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dc.contributor.authorOnomura, Osamu
dc.contributor.authorDemizu, Yosuke
dc.contributor.authorMatsumura, Yoshihiro
dc.contributor.authorS. Libendi, Samuel
dc.date.accessioned2012-11-13T15:47:44Z
dc.date.available2012-11-13T15:47:44Z
dc.date.issued2009-01
dc.identifier.citationHeterocycles, 77 (1), pp.311-321; 2009, 10.3987/COM-08-S(F)18en_US
dc.identifier.issn03855414
dc.identifier.urihttp://hdl.handle.net/123456789/432
dc.descriptionThe original publication is available at http://naosite.lb.nagasaki-u.ac.jp/dspace/handle/10069/21990en_US
dc.description.abstractα,β-Unsaturated cyclic amines are oxidized by OsO4 to afford α,β-cis-dihydroxylated compounds which are thermodynamically transformed into ring-opened keto-alcohols. The keto-alcohols are then cyclized to form synthetically useful ring-contracted cyclic amines.en_US
dc.description.sponsorshipPwani Universityen_US
dc.language.isoenen_US
dc.publisherThe Japan Institute of Heterocyclic Chemistryen_US
dc.subjectRing Contractionen_US
dc.subjectUnsaturated Cyclicen_US
dc.subjectcis-Dihydroxylationen_US
dc.titleRing Contraction of α,β-Unsaturated Cyclic Amines with cis-Dihydroxylation at the α,β-Positionen_US
dc.typeArticleen_US


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