Please use this identifier to cite or link to this item: http://www.repositorio.ufop.br/handle/123456789/7635
Title: Structural determination of 3beta-stearyloxy-urs-12-ene from Maytenus salicifolia by 1D and 2D NMR and quantitative 13C NMR spectroscopy.
Authors: Miranda, Roqueline Rodrigues Silva de
Silva, Gracia Divina de Fátima 
Duarte, Lucienir Pains
Fortes, Isabel Cristina Pereira
Vieira Filho, Sidney Augusto
Keywords: Celastraceae
Issue Date: 2006
Citation: MIRANDA, R. R. S. et al. Structural determination of 3beta-stearyloxy-urs-12-ene from Maytenus salicifolia by 1D and 2D NMR and quantitative 13C NMR spectroscopy. Magnetic Resonance in Chemistry, v. 44, p. 127-131, 2006. Disponível em: <http://onlinelibrary.wiley.com/doi/10.1002/mrc.1734/abstract>. Acesso em: 20 jan. 2017.
Abstract: Six pentacyclic triterpenoids, 3b-stearyloxy-urs-12-ene (1), friedelin (2), 3b-friedelinol (3), a-amyrin (4), b-amyrin (5), and lupeol (6), have been isolated from the hexane extract of Maytenus salicifolia Reissek (Celastraceae) leaves. The molecular and structural formula as well as the stereochemistry of a new pentacyclic triterpene (1) were determined using data obtained from 1H and 13C NMR spectra, DEPT135 and by 2D HSQC, HMBC, COSY and NOESY experiments. The molecular formula C48H84O2 was established using quantitative 13C NMR, and the molecular weight (692 Da) was confirmed by elemental analysis and mass spectrometry (GC-MS).
URI: http://www.repositorio.ufop.br/handle/123456789/7635
metadata.dc.identifier.uri2: http://onlinelibrary.wiley.com/doi/10.1002/mrc.1734/abstract
ISSN: 1097458X
Appears in Collections:DEFAR - Artigos publicados em periódicos

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