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
2011 Impact Factor: 6.169
2011 SCImago Journal Rankings: 0.507
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 Field
Value
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
2011 Impact Factor: 6.169
2011 SCImago Journal Rankings: 0.507
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
Author Affiliations
  1. Institute of Molecular Technology for Drug Discovery and Synthesis, Hong Kong