A concise synthesis of (±) and a total synthesis of (+)-epiquinamide

Tong, Sok; Barker, David

dc.contributor.author	Tong, Sok	en
dc.contributor.author	Barker, David	en
dc.date.accessioned	2012-02-27T20:02:30Z	en
dc.date.issued	2006	en
dc.identifier.citation	Tetrahedron Letters 47(29):5017-5020 17 Jul 2006	en
dc.identifier.issn	0040-4039	en
dc.identifier.uri	http://hdl.handle.net/2292/12137	en
dc.description.abstract	A total synthesis of the quinolizidine alkaloid (+)-epiquinamide 1 has been achieved starting from ()-pipecolinic acid 3. The key step is the highly diastereoselective addition of a TBDMS-protected propargyl alcohol to a chiral aldehyde derived from 3 to give erythro alkynol 19, which is then easily transformed into the desired bicyclic skeleton.	en
dc.description.uri	http://dx.doi.org/10.1016/j.tetlet.2006.05.092	en
dc.publisher	Elsevier Ltd.	en
dc.relation.ispartofseries	Tetrahedron Letters	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/0040-4039/	en
dc.rights.uri	https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm	en
dc.title	A concise synthesis of (±) and a total synthesis of (+)-epiquinamide	en
dc.type	Journal Article	en
dc.identifier.doi	10.1016/j.tetlet.2006.05.092	en
pubs.issue	29	en
pubs.begin-page	5017	en
pubs.volume	47	en
dc.rights.holder	Copyright: Elsevier Ltd.	en
pubs.end-page	5020	en
dc.rights.accessrights	http://purl.org/eprint/accessRights/RestrictedAccess	en
pubs.subtype	Article	en
pubs.elements-id	65814	en
pubs.org-id	Science	en
pubs.org-id	Chemistry	en
pubs.record-created-at-source-date	2010-09-01	en