Synthesis of an oxaspirolactone intermediate for the synthesis of spirolides

Brimble, MA; Fares, FA; Turner, P

dc.contributor.author	Brimble, MA	en
dc.contributor.author	Fares, FA	en
dc.contributor.author	Turner, P	en
dc.date.accessioned	2011-09-19T22:06:30Z	en
dc.date.issued	2000	en
dc.identifier.citation	AUST J CHEM 53(10):845-851 2000	en
dc.identifier.issn	0004-9425	en
dc.identifier.uri	http://hdl.handle.net/2292/8164	en
dc.description.abstract	A new method has been established for the preparation of C 2-oxidized 5,5-spiroacetals, which are key intermediates for the synthesis of the bis-spiroacetal moiety of the spirolides. A bridged orthoester was used as a masked carboxylic acid in the pr	en
dc.language	EN	en
dc.relation.ispartofseries	Australian Journal of 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/0004-9425/	en
dc.rights.uri	https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm	en
dc.subject	spirolides	en
dc.subject	oxaspirolactones	en
dc.subject	spirolactones	en
dc.subject	ROUTE	en
dc.subject	CONSTRUCTION	en
dc.subject	CALCIMYCIN	en
dc.subject	SPIROKETAL	en
dc.title	Synthesis of an oxaspirolactone intermediate for the synthesis of spirolides	en
dc.type	Journal Article	en
dc.identifier.doi	10.1071/CH00111	en
pubs.issue	10	en
pubs.begin-page	845	en
pubs.volume	53	en
dc.rights.holder	Copyright: 2000 CSIRO	en
pubs.end-page	851	en
dc.rights.accessrights	http://purl.org/eprint/accessRights/RestrictedAccess	en
pubs.subtype	Article	en
pubs.elements-id	3521	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