Chemical constituents from Ouratea floribunda: complete 1H and 13C NMR assignments of atranorin and its new acetyl derivative

Chromatographic fractionation of the hexane extract from the wood of Ouratea floribunda (Ochnaceae) afforded friedelin (1), friedelanol (2), lupeol (3) and the depside atranorin (4). The structure elucidation of the isolated compounds was performed by spectrometric analysis involving comparison with...

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Main Authors: Carvalho Mário G. de, Carvalho Geizi J. A. de, Braz-Filho Raimundo
Format: Article
Language:English
Published: Sociedade Brasileira de Química 2000-01-01
Series:Journal of the Brazilian Chemical Society
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532000000200007
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author Carvalho Mário G. de
Carvalho Geizi J. A. de
Braz-Filho Raimundo
author_facet Carvalho Mário G. de
Carvalho Geizi J. A. de
Braz-Filho Raimundo
author_sort Carvalho Mário G. de
collection DOAJ
description Chromatographic fractionation of the hexane extract from the wood of Ouratea floribunda (Ochnaceae) afforded friedelin (1), friedelanol (2), lupeol (3) and the depside atranorin (4). The structure elucidation of the isolated compounds was performed by spectrometric analysis involving comparison with literature data. The unambiguous assignments of ¹H and 13C NMR data of atranorin 4 and its acetyl derivative 4a are reported for the first time and involved ¹H-¹H homonuclear (COSY and NOESY) and ¹H-13C heteronuclear (HMQC and HMBC) NMR experiments.
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spelling doaj.art-d64f3cc155b447898761551848eb852a2022-12-21T23:29:59ZengSociedade Brasileira de QuímicaJournal of the Brazilian Chemical Society0103-50532000-01-01112143147Chemical constituents from Ouratea floribunda: complete 1H and 13C NMR assignments of atranorin and its new acetyl derivativeCarvalho Mário G. deCarvalho Geizi J. A. deBraz-Filho RaimundoChromatographic fractionation of the hexane extract from the wood of Ouratea floribunda (Ochnaceae) afforded friedelin (1), friedelanol (2), lupeol (3) and the depside atranorin (4). The structure elucidation of the isolated compounds was performed by spectrometric analysis involving comparison with literature data. The unambiguous assignments of ¹H and 13C NMR data of atranorin 4 and its acetyl derivative 4a are reported for the first time and involved ¹H-¹H homonuclear (COSY and NOESY) and ¹H-13C heteronuclear (HMQC and HMBC) NMR experiments.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532000000200007Ouratea floribundaOchnaceaeatranorinmonoacetylatranorin
spellingShingle Carvalho Mário G. de
Carvalho Geizi J. A. de
Braz-Filho Raimundo
Chemical constituents from Ouratea floribunda: complete 1H and 13C NMR assignments of atranorin and its new acetyl derivative
Journal of the Brazilian Chemical Society
Ouratea floribunda
Ochnaceae
atranorin
monoacetylatranorin
title Chemical constituents from Ouratea floribunda: complete 1H and 13C NMR assignments of atranorin and its new acetyl derivative
title_full Chemical constituents from Ouratea floribunda: complete 1H and 13C NMR assignments of atranorin and its new acetyl derivative
title_fullStr Chemical constituents from Ouratea floribunda: complete 1H and 13C NMR assignments of atranorin and its new acetyl derivative
title_full_unstemmed Chemical constituents from Ouratea floribunda: complete 1H and 13C NMR assignments of atranorin and its new acetyl derivative
title_short Chemical constituents from Ouratea floribunda: complete 1H and 13C NMR assignments of atranorin and its new acetyl derivative
title_sort chemical constituents from ouratea floribunda complete 1h and 13c nmr assignments of atranorin and its new acetyl derivative
topic Ouratea floribunda
Ochnaceae
atranorin
monoacetylatranorin
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532000000200007
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