Generation methods aldoxime oxidation

Oxidation of aldoximes 327 with sodium hypochlorite or NBS is one of the best-known methods for generation of nitrile oxides (Equation 73) <1999BCJ2277>. 

Cycloaddition reactions of nitrile oxides continue to be the source of new isoxazoles and dihydroisoxazoles. The oxidation of a-hydroxyimino acids 1 by ammonium hexanitratocerium(IV) has provided a new method of generation of benzonitrile oxide and other nitrile oxides on the other hand the oxime 2 is simply dehydrogenated by this oxidant to produce benzoylnitrile oxide <99BSJ2277>. Manganese dioxide has also been used to oxidise aldoximes to nitrile oxides the reaction is most efficient with methyl (hydroxyimino)acetate <99TL5605>. ... 

Chlorination of aldoximes. NCS converts aryl aldoximes to hydroxamic acid chlorides without significant chlorination of the aryl group. This reaction has been used for a novel synthesis of nitrile oxides. Thus reaction of salicylaldoxime (1) with NCS followed by dehydrochlorination with pyridine generates a nitrile oxide, which is trapped by styrene to give the isoxazoline 2. The N-O bond can be cleaved by catalytic hydrogenation to 3, which is converted into the chalcone 4 on elimination of water. This product can be converted by classical methods to the flavanone 5 and the flavone 6. An analogous route can be used to synthesize 2-... 

Di-(2,3,4,6-tetra-0-acetyl-a-D-mannopyranosyl)-l,2,5-oxadiazole 2-oxide 306 was synthesized from D-mannose 305 by a route involving dimerization of mannopyranosyl nitrile oxide as the key step. Three methods were used for the generation of the nitrile oxide isocyanate-mediated dehydration of nitromethylmannose derivatives, treatment of aldoxime with aqueous hypochlorite, and base-induced dehydrochlorination of hydroximoyl chloride (Scheme 76) <2001TL4065, 2002T8505>. 

Some recent advances have been reported in oxime oxidation, including the in situ generation of peroxytrifluoroacetic acid from the reaction of urea hydrogen peroxide complex with TFAA in acetonitrile at 0 °C This method gives good yields of nitroalkanes from aldoximes but fails with ketoximes. 

Apart from a few stable species, nitrile oxides exhibit a high tendency toward dimerization to furoxans for this reason, several methods have been developed for the in situ generation of such dipoles in the presence of the desired acceptor. The most common procedures involve thermal or base-mediated deydrohalogenation of hydroxymoyl halides, oxidation of aldoximes, and dehydration of primary nitroalkanes <1984CHEC(6)1>. 

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