Synthesis of benzannulated spiroketals using an oxidative radical cyclization

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dc.contributor.author Sperry, Jonathan en
dc.contributor.author Liu, YC en
dc.contributor.author Wilson, Zoe en
dc.contributor.author Hubert, JG en
dc.contributor.author Brimble, Margaret en
dc.date.accessioned 2011-09-18T21:36:19Z en
dc.date.accessioned 2011-10-25T19:48:05Z en
dc.date.issued 2011 en
dc.identifier.citation Synthesis 2011(9):1383-1398 2011 en
dc.identifier.issn 0039-7881 en
dc.identifier.uri http://hdl.handle.net/2292/8441 en
dc.description.abstract The synthesis of both mono and bisbenzannulated spiroketals using an oxidative radical cyclization approach is investigated. Although unsuccessful in uncovering a novel route toward bisbenzannulated spiroketals, the oxidative radical cyclization does facilitate a new approach to monobenzannulated spiroketals such as those found in berkelic acid and in the chaetoquadrins. en
dc.language EN en
dc.publisher Georg Thieme Verlag Stuttgart New York en
dc.relation.ispartofseries Synthesis en
dc.relation.replaces http://hdl.handle.net/2292/7972 en
dc.relation.replaces 2292/7972 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/0039-7881/ en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.subject spiroketals en
dc.subject berkelic acid en
dc.subject chaetoquadrin en
dc.subject radical cyclization en
dc.subject cross-metathesis en
dc.subject INTRAMOLECULAR HYDROGEN ABSTRACTION en
dc.subject BERKELIC ACID en
dc.subject CROSS-METATHESIS en
dc.subject NATURAL-PRODUCTS en
dc.subject GAMMA-RUBROMYCIN en
dc.subject (-)-BERKELIC ACID en
dc.subject CONVERGENT ROUTE en
dc.subject HUMAN TELOMERASE en
dc.subject FORMAL SYNTHESIS en
dc.subject DNA HELICASE en
dc.title Synthesis of benzannulated spiroketals using an oxidative radical cyclization en
dc.type Journal Article en
dc.identifier.doi 10.1055/s-0030-1259981 en
pubs.issue 9 en
pubs.begin-page 1383 en
pubs.volume 2011 en
dc.rights.holder Copyright: Georg Thieme Verlag Stuttgart - New York en
pubs.end-page 1398 en
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.subtype Article en
pubs.elements-id 209497 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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