A new rearranged dolabellane diterpene from the soft coral Clavularia inflata
A new dolabellane type diterpene 1 has been isolated through its acetate 1a. The structure of 1a was elucidated by extensive 1D and 2D NMR spectroscopy and confirmed by mass spectrometry. The structure of 1 was deduced by comparison of its NMR spectral data with those of 1a, while its relative stere...
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oai:animorepository.dlsu.edu.ph:faculty_research-21452024-03-25T00:16:06Z A new rearranged dolabellane diterpene from the soft coral Clavularia inflata Alea, Glenn V. Bowden, Bruce F. Ragasa, Consolacion Y. A new dolabellane type diterpene 1 has been isolated through its acetate 1a. The structure of 1a was elucidated by extensive 1D and 2D NMR spectroscopy and confirmed by mass spectrometry. The structure of 1 was deduced by comparison of its NMR spectral data with those of 1a, while its relative stereochemistry was deduced by NOESY. The absolute stereochemistry of C-7 was determined by analyses of 1 separately esterified with R and S O-mandelic acids. 2008-06-15T07:00:00Z text text/html https://animorepository.dlsu.edu.ph/faculty_research/1146 info:doi/10.1080/14786410701640528 https://animorepository.dlsu.edu.ph/context/faculty_research/article/2145/type/native/viewcontent/14786410701640528.html Faculty Research Work Animo Repository Diterpenes Alcyonacea—Analysis Chemistry |
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De La Salle University |
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De La Salle University Library |
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Asia |
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Philippines Philippines |
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DLSU Institutional Repository |
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Diterpenes Alcyonacea—Analysis Chemistry |
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Diterpenes Alcyonacea—Analysis Chemistry Alea, Glenn V. Bowden, Bruce F. Ragasa, Consolacion Y. A new rearranged dolabellane diterpene from the soft coral Clavularia inflata |
| description |
A new dolabellane type diterpene 1 has been isolated through its acetate 1a. The structure of 1a was elucidated by extensive 1D and 2D NMR spectroscopy and confirmed by mass spectrometry. The structure of 1 was deduced by comparison of its NMR spectral data with those of 1a, while its relative stereochemistry was deduced by NOESY. The absolute stereochemistry of C-7 was determined by analyses of 1 separately esterified with R and S O-mandelic acids. |
| format |
text |
| author |
Alea, Glenn V. Bowden, Bruce F. Ragasa, Consolacion Y. |
| author_facet |
Alea, Glenn V. Bowden, Bruce F. Ragasa, Consolacion Y. |
| author_sort |
Alea, Glenn V. |
| title |
A new rearranged dolabellane diterpene from the soft coral Clavularia inflata |
| title_short |
A new rearranged dolabellane diterpene from the soft coral Clavularia inflata |
| title_full |
A new rearranged dolabellane diterpene from the soft coral Clavularia inflata |
| title_fullStr |
A new rearranged dolabellane diterpene from the soft coral Clavularia inflata |
| title_full_unstemmed |
A new rearranged dolabellane diterpene from the soft coral Clavularia inflata |
| title_sort |
new rearranged dolabellane diterpene from the soft coral clavularia inflata |
| publisher |
Animo Repository |
| publishDate |
2008 |
| url |
https://animorepository.dlsu.edu.ph/faculty_research/1146 https://animorepository.dlsu.edu.ph/context/faculty_research/article/2145/type/native/viewcontent/14786410701640528.html |
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