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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/2867
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dc.contributor.authorKumar, Anil-
dc.date.accessioned2021-10-17T13:57:06Z-
dc.date.available2021-10-17T13:57:06Z-
dc.date.issued2015-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2015/OB/C4OB02375G-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2867-
dc.description.abstractAn efficient one-pot sequential procedure is described for the synthesis of novel azole-fused quinazolines through Pd/Cu co-catalyzed, Ullmann-type coupling followed by cross dehydrogenative coupling of various azoles such as 1H-imidazole, 1H-benzimidazole and 1H-1,2,4-triazole with 2-(2-bromophenyl)-1H-imidazole/benzimidazoles. The developed strategy has offered good yields (52–81%) of diverse N-fused tetra-, penta- and hexa-cyclic frameworks in a single stepen_US
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectSynthesisen_US
dc.subjectC–N bondingen_US
dc.titleSynthesis of novel azole-fused quinazolines via one-pot, sequential Ullmann-type coupling and intramolecular dehydrogenative C–N bondingen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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