منابع مشابه
Iron-catalyzed epoxidation of olefins using hydrogen peroxide†
90 A practical method of olefin epoxidation was developed by combining FeCl3·6H2O and 1methylimidazole in acetone using H2O2 as the terminal oxidant. This system showed very good reactivity toward epoxidation of both terminal and substituted alkenes. The use of tridentate and tetradentate amine-bis(phenolate) ligands as additives was also examined. Modest improvement in selectivity was achieved...
متن کاملCatalytic Epoxidation of Olefins by Nanolayered Polyoxomolybdate [4,4´-H2bipy][Mo7O22].(H2O)
A two-dimensional nanolayered polyoxomolybdate, [4,4´-H2bipy] [Mo7O22].H2O (1), where 4,4´-bipy = 4,4´-bipyridine, was prepared and characterized by FT-IR and atomic absorption spectroscopies, transmission electron microscopy (TEM), X-ray single crystal and powder diffraction (XRD), and thermogravimetric analysis. The catalytic performance of 1 was assessed in the epoxidation of some olefins em...
متن کاملDesign and Synthesis of Binaphthol-Derived Chiral Ketone Catalysts for Dioxirane-Mediated Asymmetric Epoxidation of Olefins
Binaphthol-derived chiral ketones 1a-c were synthesized and were shown to serve as active catalysts for asymmetric epoxidation of olefins using Oxone®, although their enantioselectivities were not high. However, very interestingly, the stereochemical outcome of the resulting epoxides implicates that in the epoxidation using 1ac, the planar transition state may be more favorable than the spiro t...
متن کاملNovel one-pot process for the synthesis of 1,3-thiazoles via organocatalysed epoxidation of nitro-olefins.
A facile one-pot two-step process for the synthesis of 1,3-thiazole heterocycles via organocatalytic epoxidation of nitro-olefins with the t-BuOOH/DBU system, and subsequent reaction of α-nitro-epoxides with thioamides under mild conditions has been developed.
متن کاملActivation of hydrogen peroxide by ionic liquids: mechanistic studies and application in the epoxidation of olefins.
Imidazolium-based ionic liquids that contain perrhenate anions are very efficient reaction media for the epoxidation of olefins with H2O2 as an oxidant, thus affording cyclooctene in almost quantitative yields. The mechanism of this reaction does not follow the usual pathway through peroxo complexes, as is the case with long-known molecular transition-metal catalysts. By using in situ Raman, FT...
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ژورنال
عنوان ژورنال: Journal of Synthetic Organic Chemistry, Japan
سال: 1968
ISSN: 0037-9980,1883-6526
DOI: 10.5059/yukigoseikyokaishi.26.506