dc.contributor.authorYao, Qiong Ji
dc.date.accessioned2012-08-27T07:02:54Z
dc.date.accessioned2017-07-23T08:25:55Z
dc.date.available2012-08-27T07:02:54Z
dc.date.available2017-07-23T08:25:55Z
dc.date.copyright2012en_US
dc.date.issued2012
dc.identifier.citationYao, Q. J. (2012). Novel bisisoquinolines : synthesis, resolution and application in asymmetric Henry reaction. Doctoral thesis, Nanyang Technological University, Singapore.
dc.identifier.urihttp://hdl.handle.net/10356/50660
dc.description.abstractThis research project presented in this thesis focuses on the synthesis of enantiopure novel 1,3-diposed and classical 1,2-diposed bisisoquinolines, and application of those bisisoquinolines as ligands for one powerful C-C bond formation reaction―Henry reaction. Condition for synthesis of the anticipated 1,3-disposed bisisoquinolines and its derivatives have been established. Racemic symmetric 1,3-disposed bisisoquinolines was prepared through classical double Bischler-Napieralski reaction followed by reduction with Sodium cyanoborohydride. Resolution of the racemic symmetric 1,3-disposed bisisoquinolines to afford individual enantiomers was solved via diastereomeric salt formation with (L)-(+)-citramalic acid. The absolute configuration of this novel 1,3-diamine 1,1’-methylene-bis(1,1’,2,2’,3,3’,4,4’-octahydroisoquinoline) was established by X-Ray crystallography. Mono-, di- and bridged N-alkyl derivatives based on racemic, (R,R)-parent compound were synthesized to explore this 1,3-diposed bisisoquinolines’ chemistry. Application of the enantiopure 1,3- and 1,2-diposed bisisoquinolines in catalysis of asymmetric henry reaction was examined, C1-1’,2’,3’,4’-terahydro-1,1’-bisisoquinoline’s copper(I) complex proved to be the most efficient catalyst for the enantioselective Henry reaction between aldehydes and nitromethane. β-nitroalcohol adducts were obtained in high yields and enatioselectivities. This catalyst system was simple in operation since no special precautions were taken to exclude moisture or air from the reaction flask. (R)-N-alkyl-C1-1’,2’,3’,4’-terahydro-1,1’-bisisoquinoline differing in the steric bulkiness were successfully afforded to be examined in the asymmetric Henry reaction. The ligand bearing the smallest substituent was proved to be the most effective one in the CuI-catalyzed addition of nitromethane, nitroethane and nitropropane to aldehydes. Excellent catalytic results were achieved in this thesis, represented a major contribution to the application of bisisoquinolines as ligands in asymmetric catalysis of Henry reaction.en_US
dc.format.extent276 p.en_US
dc.language.isoenen_US
dc.subjectDRNTU::Engineering::Chemical engineeringen_US
dc.titleNovel bisisoquinolines : synthesis, resolution and application in asymmetric Henry reactionen_US
dc.typeThesis
dc.contributor.schoolSchool of Chemical and Biomedical Engineeringen_US
dc.contributor.supervisorZaher Judehen_US
dc.description.degreeDOCTOR OF PHILOSOPHY (SCBE)en_US


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