Total Synthesis of Paecilospirone

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dc.contributor.author Yuen, TY en
dc.contributor.author Yang, Sung Hyun en
dc.contributor.author Brimble, Margaret en
dc.date.accessioned 2011-10-25T01:56:33Z en
dc.date.issued 2011 en
dc.identifier.citation Angewandte Chemie International Edition 50(36):8350-8353 2011 en
dc.identifier.issn 1433-7851 en
dc.identifier.uri http://hdl.handle.net/2292/8433 en
dc.description.abstract In 2000, Namikoshi et al. reported the isolation and structural elucidation of a novel [5,6]-bisbenzannulated spiroacetal [1] from the marine fungus Paecilomyces sp. [2] This unique spiro[chroman-2,1’(3’H)-isobenzofuran] derivative was identified as a potential antimitotic agent (20 % inhibition at 50 mm) using an assay screening for microtubule assembly inhibitors and was subsequently named paecilospirone (1). en
dc.language ENG en
dc.publisher Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim en
dc.relation.ispartofseries Angewandte Chemie International Edition 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/1433-7851/ en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.title Total Synthesis of Paecilospirone en
dc.type Journal Article en
dc.identifier.doi 10.1002/anie.201103117 en
pubs.issue 36 en
pubs.begin-page 8350 en
pubs.volume 50 en
dc.rights.holder Copyright: Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim en
dc.identifier.pmid 21780263 en
pubs.end-page 8353 en
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.subtype Article en
pubs.elements-id 217263 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
dc.identifier.eissn 1521-3773 en
pubs.record-created-at-source-date 2011-10-21 en
pubs.dimensions-id 21780263 en


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