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dc.contributor.authorSamuel S. Libendi
dc.contributor.authorYosuke Demizu
dc.contributor.authorYoshihiro Matsumura
dc.contributor.authorOsamu Onomura
dc.date.accessioned2012-11-13T16:09:45Z
dc.date.available2012-11-13T16:09:45Z
dc.date.issued2008-04
dc.identifier.citationTetrahedron, Volume 64, Issue 18, 28 April 2008, Pages 3935–3942, http://dx.doi.org/10.1016/j.tet.2008.02.060,en_US
dc.identifier.urihttp://hdl.handle.net/123456789/433
dc.descriptionThe original publication is available at http://www.sciencedirect.com/science/article/pii/S0040402008003219en_US
dc.description.abstractN-Protecting groups of α-substituted cyclicamines strongly affected the regioselectivity in electrochemicalmethoxylation of these compounds. Namely, N-acyl derivatives were transformed into α′-methoxylated compounds, while N-cyano derivatives changed into α-methoxylated derivatives. Furthermore, Lewis acid catalyzed nucleophilic substitution of the α-methoxylated compounds protected with cyano group afforded α,α-disubstituted cyclicamines.en_US
dc.description.sponsorshipPwani Universityen_US
dc.language.isoenen_US
dc.publisherELSELVIERen_US
dc.subjectCyclicamines;en_US
dc.subjectMethoxylation;en_US
dc.subjectElectrochemical oxidationen_US
dc.titleHighregioselectivity in electrochemical α-methoxylation of N-protectedcyclicaminesen_US
dc.typeArticleen_US


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