endo-(1'R,2'R,5'S,7'R,9'S)-2-(9'-Benzyl­oxy-2'-phenyl-3',6'-dioxabi­cyclo­[3.2.2]­nonan-7'-yl)-7-bromo-5,8-di­methoxy­naph­thalen-1-yl acetate

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dc.contributor.author Brenstrum, Timothy en
dc.contributor.author Brimble, MA en
dc.contributor.author Turner, P en
dc.date.accessioned 2011-09-19T21:12:56Z en
dc.date.issued 2001 en
dc.identifier.citation Acta Crystallographica Section E E57: O28-O29 2001 en
dc.identifier.issn 1600-5368 en
dc.identifier.uri http://hdl.handle.net/2292/8127 en
dc.description.abstract The title compound, (1), is the product of a model synthesis of an analogue of the antibiotic medermycin, and is thought to be the result of an unusual 1,6-hydride shift. en
dc.language EN en
dc.relation.ispartofseries Acta Crystallographica Section E 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/1600-5368/ en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.rights.uri http://journals.iucr.org/services/copyrightpolicy.html en
dc.subject REFINEMENT en
dc.title endo-(1'R,2'R,5'S,7'R,9'S)-2-(9'-Benzyl­oxy-2'-phenyl-3',6'-dioxabi­cyclo­[3.2.2]­nonan-7'-yl)-7-bromo-5,8-di­methoxy­naph­thalen-1-yl acetate en
dc.type Journal Article en
dc.identifier.doi 10.1107/S1600536800018092 en
pubs.begin-page O28 en
pubs.volume E57 en
dc.rights.holder Copyright: 2001 International Union of Crystallography en
pubs.end-page O29 en
dc.rights.accessrights http://purl.org/eprint/accessRights/OpenAccess en
pubs.subtype Article en
pubs.elements-id 106219 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 2010-09-01 en

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