In(OTf)3催化a3环化策略合成吡唑系喹啉衍生物及其发光性能评价

IF 2.5 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Rahul Jamra, Chandi C. Malakar, Sadhika Khullar and Virender Singh
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引用次数: 0

摘要

通过4-甲酰基吡唑-3羧酸酯、取代芳香胺和末端炔的a3偶联,设计了一种In(OTf)3催化合成荧光吡唑系喹啉衍生物的方法。这种策略有几个优点,包括使用现成和廉价的起始材料,广泛的底物范围,可持续的反应条件和高产品收率。该策略适用于克级合成,并且该方法的范围用于合成32种新型吡唑系喹啉衍生物的文库,收率高达96%。对这些吡唑系联喹啉的光物理性质进行了估计,获得了极好的结果,量子产率(ΦF)高达75%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In(OTf)3-catalysed A3-annulation strategy towards the synthesis of pyrazole-tethered quinoline derivatives and assessment of their luminescent properties†

In(OTf)3-catalysed A3-annulation strategy towards the synthesis of pyrazole-tethered quinoline derivatives and assessment of their luminescent properties†

An In(OTf)3-catalysed approach has been devised for the synthesis of fluorescent pyrazole-tethered quinoline derivatives via the A3-coupling of 4-formyl-pyrazole-3-carboxylates, substituted aromatic amines and terminal alkynes. This strategy offers several advantages, including the use of readily available and inexpensive starting materials, broad substrate scope, sustainable reaction conditions and high product yields. This strategy is amenable to gram-scale synthesis, and the scope of this methodology was demonstrated for the synthesis of a library of 32 novel pyrazole-tethered quinoline derivatives, with yields up to 96%. The photophysical properties of these pyrazole-tethered quinolines were estimated and excellent results were obtained with a quantum yield (ΦF) of up to 75%.

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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
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