Artículos de revistas
Detailed H-1 and C-13 NMR structural assignment and relative stereochemistry determination for three new and one known semi-synthetic sesquiterpene lactones
Fecha
2012Registro en:
JOURNAL OF MOLECULAR STRUCTURE, AMSTERDAM, v. 1008, n. 4, supl. 6, Part 1, pp. 24-28, 45658, 2012
0022-2860
10.1016/j.molstruc.2011.11.012
Autor
Sass, Daiane Cristina
Gomes Heleno, Vladimir Constantino
Ferreira Soares, Ana Carolina
Lopes, Joao Luis Callegari
Constantino, Mauricio Gomes
Institución
Resumen
In this work is described a complete H-1 and C-13 NMR analysis for a group of four sesquiterpene lactones, three previously unknown. The unequivocal assignments were achieved by H-1 NMR, C-13{H-1} NMR, gCOSY. gHMQC, gHMBC and NOESY experiments and no ambiguities were left behind. All hydrogen coupling constants were measured, clarifying all hydrogen signals multiplicities. (C) 2011 Elsevier B.V. All rights reserved.