Structure and absolute configuration of diterpenoids from hymenaea stigonocarpa
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Data
2015-06-01
Autores
Monteiro, Afif F.
Batista, Joao M. [UNESP]
Machado, Michelle A.
Severino, Richele P.
Blanch, Ewan W.
Bolzani, Vanderlan da Silva [UNESP]
Vieira, Paulo C.
Severino, Vanessa G. P.
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Amer Chemical Soc
Resumo
Chemical investigations of the ethanolic extracts from the flowers and leaves of Hymenaea stigonocarpa Mart. ex Hayne afforded one new ent-halimane diterpenoid, 18-hydroxy-ent-halima-1(10),13-(E)-dien-15-oic acid (1), together with five known compounds (2-6). The structural elucidation was performed by means of NMR (COSY, HSQC, HMBC, and NOESY) and MS analyses. Complete ¹H and ¹³C NMR data assignments are also reported for labd-13-en-8 beta-ol-15-oic (2) and labd-7,13-dien-15-oic (3) acids. The absolute configurations of 1 and 2 were established by comparison of experimental and calculated Raman optical activity spectra.
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Journal Of Natural Products. Washington: Amer Chemical Soc, v. 78, n. 6, p. 1451-1455, 2015.