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dc.contributor.authorGautun, Odd Reidar
dc.contributor.authorCarlsen, Per Henning
dc.date.accessioned2015-09-30T09:07:15Z
dc.date.accessioned2015-11-09T14:30:43Z
dc.date.available2015-09-30T09:07:15Z
dc.date.available2015-11-09T14:30:43Z
dc.date.issued2001
dc.identifier.citationMolecules 2001, 6(12):969-978nb_NO
dc.identifier.issn1420-3049
dc.identifier.urihttp://hdl.handle.net/11250/2359791
dc.description.abstractThe rearrangement of 4-methyl-3,5-diaryl-4H-1,2,4-triazoles to the corresponding 1-methyl-3,5-diaryl-1H-1,2,4-triazoles showed regioselectivity comparable to that observed for the alkylation of 3,5-diaryl-1H-1,2,4-triazoles. This lends support to a proposed mechanism for the rearrangement that involves consecutive nucleophilic displacements steps.nb_NO
dc.language.isoengnb_NO
dc.publisherMDPInb_NO
dc.titleRegioselectivity in the thermal rearrangement of unsymmetrical 4-methyl-4H-1,2,4-triazoles to 1-methyl-1H-1,2,4-triazolesnb_NO
dc.typeJournal articlenb_NO
dc.typePeer revieweden_GB
dc.date.updated2015-09-30T09:07:15Z
dc.source.pagenumber969-978nb_NO
dc.source.volume6nb_NO
dc.source.journalMoleculesnb_NO
dc.source.issue12nb_NO
dc.identifier.doi10.3390/61200969
dc.identifier.cristin409452
dc.description.localcodeThis is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.nb_NO


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