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Article: An efficient synthesis of 1,3-cyclohexadienes from oxabicyclo[2.2.1]heptenes via tandem ring opening-Peterson elimination reactions

TitleAn efficient synthesis of 1,3-cyclohexadienes from oxabicyclo[2.2.1]heptenes via tandem ring opening-Peterson elimination reactions
Authors
Issue Date1992
PublisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/joc
Citation
Journal Of Organic Chemistry, 1992, v. 57 n. 15, p. 4065-4066 How to Cite?
AbstractOxabicyclo[2.2.1]heptenes react with PhMe2SiLi or PhMe2SiCu·LiCN to yield 1,3-cyclohexadienes. The reaction pathway is shown to proceed via an addition-elimination-Peterson olefination sequence. © 1992 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/167394
ISSN
2015 Impact Factor: 4.785
2015 SCImago Journal Rankings: 2.095
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLautens, Men_US
dc.contributor.authorMa, Sen_US
dc.contributor.authorBelter, RKen_US
dc.contributor.authorChiu, Pen_US
dc.contributor.authorLeschziner, Aen_US
dc.date.accessioned2012-10-08T03:06:25Z-
dc.date.available2012-10-08T03:06:25Z-
dc.date.issued1992en_US
dc.identifier.citationJournal Of Organic Chemistry, 1992, v. 57 n. 15, p. 4065-4066en_US
dc.identifier.issn0022-3263en_US
dc.identifier.urihttp://hdl.handle.net/10722/167394-
dc.description.abstractOxabicyclo[2.2.1]heptenes react with PhMe2SiLi or PhMe2SiCu·LiCN to yield 1,3-cyclohexadienes. The reaction pathway is shown to proceed via an addition-elimination-Peterson olefination sequence. © 1992 American Chemical Society.en_US
dc.languageengen_US
dc.publisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/jocen_US
dc.relation.ispartofJournal of Organic Chemistryen_US
dc.titleAn efficient synthesis of 1,3-cyclohexadienes from oxabicyclo[2.2.1]heptenes via tandem ring opening-Peterson elimination reactionsen_US
dc.typeArticleen_US
dc.identifier.emailChiu, P:pchiu@hku.hken_US
dc.identifier.authorityChiu, P=rp00680en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1021/jo00041a003-
dc.identifier.scopuseid_2-s2.0-0009485952en_US
dc.identifier.volume57en_US
dc.identifier.issue15en_US
dc.identifier.spage4065en_US
dc.identifier.epage4066en_US
dc.identifier.isiWOS:A1992JE83500003-
dc.publisher.placeUnited Statesen_US
dc.identifier.scopusauthoridLautens, M=26643350000en_US
dc.identifier.scopusauthoridMa, S=7403725552en_US
dc.identifier.scopusauthoridBelter, RK=6602083261en_US
dc.identifier.scopusauthoridChiu, P=11140148700en_US
dc.identifier.scopusauthoridLeschziner, A=15076006900en_US

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