STRUCTURAL ELUCIDATION OF BIOACTIVE PRINCIPLES IN FLORAL EXTRACTS OF GERMAN CHAMOMILLE (MATRICARIA RECUTITA L.)
In this work, bioactive compounds present in flower heads of German Chamomille, were extracted and isolated in pure forms by chromatographic techniques. These compounds, spiroketal enol ethers, present in both isomeric forms Z and E, were characterized and unequivocally identified by spectroscopic t...
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Sociedad Chilena de Química
2011
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oai:scielo:S0717-970720110001000062011-06-17STRUCTURAL ELUCIDATION OF BIOACTIVE PRINCIPLES IN FLORAL EXTRACTS OF GERMAN CHAMOMILLE (MATRICARIA RECUTITA L.)BUONO-CORE,G. ENUÑEZ,M. VANESSALUCERO,ANDREAVARGAS M,ROBINSONJULLIAN,CAROLINA Spiroketal enol ethers German Chamomille NMR spectra NOESY In this work, bioactive compounds present in flower heads of German Chamomille, were extracted and isolated in pure forms by chromatographic techniques. These compounds, spiroketal enol ethers, present in both isomeric forms Z and E, were characterized and unequivocally identified by spectroscopic techniques. One- (¹H, 13C) and two-dimensional (¹H-¹H-COSY, ¹H-¹H-NOESY, HMQC and HMBC) NMR were used to assign the configuration of each isomeric compound. It was also found that irradiation of the extracts with UV light induced the photoisomerization of the en-yn-dicycloethers favoring the formation of the more stable E isomer.info:eu-repo/semantics/openAccessSociedad Chilena de QuímicaJournal of the Chilean Chemical Society v.56 n.1 20112011-01-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072011000100006en10.4067/S0717-97072011000100006 |
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Scielo Chile |
language |
English |
topic |
Spiroketal enol ethers German Chamomille NMR spectra NOESY |
spellingShingle |
Spiroketal enol ethers German Chamomille NMR spectra NOESY BUONO-CORE,G. E NUÑEZ,M. VANESSA LUCERO,ANDREA VARGAS M,ROBINSON JULLIAN,CAROLINA STRUCTURAL ELUCIDATION OF BIOACTIVE PRINCIPLES IN FLORAL EXTRACTS OF GERMAN CHAMOMILLE (MATRICARIA RECUTITA L.) |
description |
In this work, bioactive compounds present in flower heads of German Chamomille, were extracted and isolated in pure forms by chromatographic techniques. These compounds, spiroketal enol ethers, present in both isomeric forms Z and E, were characterized and unequivocally identified by spectroscopic techniques. One- (¹H, 13C) and two-dimensional (¹H-¹H-COSY, ¹H-¹H-NOESY, HMQC and HMBC) NMR were used to assign the configuration of each isomeric compound. It was also found that irradiation of the extracts with UV light induced the photoisomerization of the en-yn-dicycloethers favoring the formation of the more stable E isomer. |
author |
BUONO-CORE,G. E NUÑEZ,M. VANESSA LUCERO,ANDREA VARGAS M,ROBINSON JULLIAN,CAROLINA |
author_facet |
BUONO-CORE,G. E NUÑEZ,M. VANESSA LUCERO,ANDREA VARGAS M,ROBINSON JULLIAN,CAROLINA |
author_sort |
BUONO-CORE,G. E |
title |
STRUCTURAL ELUCIDATION OF BIOACTIVE PRINCIPLES IN FLORAL EXTRACTS OF GERMAN CHAMOMILLE (MATRICARIA RECUTITA L.) |
title_short |
STRUCTURAL ELUCIDATION OF BIOACTIVE PRINCIPLES IN FLORAL EXTRACTS OF GERMAN CHAMOMILLE (MATRICARIA RECUTITA L.) |
title_full |
STRUCTURAL ELUCIDATION OF BIOACTIVE PRINCIPLES IN FLORAL EXTRACTS OF GERMAN CHAMOMILLE (MATRICARIA RECUTITA L.) |
title_fullStr |
STRUCTURAL ELUCIDATION OF BIOACTIVE PRINCIPLES IN FLORAL EXTRACTS OF GERMAN CHAMOMILLE (MATRICARIA RECUTITA L.) |
title_full_unstemmed |
STRUCTURAL ELUCIDATION OF BIOACTIVE PRINCIPLES IN FLORAL EXTRACTS OF GERMAN CHAMOMILLE (MATRICARIA RECUTITA L.) |
title_sort |
structural elucidation of bioactive principles in floral extracts of german chamomille (matricaria recutita l.) |
publisher |
Sociedad Chilena de Química |
publishDate |
2011 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072011000100006 |
work_keys_str_mv |
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