炔丙基
化学
碳阳离子
亲核细胞
分子内力
炔烃
有机化学
环加成
三键
有机合成
胺气处理
电泳剂
亲核加成
组合化学
催化作用
双键
作者
Amit Ranjan Pandey,Durgesh Kumar Tiwari,Aditya Prakhar,Devendra Mishra,S. SHARMA
标识
DOI:10.1007/s00706-022-02927-7
摘要
In the area of drug discovery, nitrogen/oxygen-based heterocycles have been utilized as key intermediates and have great attention in organic chemistry. A literature survey reveals that in the past two decades propargyl alcohols and propargyl amines contributed significantly to the synthesis of such bioactive heterocycles. Propargyl alcohols and propargyl amine precursors are alkyne-based compounds and can be easily converted to propargylic carbocations. The nucleophilic nature of the triple bond and electrophilic nature of furnished carbocations from propargyl alcohols and propargyl amines makes these intermediates highly reactive and useful for the synthesis of various heterocycles by cycloaddition, intermolecular/intramolecular-cyclization, cycloisomerization, cyclo-condensation reactions. Here in this review, we are going to summarize important and useful methodologies for the development of nitrogen and oxygen-based heterocycles using propargyl alcohols and propargyl amines.Graphical abstract
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