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首页> 外文期刊>Egyptian Journal of Chemistry >Reaction of 2,6-Bis(4-azidobenzyIidene)-4-methyl-cyclohexanone with Organophosphorus Reagents. Synthesis of Some Benzylidene-1, 2, 3-triazole Derivatives
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Reaction of 2,6-Bis(4-azidobenzyIidene)-4-methyl-cyclohexanone with Organophosphorus Reagents. Synthesis of Some Benzylidene-1, 2, 3-triazole Derivatives

机译:2,6-双(4-叠氮基亚苄基)-4-甲基-环己酮与有机磷试剂的反应。某些亚苄基-1,2,3-三唑衍生物的合成

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摘要

TRIPHENYLPHOSPHINE (1) reacts with 2,6-bis(4-azido-benzylidene)-4-raethylcyclohexanone (4) to give the respective triphenylphosphinylidenetriaz-1-enyl (5a) and triphenylphosphinylidene-amino (5b). Moreover, reaction of aryl azide (4) with trisdimethy-laminophosphine (2) in refluxing toluene afforded the new products (6a, b). On the other hand, phosphorus ylides (3a-d) react with azidobenz-ylidene (4) to give the corresponding l,5-disubstituted-l,2,3-triazoles (7a-d) and triphenylphosphine oxide. Possible reaction mechanisms are considered and the structural assignments are based on compatible analytical and spectroscopic results.
机译:三苯膦(1)与2,6-双(4-叠氮基-亚苄基)-4-芳乙基环己酮(4)反应,分别得到三苯基亚膦酰基亚氮基-1-烯基(5a)和三苯基亚膦酰基-氨基(5b)。此外,芳基叠氮化物(4)与三二甲基-氨基膦(2)在回流的甲苯中反应,得到新产物(6a,b)。另一方面,磷酰基化物(3a-d)与叠氮基亚苄基(4)反应,得到相应的1,5-二取代-1,2,3-三唑(7a-d)和三苯基氧化膦。考虑了可能的反应机理,并且结构分配基于兼容的分析和光谱结果。

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