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A one-pot,two-step synthesis of 3-deazacanthin-4-ones via sequential Pd-catalyzed Suzuki-Miyaura and Cu-catalyzed Buchwald-Hartwig reactions
Authors:Emmanouil Broumidis  Panayiotis A. Koutentis
Affiliation:Department of Chemistry, University of Cyprus, P. O. Box 20537, 1678 Nicosia, Cyprus
Abstract:3-Deazacanthin-4-one and nine analogues, including the 8-aza analogue, were prepared rapidly and in high yields from 8-iodoquinolones and 2-chloro(het)arylboronic acids. The strategy involves construction of the central B ring via concomitant Pd-catalyzed Suzuki-Miyaura C/>C and Cu-catalyzed Buchwald-Hartwig C<img style=
Keywords:Canthine alkaloids  Nitrogen heterocycles  Suzuki-Miyaura reaction  Buchwald-Hartwig reaction  Transition-metal catalysis
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