Issue 12, 2024

Decarboxylative 1,3-dipolar cycloadditions of l-proline

Abstract

1,3-Dipolar cycloaddition is one of the important chemical reactions between a 1,3-dipole and a dipolarophile to construct a five-membered heterocyclic compound. As an available α-amino acid reactant, L-proline is extensively used in 1,3-dipolar cycloaddition reactions. A diverse spectrum of bioactive spiro and fused N-heterocycles is obtained through this synthetic approach. In this review, we have described the use of L-proline in the synthesis of various spiro- and fused heterocyclic scaffolds.

Graphical abstract: Decarboxylative 1,3-dipolar cycloadditions of l-proline

Article information

Article type
Review Article
Submitted
29 Nov 2023
Accepted
02 Feb 2024
First published
13 Mar 2024
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2024,14, 8481-8501

Decarboxylative 1,3-dipolar cycloadditions of L-proline

F. Doraghi, A. Serajian, S. Karimian, M. Ghanbarlou, F. Moradkhani, B. Larijani and M. Mahdavi, RSC Adv., 2024, 14, 8481 DOI: 10.1039/D3RA08160E

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