2009
DOI: 10.1039/b919346b
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A metal-free catalytic system for the oxidation of benzylic methylenes and primary amines under solvent-free conditions

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Cited by 118 publications
(49 citation statements)
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“…Due to the activation, the formation of the corresponding ketones and aldehydes becomes feasible under mild conditions. Oxidations of this kind using Oxone ® [1011], NaOCl [12] or especially peroxides [1319] as the terminal oxidant are quite numerous. However, transformations using molecular oxygen are rare.…”
Section: Introductionmentioning
confidence: 99%
“…Due to the activation, the formation of the corresponding ketones and aldehydes becomes feasible under mild conditions. Oxidations of this kind using Oxone ® [1011], NaOCl [12] or especially peroxides [1319] as the terminal oxidant are quite numerous. However, transformations using molecular oxygen are rare.…”
Section: Introductionmentioning
confidence: 99%
“…5 On this basis, Savelli reported that primary amines can be converted into nitriles using nickel peroxide as a catalyst, generated in situ from nickel and potassium persulfate as a co-oxidant, in a biphasic water-dichloromethane reaction. 6 It has been reported that TBA 4 [a-H 4 SiW 11 O 39 ] can act as a heterogeneous catalyst for the dehydration of primary amides to form the corresponding nitriles. 7 Yanada described a new C-C triple bond cleavage reaction with NIS and TMSN 3 to achieve the corresponding nitriles.…”
mentioning
confidence: 99%
“…The 20 initial weight loss of 5.6 % accompanied by an endothermic reaction below 150 o C is assigned to the loss of adsorbed water and the evaporation of intercalated water molecules. The subsequent weight loss of 21.6 % at 150-300 o C and a broad exothermic peak at 280 o C is due to the loss of water produced by 25 the decomposition and dehydroxylation of Co(OH) 2 hexane, isopropylalcohol, acetone, toluene and acetonitrile are 10 employed as the solvent, respectively (entry 2-6). This suggests that the aprotic solvents with larger dielectric constant are beneficial to the enhancing of the conversion of 4,4'difluorobenzophenone.…”
Section: Resultsmentioning
confidence: 99%
“…[1][2][3] The development of 20 catalysts for benzylic oxidation has therefore attracted considerable interest. In the past decades, tremendous efforts had been devoted to transition-metal catalysts involving Cr, 4,5 Mn, 6,7 Bi, 1 Cu, 8 V, 9,10 Rh, 11 Au 12 , and Fe 13 for benzylic oxidation reactions.…”
Section: Introductionmentioning
confidence: 99%