Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2860
Full metadata record
DC FieldValueLanguage
dc.contributor.authorDhiman, Seema-
dc.contributor.authorRamasastry, S.S.V.-
dc.date.accessioned2020-12-09T05:34:40Z-
dc.date.available2020-12-09T05:34:40Z-
dc.date.issued2013-
dc.identifier.citationOrganic and Biomolecular Chemistry, 11(26), pp. 4299-4303.en_US
dc.identifier.otherhttps://doi.org/10.1039/C3OB40814K-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2013/ob/c3ob40814k#!divAbstract-
dc.identifier.urihttp://hdl.handle.net/123456789/2860-
dc.description.abstractFurfuryl cations are generated via a highly efficient bismuth-catalyzed reaction of furfuryl alcohols. This systematic study provides insight on the reactivity profile of furfuryl cations towards nucleophilic substitution reactions. Novel C-C, C-N, C-O and C-S bond forming reactions of furfuryl cations have been developed, thus providing access to a diverse array of building blocks for further manipulations.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectFurfuryl cationsen_US
dc.subjectAlcoholsen_US
dc.subjectHighly efficient bismuth-catalyzeden_US
dc.titleTaming furfurylcations for the synthesis of privileged structures and novel scaffolds†‡en_US
dc.typeArticleen_US
Appears in Collections:Research Articles

Files in This Item:
File Description SizeFormat 
Need to add pdf.odt8.63 kBOpenDocument TextView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.