Please use this identifier to cite or link to this item: http://dspace.iitrpr.ac.in:8080/xmlui/handle/123456789/2430
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dc.contributor.authorKalaramna, P.-
dc.contributor.authorBhatt, D.-
dc.contributor.authorSharma, H.-
dc.contributor.authorGoswami, A.-
dc.date.accessioned2021-08-19T23:28:01Z-
dc.date.available2021-08-19T23:28:01Z-
dc.date.issued2021-08-20-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/2430-
dc.description.abstractA highly efficient protocol for the synthesis of 2-aryl/ hetero aryl selenopyridines has been developed via a ruthenium(II)-catalyzed cycloaddition reaction of 1,6-diynes with aryl/heteroaryl selenocyanates with good to excellent yields. It was found that various diynes and selenocyanates expediently underwent the reaction under open-flask conditions. This atomeconomical catalytic strategy offers a mild and practical approach to access a variety of such cycloadducts with excellent regioselectivities.en_US
dc.language.isoen_USen_US
dc.titleAn expeditious and environmentally-benign approach to 2-aryl/heteroaryl selenopyridines via ruthenium catalyzed [2+2+2] cycloadditionsen_US
dc.typeArticleen_US
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