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dc.contributor.authorFARIBA HEIDARIZADEH-
dc.contributor.authorAMANOLAH ZAREI-
dc.date.accessioned2023-12-08T04:24:53Z-
dc.date.available2023-12-08T04:24:53Z-
dc.date.issued2012-06-20-
dc.identifier.citationHeidarizadeh, F., & Zarei, A. (2012). Bronsted acidic ionic liquid 1-n-butylimidazolium tetrafluoroborate ([hbim] bf4): A green catalyst and recyclable medium for the azidolysis of epoxides. J. Chem. Soc. Pak, 34(3), 593.en_US
dc.identifier.issn0253-5106-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/20007-
dc.description.abstractEpoxides undergo rapidly ring opening with sodium azide in [Hbim]BF4/H2O (2:1) medium, under mild condition to afford the corresponding 2-azidoalchols in high yields. The remarkable features of this procedure are improved yields, enhanced reaction rates, regiospecify and ease of recyclability of ionic liquids (ILs). The recovered ionic liquid can be reused for five times but with only a gradual decrease in activity observed.en_US
dc.description.sponsorshipThe chemical society of Pakistan is an approved society from the PSF.en_US
dc.language.isoenen_US
dc.publisherHEJ Research Institute of Chemistry, University of Karachi, Karachi.en_US
dc.subjectProtic ionic liquiden_US
dc.subjectEpoxideen_US
dc.subject2-Azidoalcoholsen_US
dc.subjectAzidolysisen_US
dc.subjectRing openingen_US
dc.titleBrønsted Acidic Ionic Liquid 1-n-butylimidazolium tetrafluoroborate ([hbim]bf4): A Green Catalyst and Recyclable Medium for the Azidolysis of Epoxidesen_US
dc.typeArticleen_US
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