Pyrimidines as Surrogates for 1,3‐Dicarbonyl Compounds in peri Annulation of Perimidines en Route to 1,3‐Diazapyrenes

A highly efficient protocol for acid‐mediated peri annulation of perimidines with pyrimidines has been developed. Pyrimidines, used as surrogates for 1,3‐dicarbonyl compounds, furnish benzo[gh]perimidines, which includes hardly available analogues, non‐substituted, or mono‐substituted at C‐6, C‐8. L...

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Veröffentlicht in:European journal of organic chemistry 2017-03, Vol.2017 (12), p.1666-1673
Hauptverfasser: Aksenov, Alexander V., Shcherbakov, Stanisvlav V., Lobach, Irina V., Aksenova, Inna V., Rubin, Michael
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Sprache:eng
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Zusammenfassung:A highly efficient protocol for acid‐mediated peri annulation of perimidines with pyrimidines has been developed. Pyrimidines, used as surrogates for 1,3‐dicarbonyl compounds, furnish benzo[gh]perimidines, which includes hardly available analogues, non‐substituted, or mono‐substituted at C‐6, C‐8. Limitations of reactions that use 5‐bromopyrimidines are investigated. A highly efficient protocol for acid‐mediated peri annulation of perimidines with pyrimidines has been developed. Pyrimidines, used as surrogates for 1,3‐dicarbonyl compounds, furnish benzo[gh]perimidines, which includes hardly available analogues, non‐substituted, or mono‐substituted at C‐6, C‐8.
ISSN:1434-193X
1099-0690
DOI:10.1002/ejoc.201601589