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

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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

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