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- Publisher Website: 10.1002/anie.200902471
- Scopus: eid_2-s2.0-70349922826
- PMID: 19718730
- WOS: WOS:000269979100021
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Article: Acid-catalyzed intramolecular [2+2] Cycloaddition of ene-allenones: Facile access to bicyclo[n.2.0] frameworks
Title | Acid-catalyzed intramolecular [2+2] Cycloaddition of ene-allenones: Facile access to bicyclo[n.2.0] frameworks |
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Authors | |
Keywords | Acid catalysis Cycloaddition Cyclobutanes Multiple bonds Used-ring systems |
Issue Date | 2009 |
Publisher | Wiley - 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? |
Abstract | Two 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 Identifier | http://hdl.handle.net/10722/182336 |
ISSN | 2023 Impact Factor: 16.1 2023 SCImago Journal Rankings: 5.300 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Zhao, JF | en_US |
dc.contributor.author | Loh, TP | en_US |
dc.date.accessioned | 2013-04-23T08:18:59Z | - |
dc.date.available | 2013-04-23T08:18:59Z | - |
dc.date.issued | 2009 | en_US |
dc.identifier.citation | Angewandte Chemie - International Edition, 2009, v. 48 n. 39, p. 7232-7235 | en_US |
dc.identifier.issn | 1433-7851 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/182336 | - |
dc.description.abstract | Two 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.language | eng | en_US |
dc.publisher | Wiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www3.interscience.wiley.com/journal/26737/home | en_US |
dc.relation.ispartof | Angewandte Chemie - International Edition | en_US |
dc.subject | Acid catalysis | - |
dc.subject | Cycloaddition | - |
dc.subject | Cyclobutanes | - |
dc.subject | Multiple bonds | - |
dc.subject | Used-ring systems | - |
dc.subject.mesh | Alkenes - Chemistry | en_US |
dc.subject.mesh | Bicyclo Compounds - Chemistry | en_US |
dc.subject.mesh | Catalysis | en_US |
dc.subject.mesh | Cyclization | en_US |
dc.subject.mesh | Molecular Structure | en_US |
dc.title | Acid-catalyzed intramolecular [2+2] Cycloaddition of ene-allenones: Facile access to bicyclo[n.2.0] frameworks | en_US |
dc.type | Article | en_US |
dc.identifier.email | Zhao, JF: zhao0065@e.ntu.edu.sg | en_US |
dc.identifier.authority | Zhao, JF=rp01745 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1002/anie.200902471 | en_US |
dc.identifier.pmid | 19718730 | - |
dc.identifier.scopus | eid_2-s2.0-70349922826 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-70349922826&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 48 | en_US |
dc.identifier.issue | 39 | en_US |
dc.identifier.spage | 7232 | en_US |
dc.identifier.epage | 7235 | en_US |
dc.identifier.isi | WOS:000269979100021 | - |
dc.publisher.place | Germany | en_US |
dc.identifier.scopusauthorid | Zhao, JF=8393022100 | en_US |
dc.identifier.scopusauthorid | Loh, TP=35234192600 | en_US |
dc.identifier.issnl | 1433-7851 | - |