
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Oxovanadium(IV), manganese(II) and copper(II) complexes of a Schiff base ligand derived from 2,4-dihydroxyacetophenone and 1,2-diaminocyclohexane have been encapsulated in the nanocavity of zeolite-Y by flexible ligand method and characterized by metal analysis, IR spectroscopic studies and X-ray diffraction patterns. The encapsulated complexes abbreviated here as CuL-Y, MnL-Y and VOL-Y catalyz...
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Iron (III) meso-tetrakis(p-sulfonatophenyl)-β-octabromoporphyrin supported on Amberlite IRA- 400 [Fe(Br8 TPPS)-Ad-400] is a robust and efficient catalyst for oxidation of alkenes and alcohols at room temperature. The catalyst exhibits a high activity and stability in hydrocarbon oxidation by H2 O2 . The method was useful in the oxidation of various primary, secondary-aliphatic, alicyclic and ar...
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Ag and Ru nanoparticles stabilized by H5PV2Mo10O40, prepared by a sequence of redox reactions and supported on alpha-alumina, were effective catalysts for the direct aerobic epoxidation of alkenes in the liquid phase.
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ژورنال
عنوان ژورنال: Bulletin of the Chemical Society of Japan
سال: 1989
ISSN: 0009-2673,1348-0634
DOI: 10.1246/bcsj.62.1325