Acid-Catalyzed 1,3-Dipolar Cycloaddition of 2H-Azirines with Nitrones: An Unexpected Access to 1,2,4,5-Tetrasubstituted Imidazoles
Author:
Affiliation:
1. AVIDIN Ltd., Alsó kikötő sor 11/D, Szeged H-6726, Hungary
2. Department of Organic Chemistry, University of Szeged, Dóm tér 8, H-6720 Szeged, Hungary
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b03288
Reference78 articles.
1. 2H-Azirines as Synthetic Tools in Organic Chemistry
2. PREPARATION, PROPERTIES AND SYNTHETIC APPLICATIONS OF 2H-AZIRINES A REVIEW
3. Lewis Acid-Catalyzed Diastereoselective Synthesis of Multisubstituted N-Acylaziridine-2-carboxamides from 2H-Azirines via Joullié–Ugi Three-Component Reaction
4. Enantioselective Reaction of 2 H ‐Azirines
5. Modular 2,3-diaryl-2H-azirine synthesis from ketoxime acetates via Cs2CO3-mediated cyclization
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