Diastereoselective addition of 2-trimethylsilyloxyfuran to (S)-(+)-2-(p-tolylsulfinyl)-1,4-benzoquinone

Brimble, Margaret; Duncalf, LJ; Reid, DCW

dc.contributor.author	Brimble, Margaret	en
dc.contributor.author	Duncalf, LJ	en
dc.contributor.author	Reid, DCW	en
dc.date.accessioned	2011-09-19T01:45:27Z	en
dc.date.issued	1995	en
dc.identifier.citation	TETRAHEDRON-ASYMMETR 6(1):263-269 Jan 1995	en
dc.identifier.issn	0957-4166	en
dc.identifier.uri	http://hdl.handle.net/2292/8066	en
dc.description.abstract	The uncatalyzed addition of 2-trimethylsilyloxyfuran to (S)-(+)-2-(p-tolylsulfinyl)-1,4-benzoquinone 1 afforded a 3.4:1 ratio of the diastereomeric adducts 2:3. Acetonitrile was found to be the optimum solvent whilst the use of Lewis acid catalysts afforded lower overall yields.	en
dc.language	EN	en
dc.publisher	PERGAMON-ELSEVIER SCIENCE LTD	en
dc.relation.ispartofseries	Tetrahedron Asymmetry	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/0957-4166/	en
dc.rights.uri	https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm	en
dc.subject	DIELS-ALDER REACTIONS	en
dc.subject	CONJUGATE ADDITION	en
dc.subject	ACTIVATED QUINONES	en
dc.subject	REARRANGEMENT	en
dc.subject	ANTIBIOTICS	en
dc.subject	ADDUCTS	en
dc.subject	ROUTE	en
dc.title	Diastereoselective addition of 2-trimethylsilyloxyfuran to (S)-(+)-2-(p-tolylsulfinyl)-1,4-benzoquinone	en
dc.type	Journal Article	en
dc.identifier.doi	10.1016/0957-4166(94)00383-M	en
pubs.issue	1	en
pubs.begin-page	263	en
pubs.volume	6	en
dc.rights.holder	Copyright: 1994 Elsevier Ltd.	en
pubs.end-page	269	en
dc.rights.accessrights	http://purl.org/eprint/accessRights/RestrictedAccess	en
pubs.subtype	Article	en
pubs.elements-id	132885	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	2011-10-06	en