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Article: Stereoselective synthesis of functionalized pyrrolidines by ruthenium porphyrin-catalyzed decomposition of α-diazo esters and cascade azomethine ylide formation/1,3-dipolar cycloaddition reactions

TitleStereoselective synthesis of functionalized pyrrolidines by ruthenium porphyrin-catalyzed decomposition of α-diazo esters and cascade azomethine ylide formation/1,3-dipolar cycloaddition reactions
Authors
Li, GYChen, JYu, WYHong, WChe, CM
Issue Date2003
PublisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.html
Citation
Organic Letters, 2003, v. 5 n. 12, p. 2153-2156 How to Cite?
DOI: http://dx.doi.org/10.1021/ol034614v
Abstract(Matrix presented) Ruthenium porphyrins catalyze three-component coupling reaction of α-diazo esters with a series of N-benzylidene imines and alkenes to form functionalized pyrrolidines in excellent diastereoselectivities. The reaction proceeds via a reactive ruthenium-carbene intermediate and its subsequent reaction with imine to generate azomethine ylide, which reacts with alkenes via 1,3-diploar cycloaddition.
Persistent Identifierhttp://hdl.handle.net/10722/167831
ISSN
1523-7060
2021 Impact Factor: 6.072
2020 SCImago Journal Rankings: 1.940
ISI Accession Number ID
WOS:000183364200036
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorLi, GYen_US
dc.contributor.authorChen, Jen_US
dc.contributor.authorYu, WYen_US
dc.contributor.authorHong, Wen_US
dc.contributor.authorChe, CMen_US
dc.date.accessioned2012-10-08T03:12:02Z-
dc.date.available2012-10-08T03:12:02Z-
dc.date.issued2003en_US
dc.identifier.citationOrganic Letters, 2003, v. 5 n. 12, p. 2153-2156en_US
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://hdl.handle.net/10722/167831-
dc.description.abstract(Matrix presented) Ruthenium porphyrins catalyze three-component coupling reaction of α-diazo esters with a series of N-benzylidene imines and alkenes to form functionalized pyrrolidines in excellent diastereoselectivities. The reaction proceeds via a reactive ruthenium-carbene intermediate and its subsequent reaction with imine to generate azomethine ylide, which reacts with alkenes via 1,3-diploar cycloaddition.en_US
dc.languageengen_US
dc.publisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.htmlen_US
dc.relation.ispartofOrganic Lettersen_US
dc.titleStereoselective synthesis of functionalized pyrrolidines by ruthenium porphyrin-catalyzed decomposition of α-diazo esters and cascade azomethine ylide formation/1,3-dipolar cycloaddition reactionsen_US
dc.typeArticleen_US
dc.identifier.emailChe, CM:cmche@hku.hken_US
dc.identifier.authorityChe, CM=rp00670en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1021/ol034614ven_US
dc.identifier.pmid12790552-
dc.identifier.scopuseid_2-s2.0-0141519434en_US
dc.identifier.hkuros83830-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0141519434&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume5en_US
dc.identifier.issue12en_US
dc.identifier.spage2153en_US
dc.identifier.epage2156en_US
dc.identifier.isiWOS:000183364200036-
dc.publisher.placeUnited Statesen_US
dc.identifier.scopusauthoridLi, GY=15765581300en_US
dc.identifier.scopusauthoridChen, J=36047378100en_US
dc.identifier.scopusauthoridYu, WY=7403913673en_US
dc.identifier.scopusauthoridHong, W=37022928600en_US
dc.identifier.scopusauthoridChe, CM=7102442791en_US
dc.identifier.issnl1523-7052-

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