首页> 外文期刊>Molecular diversity >Ethyl 3-(2,4-dioxocyclohexyl)propanoate as a novel precursor for N-substituted 4,4a,5,6-tetrahydroquinoline-2,7(1H,3H)-diones and their corresponding 3,4-dihydro-7-hydroxyquinolin-2(1H)-ones and 7-hydroxyquinolin-2(1H)-ones synthesis
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Ethyl 3-(2,4-dioxocyclohexyl)propanoate as a novel precursor for N-substituted 4,4a,5,6-tetrahydroquinoline-2,7(1H,3H)-diones and their corresponding 3,4-dihydro-7-hydroxyquinolin-2(1H)-ones and 7-hydroxyquinolin-2(1H)-ones synthesis

机译:3-(2,4-二氧环己基)丙酸乙酯作为N-取代的4,4a,5,6-四氢喹啉-2,7(1H,3H)-二酮及其相应的3,4-二氢-7-的新型前体羟基喹啉-2(1H)-one和7-羟基喹啉-2(1H)-one的合成

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摘要

Ethyl 3-(2,4-dioxocyclohexyl)propanoate has been explored as a precursor for the synthesis of N-substituted 4,4a,5,6-tetrahydroquinoline-2,7(1H,3H)-diones following conventional protecvtion, selective amidation, and deprotective-cyclization approaches. Moreover, a facile process for the selective dehydrogenative aromatization of these diones was developed to afford the corresponding N-substituted 3,4-dihydro-7-hydroxyquinolin-2(1H)-ones and N-substituted 7-hydroxyquinolin-2(1H)-ones under mild conditions.
机译:已经研究了3-(2,4-二氧代环己基)丙酸乙酯作为常规保护,选择性酰胺化后合成N-取代的4,4a,5,6-四氢喹啉-2,7(1H,3H)-二酮的前体,以及脱保护环化方法。此外,开发了用于这些二酮的选择性脱氢芳构化的简便方法,以提供相应的N-取代的3,4-二氢-7-羟基喹啉-2(1H)-酮和N-取代的7-羟基喹啉-2(1H) -在温和的条件下。

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