| dc.contributor.author |
Ciminiello, P |
en |
| dc.contributor.author |
Dell'Aversano, C |
en |
| dc.contributor.author |
Fattorusso, E |
en |
| dc.contributor.author |
Forino, M |
en |
| dc.contributor.author |
Magno, S |
en |
| dc.contributor.author |
Santelia, FU |
en |
| dc.contributor.author |
Moutsos, VI |
en |
| dc.contributor.author |
Pitsinos, EN |
en |
| dc.contributor.author |
Couladouros, EA |
en |
| dc.date.accessioned |
2014-06-06T06:47:11Z |
|
| dc.date.available |
2014-06-06T06:47:11Z |
|
| dc.date.issued |
2006 |
en |
| dc.identifier.issn |
00404020 |
en |
| dc.identifier.uri |
http://dx.doi.org/10.1016/j.tet.2006.05.070 |
en |
| dc.identifier.uri |
http://62.217.125.90/xmlui/handle/123456789/3437 |
|
| dc.subject |
Adriatic shellfish |
en |
| dc.subject |
Mytilus galloprovincialis |
en |
| dc.subject |
Natural products |
en |
| dc.subject |
NMR spectroscopy |
en |
| dc.subject |
Oxazinins |
en |
| dc.subject |
Synthetic models |
en |
| dc.subject.other |
oxazinin 1 |
en |
| dc.subject.other |
oxazinin 2 |
en |
| dc.subject.other |
unclassified drug |
en |
| dc.subject.other |
article |
en |
| dc.subject.other |
diastereoisomer |
en |
| dc.subject.other |
mussel |
en |
| dc.subject.other |
nuclear magnetic resonance spectroscopy |
en |
| dc.subject.other |
priority journal |
en |
| dc.subject.other |
stereochemistry |
en |
| dc.subject.other |
structure analysis |
en |
| dc.subject.other |
toxicity |
en |
| dc.subject.other |
Mytilus galloprovincialis |
en |
| dc.title |
Oxazinins from toxic mussels: isolation of a novel oxazinin and reassignment of the C-2 configuration of oxazinin-1 and -2 on the basis of synthetic models |
en |
| heal.type |
journalArticle |
en |
| heal.identifier.primary |
10.1016/j.tet.2006.05.070 |
en |
| heal.publicationDate |
2006 |
en |
| heal.abstract |
The analysis of a batch of toxic mussels (Mytilus galloprovincialis) from the Northern Adriatic Sea led to the isolation of a novel oxazinin, oxazinin-4. Its structure including the relative stereochemistry has been elucidated through extensive NMR analysis. A synthetic route to oxazinins has been crucial in establishing the absolute stereochemistry of oxazinin-4 and for reassigning the absolute C-2 configuration of oxazinin-1 and -2 previously isolated from toxic shellfish and stereostructurally characterized. © 2006 Elsevier Ltd. All rights reserved. |
en |
| heal.journalName |
Tetrahedron |
en |
| dc.identifier.issue |
33 |
en |
| dc.identifier.volume |
62 |
en |
| dc.identifier.doi |
10.1016/j.tet.2006.05.070 |
en |
| dc.identifier.spage |
7738 |
en |
| dc.identifier.epage |
7743 |
en |