Back to results list
Please use this identifier to cite or link to this item:
|Title:||Quinoline-type compounds : asymmetric catalytic reaction and their biological activities||Authors:||Chan, Sau Hing||Keywords:||Quinoline.
Hong Kong Polytechnic University -- Dissertations
|Issue Date:||2013||Publisher:||The Hong Kong Polytechnic University||Abstract:||The dipyridinyl phosphine ligand P-Phos was proven to be effective for many catalytic reactions. Herein the iridium-complex catalyzed asymmetric hydrogenation of 8-hydroxyquinoline substrates with the newly synthesized dipyridinyl phosphine type ligands was investigated. The electronic properties of the dipyridinyl phosphine type ligands had a significant effect on the enantioselectivities of 8-substituted 1,2,3,4-tetrahydroquinoline compounds. High enantioselectivities were observed for most 8-substituted quinoline compounds with ligands containing the electron-donating OMe group at the para-position with ee up to 96%. However, lower enantioselectivities were obtained with ligands containing the electron-withdrawing CF3 group at the para-position. Asymmetric transfer hydrogenation could be an alternative method to produce optically active compounds. In this project, the efficiency of easily synthesized chiral quinoline-based ligand 1-((1R,2R)-2-aminocyclohexyl)-3-(quinolin-8-yl)urea has been evaluated in the ruthenium catalyzed asymmetric transfer hydrogenation of aromatic ketones in isopropanol with ee up to 84%. This catalyst could be recovered and reused in room temperature ionic liquid and polyethylene glycol at least five times with no significant loss of enantioselectivities. The quinoline derivatives and their possible cytotoxic potential towards human cancer cell lines were described in this project. 8-Hydroxy-2-quinolinecarbaldehyde, 2-methyl-1,2,3,4-tetrahydroquinolin-8-ol, 2-methyl-8-(4-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydroquinoline, and 5,7-dibromo-2-methyl-1,2,3,4-tetrahydroquinolin-8-ol showed the best in vitro cytotoxicity against a plane of human cancer cell lines that include MDA231, T-47D, Hs578t, SaoS2, K562, SKHep, Hep3B, KYSE150, HKESC-3, HKESC-4 and MCF-7 with MTS50 range of 3.1-12.5μg/ml. The experimental results showed that these quinoline compounds were potential anti-tumor agents. Further in vivo results showed that the dosage of 5-10mg/kg/day (i.p. injection for 9 to 20 days) could completely abolish the growth of the Hep3B hepatocellular and KYSE150 esophageal tumor xenograft on athymic nude mice model compared with the control, with no damage to vital organs at the histological level.||Description:||xviii, 321 p. : ill. ; 30 cm.
PolyU Library Call No.: [THS] LG51 .H577P ABCT 2013 Chan
|URI:||http://hdl.handle.net/10397/6471||Rights:||All rights reserved.|
|Appears in Collections:||Thesis|
Show full item record
Files in This Item:
|b26527224_link.htm||For PolyU Users||203 B||HTML||View/Open|
|b26527224_ir.pdf||For All Users (Non-printable)||16.76 MB||Adobe PDF||View/Open|
Citations as of Oct 15, 2018
Citations as of Oct 15, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.