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Article: Desymmetrization of meso [3.2.1]oxabicyclic systems using metal-catalysed asymmetric intramolecular C-H insertion

TitleDesymmetrization of meso [3.2.1]oxabicyclic systems using metal-catalysed asymmetric intramolecular C-H insertion
Authors
KeywordsCopper
Meso 8 oxabicyclo( 3.2.1 )octen 3 one
Catalyst
Controlled study
Cross linking
Issue Date2011
PublisherPergamon. The Journal's web site is located at http://www.elsevier.com/locate/tetlet
Citation
Tetrahedron Letters, 2011, v. 52 n. 50, p. 6763-6766 How to Cite?
AbstractDiazoketone derivatives of meso 8-oxabicyclo[3.2.1]octen-3-ones were desymmetrized by an intramolecular C-H insertion mediated by chiral copper and dirhodium catalysts to generate oxatricyclic systems with up to 5 contiguous stereogenic centres and 50% ee.
Persistent Identifierhttp://hdl.handle.net/10722/168583
ISSN
2015 Impact Factor: 2.347
2015 SCImago Journal Rankings: 0.782
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorZhang, Xen_US
dc.contributor.authorLi, Zen_US
dc.contributor.authorChu, JCKen_US
dc.contributor.authorChiu, Pen_US
dc.date.accessioned2012-10-08T03:21:05Z-
dc.date.available2012-10-08T03:21:05Z-
dc.date.issued2011en_US
dc.identifier.citationTetrahedron Letters, 2011, v. 52 n. 50, p. 6763-6766en_US
dc.identifier.issn0040-4039en_US
dc.identifier.urihttp://hdl.handle.net/10722/168583-
dc.description.abstractDiazoketone derivatives of meso 8-oxabicyclo[3.2.1]octen-3-ones were desymmetrized by an intramolecular C-H insertion mediated by chiral copper and dirhodium catalysts to generate oxatricyclic systems with up to 5 contiguous stereogenic centres and 50% ee.en_US
dc.languageengen_US
dc.publisherPergamon. The Journal's web site is located at http://www.elsevier.com/locate/tetleten_US
dc.relation.ispartofTetrahedron Lettersen_US
dc.subjectCopperen_US
dc.subjectMeso 8 oxabicyclo( 3.2.1 )octen 3 oneen_US
dc.subjectCatalysten_US
dc.subjectControlled studyen_US
dc.subjectCross linkingen_US
dc.titleDesymmetrization of meso [3.2.1]oxabicyclic systems using metal-catalysed asymmetric intramolecular C-H insertionen_US
dc.typeArticleen_US
dc.identifier.emailChu, JCK: chujohn2@hku.hken_US
dc.identifier.emailChiu, P: pchiu@hku.hk-
dc.identifier.authorityChiu, P=rp00680en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1016/j.tetlet.2011.10.026en_US
dc.identifier.scopuseid_2-s2.0-80755175788en_US
dc.identifier.hkuros205781-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-80755175788&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume52en_US
dc.identifier.issue50en_US
dc.identifier.spage6763en_US
dc.identifier.epage6766en_US
dc.identifier.isiWOS:000297612800024-
dc.publisher.placeUnited Kingdomen_US
dc.identifier.scopusauthoridChiu, P=11140148700en_US
dc.identifier.scopusauthoridChu, JCK=35267922700en_US
dc.identifier.scopusauthoridLi, Z=54410931700en_US
dc.identifier.scopusauthoridZhang, X=54411594400en_US
dc.identifier.citeulike9930873-

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