吲哚-2-羧基酰胺:用于合成不同取代的多环吲哚结构的多功能合成手柄。

IF 2.9 3区 化学 Q1 CHEMISTRY, ORGANIC
Akshay Kamble, Priyanka Deore, Vanshika Agrawal, Adesh Chauhan, Haneesha Gulipelli, Satyasheel Sharma
{"title":"吲哚-2-羧基酰胺:用于合成不同取代的多环吲哚结构的多功能合成手柄。","authors":"Akshay Kamble, Priyanka Deore, Vanshika Agrawal, Adesh Chauhan, Haneesha Gulipelli, Satyasheel Sharma","doi":"10.1039/d5ob00761e","DOIUrl":null,"url":null,"abstract":"<p><p>Indoles are among the most important N-heterocycles found in natural products, with a wide range of biological and pharmacological properties. The synthesis of naturally occurring complex indole derivatives as well as bioactive synthetic molecules has progressed tremendously. Since many of the bioactive, naturally occurring indole molecules possess polycyclic frameworks, it became essential to develop these scaffolds. In this context, indole derivatives have been utilized as precursors for the synthesis of many important polycyclic indole frameworks. These polycyclic indole molecules also include a fused indole motif. In this regard, there are many fused indole ring systems which can be accessed by indole-2-carboxamide as a key precursor through intramolecular and intermolecular cyclization reactions. This review summarizes the synthetic advancements for the construction of polycyclic fused indole molecules, which have indole-2-carboxamide as a synthetic precursor, and also discusses the synthetic potential and perspective of this essential scaffold. Furthermore, the reaction mechanism of the formation of various fused polycyclic indoles has also been discussed.</p>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":" ","pages":""},"PeriodicalIF":2.9000,"publicationDate":"2025-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Indole-2-carboxamide: a versatile synthetic handle for the synthesis of diversely substituted polycyclic indole structures.\",\"authors\":\"Akshay Kamble, Priyanka Deore, Vanshika Agrawal, Adesh Chauhan, Haneesha Gulipelli, Satyasheel Sharma\",\"doi\":\"10.1039/d5ob00761e\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Indoles are among the most important N-heterocycles found in natural products, with a wide range of biological and pharmacological properties. The synthesis of naturally occurring complex indole derivatives as well as bioactive synthetic molecules has progressed tremendously. Since many of the bioactive, naturally occurring indole molecules possess polycyclic frameworks, it became essential to develop these scaffolds. In this context, indole derivatives have been utilized as precursors for the synthesis of many important polycyclic indole frameworks. These polycyclic indole molecules also include a fused indole motif. In this regard, there are many fused indole ring systems which can be accessed by indole-2-carboxamide as a key precursor through intramolecular and intermolecular cyclization reactions. This review summarizes the synthetic advancements for the construction of polycyclic fused indole molecules, which have indole-2-carboxamide as a synthetic precursor, and also discusses the synthetic potential and perspective of this essential scaffold. Furthermore, the reaction mechanism of the formation of various fused polycyclic indoles has also been discussed.</p>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-06-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5ob00761e\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5ob00761e","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

摘要

吲哚是天然产物中最重要的n -杂环化合物之一,具有广泛的生物学和药理学性质。天然存在的吲哚复合物衍生物的合成以及生物活性合成分子的合成取得了巨大的进展。由于许多具有生物活性的天然吲哚分子具有多环框架,因此开发这些支架变得至关重要。在这种情况下,吲哚衍生物已被用作合成许多重要的多环吲哚框架的前体。这些多环吲哚分子还包括一个融合的吲哚基序。在这方面,有许多融合的吲哚环体系可以通过分子内和分子间的环化反应被吲哚-2-羧酰胺作为关键前体进入。本文综述了以吲哚-2-羧基酰胺为前体的多环融合吲哚分子的合成进展,并讨论了这一重要支架的合成潜力和前景。此外,还讨论了各种熔融多环吲哚的反应机理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Indole-2-carboxamide: a versatile synthetic handle for the synthesis of diversely substituted polycyclic indole structures.

Indoles are among the most important N-heterocycles found in natural products, with a wide range of biological and pharmacological properties. The synthesis of naturally occurring complex indole derivatives as well as bioactive synthetic molecules has progressed tremendously. Since many of the bioactive, naturally occurring indole molecules possess polycyclic frameworks, it became essential to develop these scaffolds. In this context, indole derivatives have been utilized as precursors for the synthesis of many important polycyclic indole frameworks. These polycyclic indole molecules also include a fused indole motif. In this regard, there are many fused indole ring systems which can be accessed by indole-2-carboxamide as a key precursor through intramolecular and intermolecular cyclization reactions. This review summarizes the synthetic advancements for the construction of polycyclic fused indole molecules, which have indole-2-carboxamide as a synthetic precursor, and also discusses the synthetic potential and perspective of this essential scaffold. Furthermore, the reaction mechanism of the formation of various fused polycyclic indoles has also been discussed.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry 化学-有机化学
CiteScore
5.50
自引率
9.40%
发文量
1056
审稿时长
1.3 months
期刊介绍: Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信