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

Brimble, Margaret; Williams, GM

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