Facile Synthesis of [1,2,3]-Triazole-Fused Isoindolines, Tetrahydroisoquinolines, Benzoazepines and Benzoazocines by Palladium-Copper Catalysed Heterocyclisation

被引:27
作者
Brahma, Kaushik [1 ]
Achari, Basudeb [1 ]
Chowdhury, Chinmay [1 ]
机构
[1] Indian Inst Chem Biol, Div Chem, CSIR, 4 Raja SC Mullick Rd, Kolkata 700032, India
来源
SYNTHESIS-STUTTGART | 2013年 / 45卷 / 04期
关键词
1,2,3-triazoles; nitrogen heterocycles; intramolecular reactions; azide-alkyne cycloaddition; bis-heteroannulations; CLICK CHEMISTRY; 1,3-DIPOLAR CYCLOADDITIONS; BIOLOGICAL-ACTIVITY; DIRECT ARYLATIONS; INHIBITORS; ANTAGONISTS; RECEPTOR; TRIAZOLE; ANALOGS; ALKYNES;
D O I
10.1055/s-0032-1316839
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An elegant method for the synthesis of 1,2,3-triazoles fused with five-, six-, seven- and eight-membered benzoheterocycles, including isoindoline, tetrahydroisoquinoline, benzoazepine and benzoazocine, has been developed via palladium-copper catalysed reactions in one-pot. The broad scope of this reaction was illustrated by effecting bis-heteroannulations, synthesis of uracil derivatives of biological interest, and employment of acetylene gas as an inexpensive substrate. The reactions are experimentally simple and utilise easily accessible substrates of different types.
引用
收藏
页码:545 / 555
页数:11
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