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Indole as a Versatile Building Block in Cycloaddition Reactions: Synthesis of Diverse Heterocyclic Frameworks.
Baruah, Biswajita; Pegu, Choitanya Dev; Deb, Mohit L.
Affiliation
  • Baruah B; Department of Chemistry, Pandu College, Guwahati, Assam, 781012, India. biswajitabaruah@gmail.com.
  • Pegu CD; Department of Chemistry, Madhabdev University, Lakhimpur, Assam, 784164, India.
  • Deb ML; Advanced Research Centre and Department of Chemistry, University of Science and Technology Meghalaya, Ri-Bhoi, Meghalaya, 793101, India. mohitdd.deb@gmail.com.
Top Curr Chem (Cham) ; 382(2): 18, 2024 May 17.
Article in En | MEDLINE | ID: mdl-38758483
ABSTRACT
Indole, a ubiquitous and structurally versatile aromatic compound, has emerged as a key player in the synthesis of diverse heterocyclic frameworks via cycloaddition reactions. These reactions are completely atom-economical and, hence, are considered as green reactions. This review article provides a comprehensive overview of the pivotal role played by indole in the construction of complex and biologically relevant heterocyclic compounds. Here we explore the chemistry of indole-based cycloadditions, highlighting their synthetic utility in accessing a wide array of heterocyclic architectures, including cyclohepta[b]indoles, tetrahydrocarbazoles, tetrahydroindolo[3,2-c]quinoline, and indolines, among others. Additionally, we discuss the mechanistic insights that underpin these transformations, emphasizing the strategic importance of indole as a building block. The content of this article will certainly encourage the readers to explore more work in this area.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cycloaddition Reaction / Heterocyclic Compounds / Indoles Language: En Journal: Top Curr Chem (Cham) Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cycloaddition Reaction / Heterocyclic Compounds / Indoles Language: En Journal: Top Curr Chem (Cham) Year: 2024 Document type: Article