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Article: [Fe(F20TPP)Cl] catalyzed intramolecular C-N bond formation for alkaloid synthesis using aryl azides as nitrogen source
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Title[Fe(F20TPP)Cl] catalyzed intramolecular C-N bond formation for alkaloid synthesis using aryl azides as nitrogen source
 
AuthorsLiu, Y1
Wei, J1
Che, CM1
 
Issue Date2010
 
PublisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/Publishing/Journals/cc/index.asp
 
CitationChemical 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.
 
ISSN1359-7345
2013 Impact Factor: 6.718
2013 SCImago Journal Rankings: 2.918
 
DOIhttp://dx.doi.org/10.1039/c0cc01825b
 
ISI Accession Number IDWOS: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).

 
ReferencesReferences in Scopus
 
DC FieldValue
dc.contributor.authorLiu, Y
 
dc.contributor.authorWei, J
 
dc.contributor.authorChe, CM
 
dc.date.accessioned2011-06-17T09:18:37Z
 
dc.date.available2011-06-17T09:18:37Z
 
dc.date.issued2010
 
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.
 
dc.description.naturelink_to_subscribed_fulltext
 
dc.identifier.citationChemical Communications, 2010, v. 46 n. 37, p. 6926-6928 [How to Cite?]
DOI: http://dx.doi.org/10.1039/c0cc01825b
 
dc.identifier.doihttp://dx.doi.org/10.1039/c0cc01825b
 
dc.identifier.epage6928
 
dc.identifier.hkuros185671
 
dc.identifier.isiWOS: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).

 
dc.identifier.issn1359-7345
2013 Impact Factor: 6.718
2013 SCImago Journal Rankings: 2.918
 
dc.identifier.issue37
 
dc.identifier.openurl
 
dc.identifier.pmid20730175
 
dc.identifier.scopuseid_2-s2.0-77956473043
 
dc.identifier.spage6926
 
dc.identifier.urihttp://hdl.handle.net/10722/134360
 
dc.identifier.volume46
 
dc.languageeng
 
dc.publisherRoyal Society of Chemistry. The Journal's web site is located at http://www.rsc.org/Publishing/Journals/cc/index.asp
 
dc.publisher.placeUnited Kingdom
 
dc.relation.ispartofChemical Communications
 
dc.relation.referencesReferences in Scopus
 
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 source
 
dc.typeArticle
 
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Author Affiliations
  1. Institute of Molecular Technology for Drug Discovery and Synthesis, Hong Kong