Diels-Alder addition of acyclic dienes to chiral naphthoquinones

Brimble, MA; Elliott, RJ; McEwan, JF

dc.contributor.author	Brimble, MA	en
dc.contributor.author	Elliott, RJ	en
dc.contributor.author	McEwan, JF	en
dc.date.accessioned	2011-09-19T01:53:52Z	en
dc.date.issued	2000	en
dc.identifier.citation	Australian Journal of Chemistry 53 (7), 571-576, 2000	en
dc.identifier.issn	0004-9425	en
dc.identifier.uri	http://hdl.handle.net/2292/8073	en
dc.description.abstract	The Diels Alder addition of naphthoquinone (2a) to 1-trimethylsilyloxybuta-1,3-diene (3) afforded a 1.4 : 1 ratio of Diels Alder adducts (5a) and (6a) which were easily separated by flash chromatography. Individual treatment of adducts (5a) and (6a)	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	Diels-Alder addition	en
dc.subject	acyclic dienes	en
dc.subject	naphthoquinone	en
dc.subject	ANNULATION	en
dc.subject	QUINONES	en
dc.title	Diels-Alder addition of acyclic dienes to chiral naphthoquinones	en
dc.type	Journal Article	en
dc.identifier.doi	10.1071/CH00074	en
pubs.issue	7	en
pubs.begin-page	571	en
pubs.volume	53	en
dc.rights.holder	Copyright: 2000 CSIRO	en
pubs.end-page	576	en
dc.rights.accessrights	http://purl.org/eprint/accessRights/RestrictedAccess	en
pubs.subtype	Article	en
pubs.elements-id	3055	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