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Verticillane and Norverticillane Diterpenoids from the Formosan Soft Coral Cespitularia hypotentaculata
Author(s) -
Chang JiunYang,
Abd ElRazek Mohamed H.,
Shen YaChing
Publication year - 2009
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.200900224
Subject(s) - chemistry , coral , skeleton (computer programming) , lactone , stereochemistry , diene , organic chemistry , anatomy , natural rubber , medicine , art , visual arts
Five new diterpenes, cespihypotins W–Z ( 1 – 4 , resp.) and cespihypotone ( 5 ) have been isolated from the AcOEt‐soluble fraction of the Formosan soft coral Cespitularia hypotentaculata. Two of them having the norverticillane skeleton, i.e. , 1 and 2 , and the other three, 3 – 5 , possessing a verticillane skeleton. The structures were established as (+)‐(1 β H,7 E )‐6 β ,11 β ‐dihydroxynorverticilla‐4(18),7‐diene‐10,12‐dione ( 1 ), (+)‐(1 β H,7 E )‐6 β ‐acetoxy‐11 β ‐hydroxynorverticilla‐4(18),7‐diene‐10,12‐dione ( 2 ), (−)‐(1 β H,7 E )‐6 β ‐acetoxyverticilla‐4(18),7,11‐triene‐10,12‐ γ ‐lactone ( 3 ), (+)‐(1 β H,7 E )‐6 β ‐acetoxy‐10‐hydroxyverticilla‐4(18),7,11‐triene‐10,12‐ γ ‐lactone ( 4 ), and (+)‐(1 β H,3 Z )‐10 β ‐hydroxy‐6‐oxoverticilla‐3,11‐diene‐10,12‐ γ ‐lactone ( 5 ), respectively, on the basis of 1D‐ and 2D‐NMR spectroscopic analyses.

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