研究O-tosyl alkyl amidoximes與3-dimethylaminopropenone derivatives於適當金屬鹽條件下進行[3+2]環加成反應。O-tosyl alkyl amidoximes 可以由alkyl nitriles與hydroxylamine進行親核加成反應得到alkyl amidoximes，而alkyl amidoximes接著與TsCl進行O-tosylation得到。同時，3-dimethylaminopropenones可以由methyl ketones與N,N-dimethylforamide-dimethylacetal (DMF-DMA)進行反應得到。不幸地，O-tosyl aryl amidoximes不能以相同步驟被製備。找尋另一替代方式，發現oxadiazolones可以進行[3+2]環加成反應，而其可以由aryl oximes與carbonylimidazole (CDI)進行兩次親核加成與消去反應所製備。我們的研究顯示出以O-tosyl alkyl amidoximes及aryl oxadiazolones作為反應物，與3-dimethylaminopropenones進行[3+2]環加成反應，可以作為一新穎的方式得到4-acyl-2-substituted imidazoles。

A systematic screening of metal ion catalysts for the [3+2] cycloaddition of O-tosyl alkyl amidoximes with 3-dimethylaminopropenone derivatives was studied. O-Tosyl alkyl amidoximes can be obtained by nucleophilic addition of hydroxylamine to alkyl nitriles followed by tosylation with TsCl. Meanwhile, 3-dimethylaminopropenones were obtained from the reaction of methyl ketones with N,N-dimethylformamide-dimethylacetal. Unfortunately, O-tosyl aryl amidoximes cannot be obtained by the same process. Alternatively, aryl oxadiazolones were obtained by nucleophilic addition and elimination of aryl oximes to carbonyldiimidazole. Our investigation showed that iron(III)-catalyzed [3+2] cycloaddition of O-tosyl alkyl amidoximes and aryl oxadiazolones with 3-dimethylaminopropenones can serve as a novel approach toward 4-acyl-2-substituted imidazoles.

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