Please use this identifier to cite or link to this item: http://dspace.iitrpr.ac.in:8080/xmlui/handle/123456789/3868
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dc.contributor.authorBhatt, D.-
dc.contributor.authorSingh, P.R.-
dc.contributor.authorKalaramna, P.-
dc.contributor.authorKumar, K.-
dc.contributor.authorGoswami, A.-
dc.date.accessioned2022-08-23T10:42:18Z-
dc.date.available2022-08-23T10:42:18Z-
dc.date.issued2022-08-23-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/3868-
dc.description.abstractAn efficient method to access 2-triazolyl thio-/selenopyridines with good to excellent yields by ruthenium(II)-catalyzed one-pot [3+2]/[2+2+2] cycloaddition reactions of azides, 1-alkynyl thio-/selenocyanates and 1,6-diynes is reported. This atom-economical catalytic strategy offers a mild and practical approach to access a variety of such cycloadducts with good to excellect regioselectivities. The protocol was further extended to the synthesis of 3,3′-bis(triazolyl thio-/seleno)-2,2′-bipyridines by the reaction of tetraynes with 1-alkynyl thio-/selenocyanates in the presence of aryl/alkyl azidesen_US
dc.language.isoen_USen_US
dc.subjectcyclotrimerizationsen_US
dc.subjectruthenium catalysisen_US
dc.subjectThio-/seleno substituted triazolesen_US
dc.subjecttriazolyl thio-/selenopyridinesen_US
dc.subject[3+2] cycloadditionsen_US
dc.titleAn Atom-Economical Approach to 2-Triazolyl Thio-/Seleno Pyridines via Ruthenium-Catalyzed One-pot [3+2]/[2+2+2] Cycloadditionsen_US
dc.typeArticleen_US
Appears in Collections:Year-2019

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