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|Title:||Synthesis and reactivity of cationic iridium aminocarbenes derived from terminal alkynes and 2-aminopyridines||Authors:||Kumaran, Elumalai
How, Kai Tong Sonia
Leong, Weng Kee
|Keywords:||DRNTU::Science::Chemistry::Organic chemistry::Organometallic compounds||Issue Date:||2013||Source:||Kumaran, 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.||Series/Report no.:||Organometallics||Abstract:||The 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.||URI:||https://hdl.handle.net/10356/101625
|DOI:||http://dx.doi.org/10.1021/om400326c||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].||Fulltext Permission:||open||Fulltext Availability:||With Fulltext|
|Appears in Collections:||SPMS Journal Articles|
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