2007 | Asymmetric synthesis and biological activity of l-bicyclocarba-d4T | 정낙신 | Article |
2007 | Asymmetric synthesis of apio fluoroneplanocin a analogs as potential AdoHcy hydrolase inhibitor | 정낙신 | Article |
2007 | Asymmetric synthesis of novel pseudo-D-vinylcyclopropyl nucleosides bearing quaternary carbon as potential anti-herpesvirus agent | 정낙신 | Article |
2008 | Design and synthesis of 5''-iodoneplanocin a and its analogues as potential S-adenosylhomocysteine hydrolase inhibitor | 정낙신 | Article |
2007 | Design, enantiopure synthesis, and biological evaluation of novel ISO-D-2′,3′-dideoxy-3′-fluorothianucleoside derivatives as a bioisostere of lamivudine | 정낙신 | Article |
2007 | Design, synthesis, and biological evaluation of novel iso-d-2′,3′-dideoxy-3′-fluorothianucleoside derivatives | 정낙신 | Article |
2009 | Design, synthesis, antitumor activity and mode of action of novel oxiranyl and thiiranyl phenol derivatives | 정낙신 | Article |
2009 | Efficient and practical synthesis of l-hamamelose | 정낙신 | Article |
2010 | First synthesis of 2′-oxabicyclo[3.1.0]hexyl nucleosides with a north conformation | 정낙신 | Article |
2009 | Highly concise synthesis of 3'-"up"-ethynyl-5'-methylbicyclo- [3.1.0]hexyl purine and pyrimidine nucleoside derivatives using rhodium(II) carbenoid cycloaddition and highly diastereoselective Grignard reaction | 정낙신 | Article |
2005 | Layered double hydroxide surface modified with (3-aminopropyl) triethoxysilane by covalent bonding | 김성진; 우애자 | Article |
2007 | Synthesis of enantiopure pseudo-L-vinylcyclopropyl nucleosides bearing quaternary carbon as potential anti-herpesvirus agent | 정낙신 | Article |
2008 | Synthesis of methyl-substituted bicyclic carbanucleoside analogs as potential antiherpetic agents | 정낙신 | Article |
2009 | Synthesis of neplanocin a analog with 2′′-"up"-C-methyl substituent as potential anti-HCV Agent | 정낙신 | Article |
2006 | Synthesis of novel l-N-MCd4T as a potent anti-HIV agent | 정낙신 | Article |