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
Hauptverfasser: Ganesan, Balaji, Senadi, Gopal Chandru, Guo, Bing-Chun, Hung, Min-Yuan, Lin, Wei-Yu
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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.
ISSN:2046-2069
2046-2069
DOI:10.1039/c8ra09214a