dc.contributor.authorGao, Qi
dc.date.accessioned2010-04-23T00:51:26Z
dc.date.accessioned2017-07-23T08:25:27Z
dc.date.available2010-04-23T00:51:26Z
dc.date.available2017-07-23T08:25:27Z
dc.date.copyright2010en_US
dc.date.issued2010
dc.identifier.citationGao, Q. (2010). Novel 1,1'-bisisoquinolines : synthesis, resolution and application in asymmetric catalysis. Doctoral thesis, Nanyang Technological University, Singapore.
dc.identifier.urihttp://hdl.handle.net/10356/35690
dc.description.abstractThis thesis deals with the chemistry of novel 1,1'-bisisoquinolines and derivatives. Application of enantiopure 1,1'-bisisoquinolines as ligands for various asymmetric C-C bond forming reactions has been examined. Condition for the preparation of the anticipated 1,1'-bisisoquinolines has been established. Racemic C2-symmetric 1,1'-bisisoquinolines and pseudo symmetric 1,1'-bisisoquinolines were synthesized through classical double Bischler-Napieralski reaction followed by reduction with borohydrides. Racemic pseudo symmetric 1,1'-bisisoquinoline could also be synthesized directly through double Bischler-Napieralski reaction using polyphosphoric acid at elevated temperatures. Resolution of the racemic 1,1'-bisisoquinolines via diastereomeric salt and covalent bond formation was explored thoroughly. Diasteromeric salts failed to separate to give individual enantiomers. Covalent bond formation using chiral isocyanates such as α-methylbenzyl isocyanate gave diastereomeric urea derivatives that were separated by a combination of column chromatography and recrystallization techniques. Acid and base catalyzed alcoholysis approaches were explored to obtain the free enantiopure 1,1'-bisisoquinolines. Difficulties were met during the alcoholysis mainly due to racemization of the enantiomers. However, after optimization of the reaction conditions, base alcoholysis followed by recrystallization gave the required 1,1'-bisisoquinoline in enantiopure form. The reactivity and structural features of (+)-1,2,3,4-tetrahydro- -1,1'-bisisoquinoline were explored in details through formation of various N-alkyl, amide, urea and thiourea derivatives and by studying the X-ray structures of some of these derivatives.en_US
dc.format.extent297 p.en_US
dc.language.isoenen_US
dc.subjectDRNTU::Engineering::Chemical engineering::Biochemical engineeringen_US
dc.titleNovel 1,1'-bisisoquinolines : synthesis, resolution and application in asymmetric catalysisen_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


Files in this item

FilesSizeFormatView
GaoQi2010.pdf32.87Mbapplication/pdfView/Open

This item appears in the following Collection(s)

Show simple item record