Structure And Absolute Stereochemistry Of Pseudorepanduline. 13c-nmr Studies On Repanduline-type Alkaloids

dc.creatorKoike L.
dc.creatorReis F.D.A.M.
dc.creatorBick I.R.C.
dc.date1992
dc.date2015-06-30T14:20:47Z
dc.date2015-11-26T14:42:51Z
dc.date2015-06-30T14:20:47Z
dc.date2015-11-26T14:42:51Z
dc.date.accessioned2018-03-28T21:50:39Z
dc.date.available2018-03-28T21:50:39Z
dc.identifier
dc.identifierJournal Of Natural Products. , v. 55, n. 4, p. 455 - 460, 1992.
dc.identifier1633864
dc.identifier
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-0026631375&partnerID=40&md5=e3a0f88f46817d462a6da54222d29482
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/99404
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/99404
dc.identifier2-s2.0-0026631375
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1251440
dc.descriptionThe 13C-nmr spectrum of repanduline was assigned from the known structure 2 by means of 13C-1H (HETCOR) 2D correlation experiments. Using data from repanduline in conjunction with 1H-1H (COSY) and HETCOR 2D studies on pseudorepanduline [1], the absolute stereochemistry of 1 has been determined. Some observations are made on the conformation of repanduline-type alkaloids and on their possible mode of biosynthesis.
dc.description55
dc.description4
dc.description455
dc.description460
dc.languageen
dc.publisher
dc.relationJournal of Natural Products
dc.rightsfechado
dc.sourceScopus
dc.titleStructure And Absolute Stereochemistry Of Pseudorepanduline. 13c-nmr Studies On Repanduline-type Alkaloids
dc.typeArtículos de revistas


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