Palladium-catalyzed tandem reaction of 2-chloroquinoline-3-carbaldehydes and isocyanides

A facile domino reaction of 2-chloroquinoline-3-carbaldehydes in one and two equivalents of isocyanide has been investigated. Three-component reactions of 2-chloroquinoline-3-carbaldehydes, isocyanides and amines are also described. In this Pd-catalyzed reaction under controlled conditions, three no...

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Veröffentlicht in:Organic & biomolecular chemistry 2017, Vol.15 (47), p.10073-10081
Hauptverfasser: Shiri, Morteza, Ranjbar, Maryam, Yasaei, Zahra, Zamanian, Fatemeh, Notash, Behrouz
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Sprache:eng
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Zusammenfassung:A facile domino reaction of 2-chloroquinoline-3-carbaldehydes in one and two equivalents of isocyanide has been investigated. Three-component reactions of 2-chloroquinoline-3-carbaldehydes, isocyanides and amines are also described. In this Pd-catalyzed reaction under controlled conditions, three novel types of quinoline derivatives were formed via amidation, lactamization or carbamate formation along with the formation of C-C, C-N, and C-O bonds in a one-pot procedure.
ISSN:1477-0520
1477-0539
DOI:10.1039/c7ob02043k