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Article: [Fe(F20TPP)Cl] catalyzed intramolecular C-N bond formation for alkaloid synthesis using aryl azides as nitrogen source

Title[Fe(F20TPP)Cl] catalyzed intramolecular C-N bond formation for alkaloid synthesis using aryl azides as nitrogen source
Authors
Liu, YWei, JChe, CM
Issue Date2010
PublisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/Publishing/Journals/cc/index.asp
Citation
Chemical Communications, 2010, v. 46 n. 37, p. 6926-6928 How to Cite?
DOI: http://dx.doi.org/10.1039/c0cc01825b
AbstractThe syntheses of alkaloids including indoles, indolines, tetrahydroquinolines, dihydroquinazolinones and quinazolinones have been accomplished in moderate to excellent yields via [Fe(F20TPP)Cl] catalyzed intramolecular C-N bond formation using aryl azides as nitrogen source. © 2010 The Royal Society of Chemistry.
Persistent Identifierhttp://hdl.handle.net/10722/134360
ISSN
1359-7345
2023 Impact Factor: 4.3
2023 SCImago Journal Rankings: 1.133
ISI Accession Number ID
WOS:000282476600012
Funding AgencyGrant Number
Hong Kong Research Grants CouncilHKU 7007/08
HKU/CRF/01/08
University Grants Committee of the Hong Kong Special Administrative Region, ChinaAoE 10/01P
Funding Information:

This work was supported by the Hong Kong Research Grants Council (HKU 7007/08 and HKU/CRF/01/08), and the Areas of Excellence Scheme established under the University Grants Committee of the Hong Kong Special Administrative Region, China (AoE 10/01P).

References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorLiu, Yen_HK
dc.contributor.authorWei, Jen_HK
dc.contributor.authorChe, CMen_HK
dc.date.accessioned2011-06-17T09:18:37Z-
dc.date.available2011-06-17T09:18:37Z-
dc.date.issued2010en_HK
dc.identifier.citationChemical Communications, 2010, v. 46 n. 37, p. 6926-6928en_HK
dc.identifier.issn1359-7345en_HK
dc.identifier.urihttp://hdl.handle.net/10722/134360-
dc.description.abstractThe syntheses of alkaloids including indoles, indolines, tetrahydroquinolines, dihydroquinazolinones and quinazolinones have been accomplished in moderate to excellent yields via [Fe(F20TPP)Cl] catalyzed intramolecular C-N bond formation using aryl azides as nitrogen source. © 2010 The Royal Society of Chemistry.en_HK
dc.languageengen_US
dc.publisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/Publishing/Journals/cc/index.aspen_HK
dc.relation.ispartofChemical Communicationsen_HK
dc.subject.meshAlkaloids - chemical synthesis - chemistry-
dc.subject.meshAzides - chemistry-
dc.subject.meshCatalysis-
dc.subject.meshCyclization-
dc.subject.meshIron Compounds - chemistry-
dc.title[Fe(F20TPP)Cl] catalyzed intramolecular C-N bond formation for alkaloid synthesis using aryl azides as nitrogen sourceen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1359-7345&volume=46&issue=37&spage=6926&epage=6928&date=2010&atitle=[Fe(F(20)TPP)Cl]+catalyzed+intramolecular+C-N+bond+formation+for+alkaloid+synthesis+using+aryl+azides+as+nitrogen+source-
dc.identifier.emailLiu, Y:lyg100@hku.hken_HK
dc.identifier.emailChe, CM:cmche@hku.hken_HK
dc.identifier.authorityLiu, Y=rp00749en_HK
dc.identifier.authorityChe, CM=rp00670en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/c0cc01825ben_HK
dc.identifier.pmid20730175-
dc.identifier.scopuseid_2-s2.0-77956473043en_HK
dc.identifier.hkuros185671en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-77956473043&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume46en_HK
dc.identifier.issue37en_HK
dc.identifier.spage6926en_HK
dc.identifier.epage6928en_HK
dc.identifier.isiWOS:000282476600012-
dc.publisher.placeUnited Kingdomen_HK
dc.identifier.scopusauthoridLiu, Y=8225912600en_HK
dc.identifier.scopusauthoridWei, J=37027563700en_HK
dc.identifier.scopusauthoridChe, CM=7102442791en_HK
dc.identifier.issnl1359-7345-

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