{"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}
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.
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.