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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.
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页码:545 / 555
页数:11
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