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Article: Metal-catalyzed cyclopropanation on the 8-oxabicyclo[3.2.1]oct-6-ene template

TitleMetal-catalyzed cyclopropanation on the 8-oxabicyclo[3.2.1]oct-6-ene template
Authors
KeywordsChemistry
Organic chemistry
Issue Date2005
PublisherPergamon. The Journal's web site is located at http://www.elsevier.com/locate/tetlet
Citation
Tetrahedron Letters, 2005, v. 46 n. 15, p. 2709-2712 How to Cite?
AbstractCyclopropanations of an 8-oxabicyclo[3.2.1]octene substrate using diazocarbonyl compounds provided exo, exo-cyclopropanated products as the sole or major diastereomeric oxatricyclic products. Reductive cleavage of a meso-oxatricyclic ketone by samarium iodide resulted in desymmetrization without concomitant oxygen bridge cleavage. © 2005 Elsevier Ltd. All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/48525
ISSN
2015 Impact Factor: 2.347
2015 SCImago Journal Rankings: 0.782
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorLeung, SKen_HK
dc.contributor.authorChiu, Pen_HK
dc.date.accessioned2008-05-22T04:16:12Z-
dc.date.available2008-05-22T04:16:12Z-
dc.date.issued2005en_HK
dc.identifier.citationTetrahedron Letters, 2005, v. 46 n. 15, p. 2709-2712en_HK
dc.identifier.issn0040-4039en_HK
dc.identifier.urihttp://hdl.handle.net/10722/48525-
dc.description.abstractCyclopropanations of an 8-oxabicyclo[3.2.1]octene substrate using diazocarbonyl compounds provided exo, exo-cyclopropanated products as the sole or major diastereomeric oxatricyclic products. Reductive cleavage of a meso-oxatricyclic ketone by samarium iodide resulted in desymmetrization without concomitant oxygen bridge cleavage. © 2005 Elsevier Ltd. All rights reserved.en_HK
dc.format.extent136139 bytes-
dc.format.extent25778 bytes-
dc.format.mimetypeapplication/pdf-
dc.format.mimetypeapplication/pdf-
dc.languageengen_HK
dc.languagefreen_HK
dc.languagegeren_HK
dc.publisherPergamon. The Journal's web site is located at http://www.elsevier.com/locate/tetleten_HK
dc.relation.ispartofTetrahedron Lettersen_HK
dc.rightsCreative Commons: Attribution 3.0 Hong Kong License-
dc.subjectChemistryen_HK
dc.subjectOrganic chemistryen_HK
dc.titleMetal-catalyzed cyclopropanation on the 8-oxabicyclo[3.2.1]oct-6-ene templateen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0040-4039&volume=46&issue=15&spage=2709&epage=2712&date=2005&atitle=Metal-catalyzed+cyclopropanation+on+the+8-oxabicyclo[3.2.1]oct-6-ene+templateen_HK
dc.identifier.emailChiu, P:pchiu@hku.hken_HK
dc.identifier.authorityChiu, P=rp00680en_HK
dc.description.naturepostprinten_HK
dc.identifier.doi10.1016/j.tetlet.2005.01.182en_HK
dc.identifier.scopuseid_2-s2.0-15244358177en_HK
dc.identifier.hkuros98676-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-15244358177&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume46en_HK
dc.identifier.issue15en_HK
dc.identifier.spage2709en_HK
dc.identifier.epage2712en_HK
dc.identifier.isiWOS:000228115600042-
dc.publisher.placeUnited Kingdomen_HK
dc.identifier.scopusauthoridLeung, SK=7202044927en_HK
dc.identifier.scopusauthoridChiu, P=11140148700en_HK

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