Structure and absolute stereochemistry of novel C-15-halogenated acetogenins from the anaspidean mollusc Aplysia dactylomela
Manzo, E; Ciavatta, ML; Gavagnin, M; Puliti, R; Mollo, E; Guo, YW; Mattia, CA; Mazzarella, L; Cimino, G
刊名TETRAHEDRON
2005-08-01
卷号61期号:31页码:7456-7460
关键词marine natural products molluscs acetogenins absolute stereochemistry
ISSN号0040-4020
DOI10.1016/j.tet.2005.05.051
文献子类Article
英文摘要Three novel halogenated C-15-acetogenins, compounds 1-3, have been isolated, together with known metabolites, from a South China Sea collection of the anaspidean mollusc Aplysia dactylomela. The structures have been suggested by both NMR analysis and comparison with literature data. The structure of 1 was confirmed by a single crystal X-ray study, which also allowed the establishment of its absolute stereochemistry. (c) 2005 Elsevier Ltd. All rights reserved.
WOS关键词SEA HARE ; LAURENCIA-PINNATIFIDA ; C-15 ACETOGENINS ; CONFIGURATION ; DITERPENE ; KURODAI ; METABOLITES ; OBTUSA
WOS研究方向Chemistry
语种英语
出版者PERGAMON-ELSEVIER SCIENCE LTD
WOS记录号WOS:000230581400013
内容类型期刊论文
源URL[http://119.78.100.183/handle/2S10ELR8/273830]  
专题新药研究国家重点实验室
中科院受体结构与功能重点实验室
通讯作者Manzo, E
作者单位1.Chinese Acad Sci, Inst Mat Med, State Key Lab Drug Res, Shanghai Inst Biol Sci, Shanghai 201203, Peoples R China
2.CNR, Ist Chim Biomol, I-80078 Pozzuoli, Na, Italy
3.Univ Naples Federico II, Dipartimento Chim, I-80126 Naples, Italy
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GB/T 7714
Manzo, E,Ciavatta, ML,Gavagnin, M,et al. Structure and absolute stereochemistry of novel C-15-halogenated acetogenins from the anaspidean mollusc Aplysia dactylomela[J]. TETRAHEDRON,2005,61(31):7456-7460.
APA Manzo, E.,Ciavatta, ML.,Gavagnin, M.,Puliti, R.,Mollo, E.,...&Cimino, G.(2005).Structure and absolute stereochemistry of novel C-15-halogenated acetogenins from the anaspidean mollusc Aplysia dactylomela.TETRAHEDRON,61(31),7456-7460.
MLA Manzo, E,et al."Structure and absolute stereochemistry of novel C-15-halogenated acetogenins from the anaspidean mollusc Aplysia dactylomela".TETRAHEDRON 61.31(2005):7456-7460.
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