首页> 外文期刊>Beilstein journal of organic chemistry. >Cascade alkylarylation of substituted N-allylbenzamides for the construction of dihydroisoquinolin-1(2H)-ones and isoquinoline-1,3(2H,4H)-diones
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Cascade alkylarylation of substituted N-allylbenzamides for the construction of dihydroisoquinolin-1(2H)-ones and isoquinoline-1,3(2H,4H)-diones

机译:N-烯丙基苯甲酰胺的级联烷基芳基化反应,用于构建二氢异喹啉-1(2H)-酮和异喹啉-1,3(2H,4H)-二酮

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An oxidative reaction for the synthesis of 4-alkyl-substituted dihydroisoquinolin-1(2 H )-ones with N -allylbenzamide derivatives as starting materials has been developed. The radical alkylarylation reaction proceeds through a sequence of alkylation and intramolecular cyclization. The substituent on the C–C double bond was found to play a key role for the progress of the reaction to give the expected products with good chemical yields. Additionally, N -methacryloylbenzamides were also suitable substrates for the current reaction and provided the alkyl-substituted isoquinoline-1,3(2 H ,4 H )-diones in good yield.
机译:已开发出以N-烯丙基苯甲酰胺衍生物为起始原料合成4-烷基取代的二氢异喹啉-1(2 H)-ones的氧化反应。自由基烷基芳基化反应通过一系列烷基化和分子内环化反应进行。人们发现,CC双键上的取代基在反应进程中起关键作用,以提供具有良好化学收率的预期产物。另外,N-甲基丙烯腈苯甲酰胺也是当前反应的合适底物,并以良好的产率提供了烷基取代的异喹啉-1,3(2H,4H)-二酮。

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