1991
DOI: 10.1039/c39910000473
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Ruthenium-catalysed aerobic oxidation of alcohols via multistep electron transfer

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Cited by 191 publications
(66 citation statements)
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“…[21,22] Three different olefins were studied, cyclohexene, allylbenzene and 1-octene. The corresponding allylic acetates were formed in moderate yields (Table 2).…”
Section: Catalytic Activitymentioning
confidence: 99%
“…[21,22] Three different olefins were studied, cyclohexene, allylbenzene and 1-octene. The corresponding allylic acetates were formed in moderate yields (Table 2).…”
Section: Catalytic Activitymentioning
confidence: 99%
“…All NMR spectra were recorded in CDCl 3 or [D 6 ]DMSO solutions with tetramethylsilane as the internal standard for 1 H NMR and CDCl 3 for 13 C NMR. Analytical gas chromatography was performed with a Varian 3400 GC with FID detector connected to a Varian 4270 computing integrator.…”
Section: Methodsmentioning
confidence: 99%
“…Among the various transition-metal catalysts, much attention has been focused on the ability of ruthenium catalysts, since they have often been used for hydrogenation and transfer hydrogenation reactions [5] as well as dehydrogenation and oxidation reactions [6,7]. In fact, some success has been realized using ruthenium catalysts in alcohol oxidation with NaIO 4 [8], tert-butyl hydroperoxide [9,10], chloramine-T [11], amine-N-oxide [11], iodosylbenzene [12], NaBrO 3 [13,14], benzoquinone/Co(salen) [15][16][17], H 2 O 2 [18], and TEMPO [19] as oxidants. However, there are few examples of a ruthenium-catalyzed real aerobic oxidation of alcohols without hydrogen acceptors [20,21].…”
Section: Introductionmentioning
confidence: 99%