Deployment of Aziridines for the Synthesis of Alkaloids and Their Derivatives
Matthias D’hooghe, Hyun‐Joon Ha, Lingamurthy Macha
Abstract
Matthias D’hooghe, Hyun‐Joon Ha, Lingamurthy Macha
Abstract
Various (activated and non-activated) aziridines with diverse substitution patterns have been deployed successfully as starting materials for the synthesis of a wide variety of alkaloids via suitable functionalization and aziridine ring transformation. Alternatively, the preparation and interception of reactive aziridine intermediates has also been shown to constitute a valid approach toward alkaloid synthesis. This review summarizes aziridine-mediated syntheses of alkaloids, in which the aziridine is mobilized as either a substrate or an advanced synthetic intermediate. 1 Introduction 2 Alkaloids Synthesis from Aziridine Starting Materials 2.1 (2R)- and (2S)-Hydroxymethyl-N-(1-phenylethyl)aziridines 2.2 N-Benzylaziridine-2-carboxylates 2.3 2-Substituted N-Tosyl- or N-Tritylaziridines 2.4 2,3-Disubstituted N-Cbz- or N-Tosylaziridines 2.5 N-DMB-aziridines 3 Alkaloids Synthesis from Aziridines as Key Advanced Synthetic Intermediates 3.1 Alkylative Aziridine Ring Opening 3.2 Arylative Aziridine Ring Opening 3.3 Ring Expansion 3.4 Oxidative Aziridine Ring Opening 3.5 Heteroatomic Nucleophilic Aziridine Ring Opening 3.6 Reductive Aziridine Ring Opening 4 Conclusion
OpenAlex reports 30 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Various (activated and non-activated) aziridines with diverse substitution patterns have been deployed successfully as starting materials for the synthesis of a wide variety of alkaloids via suitable functionalization and aziridine ring transformation. Alternatively, the preparation and interception of reactive aziridine intermediates has also been shown to constitute a valid approach toward alkaloid synthesis. This review summarizes aziridine-mediated syntheses of alkaloids, in which the aziridine is mobilized as either a substrate or an advanced synthetic intermediate. 1 Introduction 2 Alkaloids Synthesis from Aziridine Starting Materials 2.1 (2R)- and (2S)-Hydroxymethyl-N-(1-phenylethyl)aziridines 2.2 N-Benzylaziridine-2-carboxylates 2.3 2-Substituted N-Tosyl- or N-Tritylaziridines 2.4 2,3-Disubstituted N-Cbz- or N-Tosylaziridines 2.5 N-DMB-aziridines 3 Alkaloids Synthesis from Aziridines as Key Advanced Synthetic Intermediates 3.1 Alkylative Aziridine Ring Opening 3.2 Arylative Aziridine Ring Opening 3.3 Ring Expansion 3.4 Oxidative Aziridine Ring Opening 3.5 Heteroatomic Nucleophilic Aziridine Ring Opening 3.6 Reductive Aziridine Ring Opening 4 Conclusion
Key concepts: Aziridine, Chemistry, Ring (chemistry), Nucleophile, Combinatorial chemistry, Organic synthesis, Stereochemistry, Organic chemistry