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spelling paper:paper_01633864_v72_n10_p1902_Maier2023-06-08T15:14:18Z Fernene triterpenoids from the lichen Pyxine berteriana Maier, Marta Silvia Rosso, María Luciana Fazio, Alejandra Teresa Adler, Monica Teresa Bertoni, María Delia Luisa 3beta acetoxyfern 9(11) en 19 one 3beta acetoxyfern 9(11) en 19beta ol acetone fern 9(11) en 3,19 dione fernene triterpenoid derivative lichexanthone triterpenoid unclassified drug article Ascomycetes chemical structure controlled study infrared radiation isolation procedure nuclear magnetic resonance Pyxine berteriana structure analysis Argentina Lichens Molecular Structure Nuclear Magnetic Resonance, Biomolecular Structure-Activity Relationship Triterpenes Filicophyta Pyxine berteriana Two new fernene triterpenoids, fern-9(11)-en-3,19-dione (1) and 3β-acetoxyfern-9(11)-en-19-one (2), together with the known 3β-acetoxyfern-9(11)-en-19β-ol (3) and lichexanthone (4), have been isolated from the acetone extract of the lichen Pyxine berteriana. The structures of the new compounds were established on the basis of IR, extensive 1D and 2D NMR, and MS analyses. Although several fern-9(11)-enes have been isolated from lichens, compounds 1 and 2 are the first examples of naturally occurring fernene triterpenoids with a carbonyl function at C-19. © 2009 American Chemical Society and American Society of Pharmacognosy. Fil:Maier, M.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Rosso, M.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Fazio, A.T. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Adler, M.T. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Bertoni, M.D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2009 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01633864_v72_n10_p1902_Maier http://hdl.handle.net/20.500.12110/paper_01633864_v72_n10_p1902_Maier
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 3beta acetoxyfern 9(11) en 19 one
3beta acetoxyfern 9(11) en 19beta ol
acetone
fern 9(11) en 3,19 dione
fernene triterpenoid derivative
lichexanthone
triterpenoid
unclassified drug
article
Ascomycetes
chemical structure
controlled study
infrared radiation
isolation procedure
nuclear magnetic resonance
Pyxine berteriana
structure analysis
Argentina
Lichens
Molecular Structure
Nuclear Magnetic Resonance, Biomolecular
Structure-Activity Relationship
Triterpenes
Filicophyta
Pyxine berteriana
spellingShingle 3beta acetoxyfern 9(11) en 19 one
3beta acetoxyfern 9(11) en 19beta ol
acetone
fern 9(11) en 3,19 dione
fernene triterpenoid derivative
lichexanthone
triterpenoid
unclassified drug
article
Ascomycetes
chemical structure
controlled study
infrared radiation
isolation procedure
nuclear magnetic resonance
Pyxine berteriana
structure analysis
Argentina
Lichens
Molecular Structure
Nuclear Magnetic Resonance, Biomolecular
Structure-Activity Relationship
Triterpenes
Filicophyta
Pyxine berteriana
Maier, Marta Silvia
Rosso, María Luciana
Fazio, Alejandra Teresa
Adler, Monica Teresa
Bertoni, María Delia Luisa
Fernene triterpenoids from the lichen Pyxine berteriana
topic_facet 3beta acetoxyfern 9(11) en 19 one
3beta acetoxyfern 9(11) en 19beta ol
acetone
fern 9(11) en 3,19 dione
fernene triterpenoid derivative
lichexanthone
triterpenoid
unclassified drug
article
Ascomycetes
chemical structure
controlled study
infrared radiation
isolation procedure
nuclear magnetic resonance
Pyxine berteriana
structure analysis
Argentina
Lichens
Molecular Structure
Nuclear Magnetic Resonance, Biomolecular
Structure-Activity Relationship
Triterpenes
Filicophyta
Pyxine berteriana
description Two new fernene triterpenoids, fern-9(11)-en-3,19-dione (1) and 3β-acetoxyfern-9(11)-en-19-one (2), together with the known 3β-acetoxyfern-9(11)-en-19β-ol (3) and lichexanthone (4), have been isolated from the acetone extract of the lichen Pyxine berteriana. The structures of the new compounds were established on the basis of IR, extensive 1D and 2D NMR, and MS analyses. Although several fern-9(11)-enes have been isolated from lichens, compounds 1 and 2 are the first examples of naturally occurring fernene triterpenoids with a carbonyl function at C-19. © 2009 American Chemical Society and American Society of Pharmacognosy.
author Maier, Marta Silvia
Rosso, María Luciana
Fazio, Alejandra Teresa
Adler, Monica Teresa
Bertoni, María Delia Luisa
author_facet Maier, Marta Silvia
Rosso, María Luciana
Fazio, Alejandra Teresa
Adler, Monica Teresa
Bertoni, María Delia Luisa
author_sort Maier, Marta Silvia
title Fernene triterpenoids from the lichen Pyxine berteriana
title_short Fernene triterpenoids from the lichen Pyxine berteriana
title_full Fernene triterpenoids from the lichen Pyxine berteriana
title_fullStr Fernene triterpenoids from the lichen Pyxine berteriana
title_full_unstemmed Fernene triterpenoids from the lichen Pyxine berteriana
title_sort fernene triterpenoids from the lichen pyxine berteriana
publishDate 2009
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01633864_v72_n10_p1902_Maier
http://hdl.handle.net/20.500.12110/paper_01633864_v72_n10_p1902_Maier
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AT rossomarialuciana fernenetriterpenoidsfromthelichenpyxineberteriana
AT fazioalejandrateresa fernenetriterpenoidsfromthelichenpyxineberteriana
AT adlermonicateresa fernenetriterpenoidsfromthelichenpyxineberteriana
AT bertonimariadelialuisa fernenetriterpenoidsfromthelichenpyxineberteriana
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