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- W2117433650 abstract "N -Methylated amides ( N ,4-dimethylbenzamide and N -methylcyclohexanecarboxamide) were systematically subjected to chemical transformations, namely, N -tosylation followed by nucleophilic substitution. The amide function was converted to the corresponding carboxylic acid, esters, amides, aldehyde, and ketone upon treatment with hydroxide, alkoxide, amine, diisobutylaluminium hydride and Grignard reagent, respectively. In these transformations, N -methyl- N -tosylcarboxamides behave like a Weinreb amide. Similarly, N -methyl-5-phenylisoxazole-3-carboxamide was converted into 3-functionalized isoxazole derivatives. Since the amide was prepared by the cycloaddition reaction of ethynylbenzene and N -methylcarbamoylnitrile oxide, the nitrile oxide served as the equivalent of the nitrile oxides bearing a variety of functional groups such as carboxy, alkoxycarbonyl, carbamoyl, acyl and formyl moieties." @default.
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- W2117433650 date "2015-07-23" @default.
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- W2117433650 title "Development of variously functionalized nitrile oxides" @default.
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- W2117433650 doi "https://doi.org/10.3762/bjoc.11.138" @default.
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