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dc.contributor.authorKalaramna, P.-
dc.contributor.authorBhatt, D.-
dc.contributor.authorSharma, H.-
dc.contributor.authorGoswami, A.-
dc.date.accessioned2019-12-11T17:02:35Z-
dc.date.available2019-12-11T17:02:35Z-
dc.date.issued2019-12-11-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/1423-
dc.description.abstractAn efficient, ruthenium(II)-catalyzed, solvent-free approach for the synthesis of 2-aryloxypyridines with good to excellent yields has been developed by the reaction of 1,6-diynes with aryl cyanates. This atom-economical catalytic strategy offers a mild and practical approach to access a variety of such cycloadducts with excellent regioselectivities. The protocol was further extended to the synthesis of 2,2’- and 2,3’-diaryloxybipyridines by the reaction of tetraynes with aryl cyanates.en_US
dc.language.isoen_USen_US
dc.subject2-aryloxypyridinesen_US
dc.subject2,2’- & 2,3’-diaryloxy bipyridinesen_US
dc.subjectRuthenium catalysten_US
dc.subject[2+2+2] cycloadditionen_US
dc.subjectSolvent-freeen_US
dc.titleAn atom-economical approach to 2-aryloxypyridines and 2,2’/2,3’-diaryloxybipyridines via ruthenium-catalyzed [2 + 2 + 2] cycloadditionsen_US
dc.typeArticleen_US
Appears in Collections:Year-2019

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