File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Nitrido ruthenium porphyrins: Synthesis, characterization, and amination reactions with hydrocarbon or silyl enol ethers

TitleNitrido ruthenium porphyrins: Synthesis, characterization, and amination reactions with hydrocarbon or silyl enol ethers
Authors
Leung, SKYHuang, JSLiang, JLChe, CMZhou, ZY
KeywordsAmination
N ligands
Porphyrinoids
Ruthenium
Structure elucidation
Issue Date2003
PublisherWiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www3.interscience.wiley.com/journal/26737/home
Citation
Angewandte Chemie - International Edition, 2003, v. 42 n. 3, p. 340-343 How to Cite?
DOI: http://dx.doi.org/10.1002/anie.200390111
AbstractAn unprecedented synthetic strategy was used for the preparation of nitrido ruthenium(VI) porphyrins such as 1. The structure of 1 features a Ru-N (nitrido) distance of 1.656(5) Å. Reactions of nitrido ruthenium(VI) porphyrins with silyl enol ethers or indan, in the presence of trifluoroacetic anhydride, afforded N-trifluoroacetyl amines in up to 84% yield.
Persistent Identifierhttp://hdl.handle.net/10722/70410
ISSN
1433-7851
2023 Impact Factor: 16.1
2023 SCImago Journal Rankings: 5.300
ISI Accession Number ID
WOS:000180578000015
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorLeung, SKYen_HK
dc.contributor.authorHuang, JSen_HK
dc.contributor.authorLiang, JLen_HK
dc.contributor.authorChe, CMen_HK
dc.contributor.authorZhou, ZYen_HK
dc.date.accessioned2010-09-06T06:22:37Z-
dc.date.available2010-09-06T06:22:37Z-
dc.date.issued2003en_HK
dc.identifier.citationAngewandte Chemie - International Edition, 2003, v. 42 n. 3, p. 340-343en_HK
dc.identifier.issn1433-7851en_HK
dc.identifier.urihttp://hdl.handle.net/10722/70410-
dc.description.abstractAn unprecedented synthetic strategy was used for the preparation of nitrido ruthenium(VI) porphyrins such as 1. The structure of 1 features a Ru-N (nitrido) distance of 1.656(5) Å. Reactions of nitrido ruthenium(VI) porphyrins with silyl enol ethers or indan, in the presence of trifluoroacetic anhydride, afforded N-trifluoroacetyl amines in up to 84% yield.en_HK
dc.languageengen_HK
dc.publisherWiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www3.interscience.wiley.com/journal/26737/homeen_HK
dc.relation.ispartofAngewandte Chemie - International Editionen_HK
dc.subjectAminationen_HK
dc.subjectN ligandsen_HK
dc.subjectPorphyrinoidsen_HK
dc.subjectRutheniumen_HK
dc.subjectStructure elucidationen_HK
dc.titleNitrido ruthenium porphyrins: Synthesis, characterization, and amination reactions with hydrocarbon or silyl enol ethersen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1433-7851&volume=42&issue=3&spage=340&epage=343&date=2003&atitle=Nitrido+ruthenium+porphyrins:++Synthesis,+characterization,+and+amination+reactions+with+hydrocarbon+or+silyl+enol+ethersen_HK
dc.identifier.emailHuang, JS:jshuang@hkucc.hku.hken_HK
dc.identifier.emailChe, CM:cmche@hku.hken_HK
dc.identifier.authorityHuang, JS=rp00709en_HK
dc.identifier.authorityChe, CM=rp00670en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/anie.200390111en_HK
dc.identifier.scopuseid_2-s2.0-0037455261en_HK
dc.identifier.hkuros81085en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-0037455261&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume42en_HK
dc.identifier.issue3en_HK
dc.identifier.spage340en_HK
dc.identifier.epage343en_HK
dc.identifier.isiWOS:000180578000015-
dc.publisher.placeGermanyen_HK
dc.identifier.scopusauthoridLeung, SKY=36546285500en_HK
dc.identifier.scopusauthoridHuang, JS=7407192639en_HK
dc.identifier.scopusauthoridLiang, JL=7404541484en_HK
dc.identifier.scopusauthoridChe, CM=7102442791en_HK
dc.identifier.scopusauthoridZhou, ZY=7406096262en_HK
dc.identifier.issnl1433-7851-

Export via OAI-PMH Interface in XML Formats

OR

Export to Other Non-XML Formats