dc.contributor.authorLim, Maricar Bungabong
dc.date.accessioned2009-12-23T05:57:19Z
dc.date.accessioned2017-07-23T08:43:12Z
dc.date.available2009-12-23T05:57:19Z
dc.date.available2017-07-23T08:43:12Z
dc.date.copyright2008en_US
dc.date.issued2008
dc.identifier.citationLim, M. B. (2008). Asymmetric synthesis of chiral arsine ligands promoted by organopalladium complexes. Doctoral thesis, Nanyang Technological University, Singapore.
dc.identifier.urihttp://hdl.handle.net/10356/20676
dc.description.abstractThe bis(acetonitrile) (S) phenanthrylamine palladium II complex (Sc)-116 is used in the [4+2] Diels-Alder cycloaddition reaction between diphenylvinylarsine and DMPP producing two isomeric products in a ratio of 5:1. The bidentate ligand (Sp)-80 is liberated by simple treatment of complex (Rp)-79 with aqueous potassium cyanide.en_US
dc.format.extent283 p.en_US
dc.language.isoenen_US
dc.subjectDRNTU::Science::Chemistry::Organic chemistry::Organometallic compoundsen_US
dc.subjectDRNTU::Science::Chemistry::Organic chemistry::Organic synthesis
dc.titleAsymmetric synthesis of chiral arsine ligands promoted by organopalladium complexesen_US
dc.typeThesis
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.contributor.supervisorLeung Pak Hing (SPMS)en_US
dc.description.degreeDOCTOR OF PHILOSOPHY (SPMS)en_US


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