Rh(iii)-catalyzed sequential C-H activation and annulation: access to N-fused heterocycles from arylazoles and α-diazocarbonyl compoundsElectronic supplementary information (ESI) available. See DOI: 10.1039/c7ra03262e
A mild and simple protocol has been developed for the synthesis of N-fused heterocycles from arylazoles and α-diazocarbonyl compounds via Rh( iii )-catalyzed sequential C-H activation and annulation. Three kinds of N-fused heterocycles derived from arylpyrazoles, arylbenzimidazoles and aryl 1,2,4-tr...
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A mild and simple protocol has been developed for the synthesis of N-fused heterocycles from arylazoles and α-diazocarbonyl compounds
via
Rh(
iii
)-catalyzed sequential C-H activation and annulation. Three kinds of N-fused heterocycles derived from arylpyrazoles, arylbenzimidazoles and aryl 1,2,4-triazole were successfully obtained. The reactivity of the other four arylazole analogues was also investigated.
Valuable N-fused heterocycles were successfully obtained
via
Rh(
iii
)-catalyzed sequential C-H activation and annulation. |
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ISSN: | 2046-2069 |
DOI: | 10.1039/c7ra03262e |