Catalytic Asymmetric Synthesis of Atropisomeric N‑Aryl 1,2,4-Triazoles

The atroposelective synthesis of N-aryl 1,2,4-triazoles was developed. A cyclodehydration reaction was rendered asymmetric with the use of a chiral phosphoric acid catalyst to afford atropisomeric N-aryl 1,2,4-triazoles in up to 91:9 er. Recrystallization of the isolated heterocycle further enriched...

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Veröffentlicht in:Journal of organic chemistry 2023-06, Vol.88 (12), p.7815-7820
Hauptverfasser: Choi, Sooyun, Guo, Melody C., Coombs, Gavin M., Miller, Scott J.
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Sprache:eng
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Zusammenfassung:The atroposelective synthesis of N-aryl 1,2,4-triazoles was developed. A cyclodehydration reaction was rendered asymmetric with the use of a chiral phosphoric acid catalyst to afford atropisomeric N-aryl 1,2,4-triazoles in up to 91:9 er. Recrystallization of the isolated heterocycle further enriched the atropisomeric ratio of several analogs to 99:1 er or greater. A divergent and substrate-dependent reaction pathway yielding a different heterocyclic product is also disclosed.
ISSN:0022-3263
1520-6904
DOI:10.1021/acs.joc.2c02727