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Article: Acid-catalyzed intramolecular [2+2] Cycloaddition of ene-allenones: Facile access to bicyclo[n.2.0] frameworks

TitleAcid-catalyzed intramolecular [2+2] Cycloaddition of ene-allenones: Facile access to bicyclo[n.2.0] frameworks
Authors
Issue Date2009
PublisherWiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www3.interscience.wiley.com/journal/26737/home
Citation
Angewandte Chemie - International Edition, 2009, v. 48 n. 39, p. 7232-7235 How to Cite?
AbstractTwo plus two equals a bicycle: A highly efficient acidcatalyzed intramolecular [2+2] cycloaddition of eneallenones affords strained bicyclo[n.2.0] frameworks, which contain vicinal all-carbon quaternary and tertiary centers (see scheme; Tf: trifluoromethanesulfonyl), under mild conditions with excellent yields and chemo-, regio-, and diastereoselectivities. © 2009 Wiley-VCH Verlag GmbH & Co. KCaA.
Persistent Identifierhttp://hdl.handle.net/10722/182336
ISSN
2015 Impact Factor: 11.709
2015 SCImago Journal Rankings: 6.229
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorZhao, JFen_US
dc.contributor.authorLoh, TPen_US
dc.date.accessioned2013-04-23T08:18:59Z-
dc.date.available2013-04-23T08:18:59Z-
dc.date.issued2009en_US
dc.identifier.citationAngewandte Chemie - International Edition, 2009, v. 48 n. 39, p. 7232-7235en_US
dc.identifier.issn1433-7851en_US
dc.identifier.urihttp://hdl.handle.net/10722/182336-
dc.description.abstractTwo plus two equals a bicycle: A highly efficient acidcatalyzed intramolecular [2+2] cycloaddition of eneallenones affords strained bicyclo[n.2.0] frameworks, which contain vicinal all-carbon quaternary and tertiary centers (see scheme; Tf: trifluoromethanesulfonyl), under mild conditions with excellent yields and chemo-, regio-, and diastereoselectivities. © 2009 Wiley-VCH Verlag GmbH & Co. KCaA.en_US
dc.languageengen_US
dc.publisherWiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www3.interscience.wiley.com/journal/26737/homeen_US
dc.relation.ispartofAngewandte Chemie - International Editionen_US
dc.subject.meshAlkenes - Chemistryen_US
dc.subject.meshBicyclo Compounds - Chemistryen_US
dc.subject.meshCatalysisen_US
dc.subject.meshCyclizationen_US
dc.subject.meshMolecular Structureen_US
dc.titleAcid-catalyzed intramolecular [2+2] Cycloaddition of ene-allenones: Facile access to bicyclo[n.2.0] frameworksen_US
dc.typeArticleen_US
dc.identifier.emailZhao, JF: zhao0065@e.ntu.edu.sgen_US
dc.identifier.authorityZhao, JF=rp01745en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1002/anie.200902471en_US
dc.identifier.pmid19718730-
dc.identifier.scopuseid_2-s2.0-70349922826en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-70349922826&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume48en_US
dc.identifier.issue39en_US
dc.identifier.spage7232en_US
dc.identifier.epage7235en_US
dc.identifier.isiWOS:000269979100021-
dc.publisher.placeGermanyen_US
dc.identifier.scopusauthoridZhao, JF=8393022100en_US
dc.identifier.scopusauthoridLoh, TP=35234192600en_US

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