Synthesis of the Bis-Spiroacetal Moiety of 17-epi-20-Deoxysalinomycin

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dc.contributor.author Brimble, Margaret en
dc.contributor.author Williams, GM en
dc.date.accessioned 2011-09-21T22:32:34Z en
dc.date.issued 1992 en
dc.identifier.citation Journal of Organic Chemistry 57(22):5818-5822 1992 en
dc.identifier.issn 0022-3263 en
dc.identifier.uri http://hdl.handle.net/2292/8217 en
dc.description.abstract The synthesis of the bis-spiroacetal moiety of 17-epi-20-deoxysalinomycin (4) is reported in which the key step involves oxidative cyclization of the hydroxy spiroacetals 14 and 15 to the bis-spiroacetals 16 and 17 using (diacetoxyiodo)benzene and iodine under photolytic conditions. en
dc.relation.ispartofseries Journal of Organic Chemistry 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/0022-3263/ en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.title Synthesis of the Bis-Spiroacetal Moiety of 17-epi-20-Deoxysalinomycin en
dc.type Journal Article en
dc.identifier.doi 10.1021/jo00048a009 en
pubs.issue 22 en
pubs.begin-page 5818 en
pubs.volume 57 en
dc.rights.holder Copyright: 1992 American Chemical Society en
pubs.end-page 5822 en
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.subtype Article en
pubs.elements-id 154181 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 2010-09-29 en


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