1,4-Addition of 2-trimethylsilyloxyfuran to quinones: A facile route to the furo[3,2-b]benzofuran nucleus

Brimble, Margaret; Gibson, JJ; Baker, R; Brimble, MT; Kee, AA; O'Mahony, MJ

dc.contributor.author	Brimble, Margaret	en
dc.contributor.author	Gibson, JJ	en
dc.contributor.author	Baker, R	en
dc.contributor.author	Brimble, MT	en
dc.contributor.author	Kee, AA	en
dc.contributor.author	O'Mahony, MJ	en
dc.date.accessioned	2011-09-18T22:36:30Z	en
dc.date.issued	1987	en
dc.identifier.citation	Tetrahedron Letters 28(41):4891-4892 1987	en
dc.identifier.issn	0040-4039	en
dc.identifier.uri	http://hdl.handle.net/2292/8002	en
dc.description.abstract	The uncatalysed addition of 2-trimethylsilyloxyfuran (3) to a range of activated quinones (4) and (6) yields the crystalline adducts (5) and (7) in 51-91% yield. This novel furofuran-annulation to a quinone system provides a facile entry to the furo[3,2-b]benzofuran ring system. © 1987.	en
dc.language	EN	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	1,4-Addition of 2-trimethylsilyloxyfuran to quinones: A facile route to the furo[3,2-b]benzofuran nucleus	en
dc.type	Journal Article	en
dc.identifier.doi	10.1016/S0040-4039(00)96653-X	en
pubs.issue	41	en
pubs.begin-page	4891	en
pubs.volume	28	en
dc.rights.holder	Copyright: 1987 Elsevier Ltd.	en
pubs.end-page	4892	en
dc.rights.accessrights	http://purl.org/eprint/accessRights/RestrictedAccess	en
pubs.subtype	Article	en
pubs.elements-id	137353	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	2013-06-05	en