Synthesis of the FG ring fragment of pectenotoxins 1-9

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dc.contributor.author Heapy, Amanda en
dc.contributor.author Brimble, Margaret en
dc.date.accessioned 2011-09-18T22:35:12Z en
dc.date.issued 2010 en
dc.identifier.citation TETRAHEDRON 66(29):5424-5431 17 Jul 2010 en
dc.identifier.issn 0040-4020 en
dc.identifier.uri http://hdl.handle.net/2292/7987 en
dc.description.abstract The synthesis of the FG ring fragment common to pectenotoxins 1-9 is reported. The successful, convergent synthesis relied on high yielding routes to access two key intermediates; aldehyde 1 and phosphonium salt 2. A Z-selective Wittig reaction gave access to advanced linear precursor 3, which was converted to FG ring fragment 4 using two sequential cyclization reactions. (C) 2010 Elsevier Ltd. All rights reserved. en
dc.language EN en
dc.publisher PERGAMON-ELSEVIER SCIENCE LTD en
dc.relation.ispartofseries TETRAHEDRON en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. Details obtained from http://www.sherpa.ac.uk/romeo/issn/0040-4020/ en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.subject Pectenotoxins en
dc.subject Shellfish toxins en
dc.subject Wittig reaction en
dc.subject Sharpless asymmetric dihydroxylation en
dc.subject Horner/Wadsworth/Emmons reaction en
dc.subject STEREOCONTROLLED CYCLIZATION en
dc.subject ALKOXIDE PRECOORDINATION en
dc.subject ASYMMETRIC SYNTHESES en
dc.subject AB SPIROACETAL en
dc.subject PART II en
dc.subject COMMON en
dc.subject HYDROGENATION en
dc.subject PRECURSOR en
dc.subject SUBUNIT en
dc.subject ACCESS en
dc.title Synthesis of the FG ring fragment of pectenotoxins 1-9 en
dc.type Journal Article en
dc.identifier.doi 10.1016/j.tet.2010.05.027 en
pubs.issue 29 en
pubs.begin-page 5424 en
pubs.volume 66 en
dc.rights.holder Copyright: 2010 Elsevier Ltd en
pubs.end-page 5431 en
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.subtype Article en
pubs.elements-id 119856 en
pubs.org-id Science en
pubs.org-id Chemistry en
pubs.org-id Science Research en
pubs.org-id Maurice Wilkins Centre (2010-2014) en
pubs.record-created-at-source-date 2011-06-30 en


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