Aminoalkylation of nitriles by iminium ions generated in situ

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dc.contributor.authorKatritzky, A.R.
dc.contributor.authorAbdel-Fattah, A.A.A.
dc.contributor.authorSteel, P.J.
dc.date.accessioned2007-08-17T00:39:03Z
dc.date.available2007-08-17T00:39:03Z
dc.date.issued2006en
dc.description.abstractAminoalkylation of a series of primary and secondary nitriles with N-(α-aminoalkyl)benzotriazoles 1 (derived from a variety of secondary amines and aldehydes) proceeds smoothly providing the corresponding β-aminoalkyl nitriles 5a–j in 66–97% yields.en
dc.identifier.citationKatritzky, A.R., Abdel-Fattah, A.A.A, Steel, P.J. (2006) Aminoalkylation of nitriles by iminium ions generated in situ. Tetrahedron Letters, 47(9), pp. 1465-1467.en
dc.identifier.doihttps://doi.org/10.1016/j.tetlet.2005.12.059
dc.identifier.issn0040-4039
dc.identifier.urihttp://hdl.handle.net/10092/379
dc.language.isoen
dc.publisherUniversity of Canterbury. Chemistry.en
dc.rights.urihttps://hdl.handle.net/10092/17651en
dc.subjectAminoalkylationen
dc.subjectN-(α-Aminoalkyl)benzotriazolesen
dc.subjectß-Aminoalkyl nitrilesen
dc.subject.marsdenFields of Research::250000 Chemical Sciences::250300 Organic Chemistry::250301 Organic chemical synthesisen
dc.titleAminoalkylation of nitriles by iminium ions generated in situen
dc.typeJournal Article
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