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首页> 外文期刊>Beilstein journal of organic chemistry. >Efficient synthesis of 5-substituted 2-aryl-6-cyanoindolizines via nucleophilic substitution reactions
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Efficient synthesis of 5-substituted 2-aryl-6-cyanoindolizines via nucleophilic substitution reactions

机译:通过亲核取代反应高效合成5-取代的2-芳基-6-氰基吲哚嗪

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摘要

2-Aryl-6-cyano-7-methyl-5-indolizinones were successfully converted into 2-aryl-5-chloro-6-cyano-7-methylindolizines. The obtained 5-chloroindolizines readily underwent nucleophilic substitution at position 5 leading in high yields to novel 5-functionalised indolizines.Keywords: 5-chloroindolizine, 5-substituted indolizines, 5-indolizinone, nucleophilic substitution
机译:将2-芳基-6-氰基-7-甲基-5-吲哚并酮成功地转化为2-芳基-5-氯-6-氰基-7-甲基吲哚并嗪。所获得的5-氯吲哚并嗪易于在位置5进行亲核取代,从而以高收率生成新颖的5-官能化吲哚嗪。关键词:5-氯吲哚嗪,5-取代吲哚嗪,5-吲哚嗪酮,亲核取代

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