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Article: Asymmetric synthesis of multifunctionalized pyrrolines by a ruthenium porphyrin-catalyzed three-component coupling reaction

TitleAsymmetric synthesis of multifunctionalized pyrrolines by a ruthenium porphyrin-catalyzed three-component coupling reaction
Authors
Xu, HWLi, GYWong, MKChe, CM
Issue Date2005
PublisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.html
Citation
Organic Letters, 2005, v. 7 n. 24, p. 5349-5352 How to Cite?
DOI: http://dx.doi.org/10.1021/ol050819n
Abstract(Chemical Equation Presented) Chiral multifunctionalized pyrrolines have been synthesized by a ruthenium porphyrin catalyzed three-component coupling reaction. In a one-pot reaction, ruthenium porphyrins catalyzed in situ generation of chiral azomethine ylides from chiral diazo esters and imines. Asymmetric 1,3-dipolar cycloaddition reactions of the chiral azomethine ylides with dipolarophiles afforded the corresponding pyrrolines in good yields and high diastereoselectivity (up to 92% de). © 2005 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/69787
ISSN
1523-7060
2023 Impact Factor: 4.9
2023 SCImago Journal Rankings: 1.245
ISI Accession Number ID
WOS:000233505700001
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorXu, HWen_HK
dc.contributor.authorLi, GYen_HK
dc.contributor.authorWong, MKen_HK
dc.contributor.authorChe, CMen_HK
dc.date.accessioned2010-09-06T06:16:50Z-
dc.date.available2010-09-06T06:16:50Z-
dc.date.issued2005en_HK
dc.identifier.citationOrganic Letters, 2005, v. 7 n. 24, p. 5349-5352en_HK
dc.identifier.issn1523-7060en_HK
dc.identifier.urihttp://hdl.handle.net/10722/69787-
dc.description.abstract(Chemical Equation Presented) Chiral multifunctionalized pyrrolines have been synthesized by a ruthenium porphyrin catalyzed three-component coupling reaction. In a one-pot reaction, ruthenium porphyrins catalyzed in situ generation of chiral azomethine ylides from chiral diazo esters and imines. Asymmetric 1,3-dipolar cycloaddition reactions of the chiral azomethine ylides with dipolarophiles afforded the corresponding pyrrolines in good yields and high diastereoselectivity (up to 92% de). © 2005 American Chemical Society.en_HK
dc.languageengen_HK
dc.publisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.htmlen_HK
dc.relation.ispartofOrganic Lettersen_HK
dc.titleAsymmetric synthesis of multifunctionalized pyrrolines by a ruthenium porphyrin-catalyzed three-component coupling reactionen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1523-7060&volume=7&spage=5349&epage=5352&date=2005&atitle=Asymmetric+synthesis+of+multifunctionalized+pyrrolines+by+a+ruthenium+porphyrin-catalyzed+three-component+coupling+reaction+en_HK
dc.identifier.emailChe, CM:cmche@hku.hken_HK
dc.identifier.authorityChe, CM=rp00670en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/ol050819nen_HK
dc.identifier.scopuseid_2-s2.0-28844498979en_HK
dc.identifier.hkuros118004en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-28844498979&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume7en_HK
dc.identifier.issue24en_HK
dc.identifier.spage5349en_HK
dc.identifier.epage5352en_HK
dc.identifier.isiWOS:000233505700001-
dc.publisher.placeUnited Statesen_HK
dc.identifier.scopusauthoridXu, HW=7407450997en_HK
dc.identifier.scopusauthoridLi, GY=15765581300en_HK
dc.identifier.scopusauthoridWong, MK=7403908449en_HK
dc.identifier.scopusauthoridChe, CM=7102442791en_HK
dc.identifier.issnl1523-7052-

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