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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >REACTIONS OF ALKYLATION OF BIOLOGICALLY INTERESTING TRIAZOLO[4,5-g]QUINOLINES AND TRIAZOLO[4,5-g]QUINOLINE-1- OXIDES WITH ELECTROPHILIC REAGENTS
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REACTIONS OF ALKYLATION OF BIOLOGICALLY INTERESTING TRIAZOLO[4,5-g]QUINOLINES AND TRIAZOLO[4,5-g]QUINOLINE-1- OXIDES WITH ELECTROPHILIC REAGENTS

机译:亲电试剂对生物有趣的三唑并[4,5-g]喹啉和三唑并[4,5-g]喹诺啉-1-氧化物的烷基化反应

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摘要

With the aim to improve the biological activities discovered for compounds containing the triazolo[4,5-g]quinoline nucleus, we describe the chemical behaviour of 4-chlorotriazolo[4,5-g]quinolines (1a,b) and some its triazolo-N1-oxide derivatives (1c-e and II) with electrophilic reagents in order to optimize the synthetic pathways for obtaining both mixtures of N_(1,2,3)-alkyl isomers and selectively N1-O-alkyl derivatives.
机译:为了改善发现的含有三唑并[4,5-g]喹啉核的化合物的生物活性,我们描述了4-氯三唑并[4,5-g]喹啉(1a,b)及其一些三唑的化学行为。 -N1-氧化物衍生物(1c-e和II)与亲电试剂,以优化合成途径,以同时获得N_(1,2,3)-烷基异构体和选择性N1-O-烷基衍生物的混合物。

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