A copper(ii)-catalyzed annulative formylation of o -alkynylanilines with DMF: a single-step strategy for 3-formyl indoles
In this paper, a copper(ii)-catalyzed reaction of -alkynylanilines with dimethylformamide (DMF) in the presence of oxygen has been developed for synthesizing multisubstituted 3-formyl indole scaffolds. This one-pot reaction proceeds through a cascade 5- -dig cyclization followed by formylation to co...
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Veröffentlicht in: | RSC advances 2018-01, Vol.8 (71), p.40968-40973 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | In this paper, a copper(ii)-catalyzed reaction of
-alkynylanilines with dimethylformamide (DMF) in the presence of oxygen has been developed for synthesizing multisubstituted 3-formyl indole scaffolds. This one-pot reaction proceeds through a cascade 5-
-dig cyclization followed by formylation to construct 1,2-disubstituted 3-formyl indoles. The key aspects of this synthesis method are the broad substrate scope (with 38 examples), and well tolerating various functional groups. In addition, a detailed mechanism has been proposed, where DMF may serve as a carbon source for the
C3 formylation of the obtained indole derivatives. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/c8ra09214a |