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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Bibliographic Details
Main Authors: Alea, Glenn V., Bowden, Bruce F., Ragasa, Consolacion Y.
Format: text
Published: Animo Repository 2008
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Online Access: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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Institution: De La Salle University
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Summary: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.