吲哚啉- 3 -酮的合成方法

IF 2.8 4区 化学 Q1 CHEMISTRY, ORGANIC
Deeksha , Dashrath Choudhary , Indra Kumar Gurjar , Abhishek P. Menon , Dr. Archana R. Deokar , Dr. Ritesh Singh
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引用次数: 0

摘要

吲哚啉- 3 - 1是天然存在的生物活性生物碱、染料和合成化合物的重要核心。尽管该核心具有有趣的生物学特征,但相对于其充分探索的异构体吲哚啉- 2 - 1,该核心受到的关注较少。在此,我们回顾了过去十年(2014 - 2024)构建该氧化吲哚基序的合成策略。涵盖了金属介导和无金属的方法,并讨论了关键反应和策略中普遍存在的机制场景。这个一站式的平台无疑将丰富研究人员,并有助于扩大这一领域的研究领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthetic Approaches to Access Indolin‐3‐ones
Indolin‐3‐one constitutes an important core in naturally occurring bio‐active alkaloids, dyes, and synthetic compounds. Though endowed with an interesting biological profile, this core received comparatively less attention than its well‐explored isomer indolin‐2‐one. Herein, we review the synthetic strategies for constructing this oxygenated indole motif during the past decade (2014‐2024). The metal‐mediated and metal‐free methods have been covered, with a discussion of the key reactions and the mechanistic scenario prevailing in the strategies. This one‐stop platform will undoubtedly enrich the researchers and help expand the research domain in this area.
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来源期刊
CiteScore
4.70
自引率
3.70%
发文量
372
期刊介绍: Organic chemistry is the fundamental science that stands at the heart of chemistry, biology, and materials science. Research in these areas is vigorous and truly international, with three major regions making almost equal contributions: America, Europe and Asia. Asia now has its own top international organic chemistry journal—the Asian Journal of Organic Chemistry (AsianJOC) The AsianJOC is designed to be a top-ranked international research journal and publishes primary research as well as critical secondary information from authors across the world. The journal covers organic chemistry in its entirety. Authors and readers come from academia, the chemical industry, and government laboratories.
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