Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/3108
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dc.contributor.authorAslam, N.A.-
dc.contributor.authorBabu, S.A.-
dc.contributor.authorSingh, Dharmendra Kumar-
dc.contributor.authorRana, A.-
dc.date.accessioned2020-12-14T07:25:01Z-
dc.date.available2020-12-14T07:25:01Z-
dc.date.issued2014-
dc.identifier.citationSynlett, 25(15), pp.2201-2207.en_US
dc.identifier.other10.1055/s-0034-1378517-
dc.identifier.urihttps://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0034-1378517-
dc.identifier.urihttp://hdl.handle.net/123456789/3108-
dc.description.abstractA competent one-pot method comprising magnetically separable nano Fe3O4 catalyzed direct azidation of allylic and benzylic alcohols followed by the copper-catalyzed click reaction of the corresponding azides with alkynes is reported. This method gave a direct access to several 1,2,3-triazoles starting from various allylic and benzylic alcohols via their respective azides.en_US
dc.language.isoenen_US
dc.publisherGeorg Thieme Verlagen_US
dc.subjectAlcoholsen_US
dc.subjectAzidesen_US
dc.subjectClick reactionen_US
dc.subjectCycloadditionen_US
dc.subjectMagnetiteen_US
dc.subjectTriazolesen_US
dc.titleMagnetically Separable Nano Fe3O4 Catalyzed Direct Azidation of Allylic and Benzylic Alcohols Followed by Copper-Catalyzed Click Reactionen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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