首页> 外文期刊>Tetrahedron >Synthesis of 3-substituted 2-bromoquinolines utilizing 2-bromo-3-lithioquinolines generated by the reaction of 2-(2,2-dibromoethenyl)phenyl isocyanides with butyllithium
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Synthesis of 3-substituted 2-bromoquinolines utilizing 2-bromo-3-lithioquinolines generated by the reaction of 2-(2,2-dibromoethenyl)phenyl isocyanides with butyllithium

机译:利用2-(2,2-二溴乙烯基)苯基异氰酸酯与丁基锂反应生成的2-溴-3-硫代喹啉合成3-取代的2-溴喹啉

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摘要

The first generation of 2-bromo-3-lithioquinolines can be achieved and they are utilized for the preparation of 3-substituted 2-bromoquinolines. Thus, 2-(2,2-dibromoethenyl)phenyl isocyanides are treated with butyllithium in THF at -78 degrees C to generate these novel lithium compounds, which are allowed to react with various electrophiles to afford the corresponding desired products in one-pot. (C) 2015 Elsevier Ltd. All rights reserved.
机译:可以获得第一代2-溴-3-硫代喹啉,并将其用于制备3-取代的2-溴喹啉。因此,将2-(2,2-二溴乙烯基)苯基异氰化物在-78℃下用丁基锂在THF中处理以生成这些新颖的锂化合物,使它们与各种亲电试剂反应以一锅法得到相应的所需产物。 (C)2015 Elsevier Ltd.保留所有权利。

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