Please use this identifier to cite or link to this item:
Type: Artigo de periódico
Title: Structure And Absolute Stereochemistry Of Pseudorepanduline. 13c-nmr Studies On Repanduline-type Alkaloids
Author: Koike L.
Reis F.D.A.M.
Bick I.R.C.
Abstract: The 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.
Citation: Journal Of Natural Products. , v. 55, n. 4, p. 455 - 460, 1992.
Rights: fechado
Identifier DOI: 
Date Issue: 1992
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File SizeFormat 
2-s2.0-0026631375.pdf351.93 kBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.