Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/101625
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKumaran, Elumalaien
dc.contributor.authorHow, Kai Tong Soniaen
dc.contributor.authorGanguly, Rakeshen
dc.contributor.authorLi, Yongxinen
dc.contributor.authorLeong, Weng Keeen
dc.date.accessioned2014-01-21T08:19:58Zen
dc.date.accessioned2019-12-06T20:41:41Z-
dc.date.available2014-01-21T08:19:58Zen
dc.date.available2019-12-06T20:41:41Z-
dc.date.copyright2013en
dc.date.issued2013en
dc.identifier.citationKumaran, E., How, K. T. S., Ganguly, R., Li, Y., & Leong, W. K. (2013). Synthesis and reactivity of cationic iridium aminocarbenes derived from terminal alkynes and 2-aminopyridines. Organometallics, 32(15), 4149-4152.en
dc.identifier.urihttps://hdl.handle.net/10356/101625-
dc.description.abstractThe reaction of a terminal alkyne (RCCH) and 2- aminopyridine (R′C5NH3NH2) with the dinuclear species [Cp*IrCl2]2 afforded the cationic aminocarbene derivatives Cp*Ir(Cl)[ C- (CH2R)NHC5NH3R′] via a hydroamination and a ligand substitution. The reaction pathway has been examined through computational studies.en
dc.description.sponsorshipMOE (Min. of Education, S’pore)en
dc.format.extent4p.en
dc.language.isoenen
dc.relation.ispartofseriesOrganometallicsen
dc.rights© 2013 American Chemical Society. This is the author created version of a work that has been peer reviewed and accepted for publication by Organometallics, American Chemical Society. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1021/om400326c].en
dc.subjectDRNTU::Science::Chemistry::Organic chemistry::Organometallic compoundsen
dc.titleSynthesis and reactivity of cationic iridium aminocarbenes derived from terminal alkynes and 2-aminopyridinesen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen
dc.identifier.doi10.1021/om400326cen
dc.description.versionAccepted versionen
item.fulltextWith Fulltext-
item.grantfulltextopen-
Appears in Collections:SPMS Journal Articles
Files in This Item:
File Description SizeFormat 
OM 2013 32 4149.pdf248.57 kBAdobe PDFThumbnail
View/Open

Google ScholarTM

Check

Altmetric


Plumx

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.