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

Brenstrum, Timothy; Brimble, MA; Turner, P

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