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Data from: Structure and Absolute Configuration of Diterpenoids from Hymenaea stigonocarpa

RMIT University, Australia
Ewan Blanch (Aggregated by)
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ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2FANDS&rft_id=https://figshare.com/articles/Structure_and_Absolute_Configuration_of_Diterpenoids_from_i_Hymenaea_stigonocarpa_i_/2154724&rft.title=Data from: Structure and Absolute Configuration of Diterpenoids from Hymenaea stigonocarpa&rft.identifier=71394f5b63110f987d8967127c55d3b6&rft.publisher=RMIT University, Australia&rft.description=Attached file provides supplementary data for linked article. 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 H-1 and C-13 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.&rft.creator=Ewan Blanch&rft.date=2018&rft.relation=http://dx.doi.org/10.1021/acs.jnatprod.5b00166&rft_rights=All rights reserved&rft_rights=CC BY-NC: Attribution-Noncommercial 3.0 AU http://creativecommons.org/licenses/by-nc/3.0/au&rft_subject=Raman optical activity &rft_subject=Vibrational circular dichroism&rft_subject=Medicinal plant&rft_subject=Spectroscopy&rft_subject=Stereochemistry &rft_subject=Lepidopteran&rft_subject=Physical Chemistry not elsewhere classified&rft_subject=CHEMICAL SCIENCES&rft_subject=PHYSICAL CHEMISTRY (INCL. STRUCTURAL)&rft.type=dataset&rft.language=English Access the data
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Attached file provides supplementary data for linked article. 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 H-1 and C-13 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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Chemical Sciences | Lepidopteran | Medicinal plant | Physical Chemistry (Incl. Structural) | Physical Chemistry Not Elsewhere Classified | Raman optical activity | Spectroscopy | Stereochemistry | Vibrational circular dichroism |

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