| 2000 | A highly efficient synthesis of L-β-2′-deoxy-4′-thio-1′-purine nucleosides as potential antiviral agents | 김길수; 정낙신 | Article |
| 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 cyclopropyl-fused 2′-C-methylcarbanucleosides as potential anti-HCV agents | 이강만; 이승진; 신윤용; 정낙신 | Article |
| 2006 | Asymmetric synthesis of homo-apioneplanocin A from d-ribose | 이강만; 정낙신 | Article |
| 2007 | Asymmetric synthesis of novel apio carbocyclic nucleoside analogues as potential antiviral and antitumor agent | 이강만; 정낙신 | Conference Paper |
| 2007 | Asymmetric synthesis of novel pseudo-D-vinylcyclopropyl nucleosides bearing quaternary carbon as potential anti-herpesvirus agent | 정낙신 | Article |
| 2005 | D-4′-thioadenosine derivatives as highly potent and selective agonists at the human A3 adenosine receptor | 정낙신 | Conference Paper |
| 2004 | Design and synthesis of 3′-ureidoadenosine-5′-uronamides: Effects of the 3′-ureido group on binding to the A 3 adenosine receptor | 정낙신 | Article |
| 2003 | Design and synthesis of A3 adenosine receptor ligands, 2′-fluoro analogues of Cl-IB-MECA | 정낙신 | Conference Paper |
| 2003 | Design and synthesis of A3 adenosine receptor ligands, 3′-fluoro analogues of Cl-IB-MECA | 정낙신 | Conference Paper |
| 2007 | Design, enantiopure synthesis, and biological evaluation of novel ISO-D-2′,3′-dideoxy-3′-fluorothianucleoside derivatives as a bioisostere of lamivudine | 정낙신 | Article |
| 2003 | Design, synthesis and binding affinity of 3′-fluoro analogues of Cl-IB-MECA as adenosine A3 receptor ligands | 이승진; 정낙신 | Article |
| 2007 | Design, synthesis, and anti-tumor activity of 4′-thionucleosides as potent and selective agonists at the human A3 adenosine receptor | 정낙신; 이상국 | Article |
| 2006 | Design, synthesis, and biological activity of N6-substituted-4′-thioadenosines at the human A3 adenosine receptor | 정낙신; 이상국 | Article |
| 2003 | Design, synthesis, and biological evaluation of fluoroneplanocin A as the novel mechanism-based inhibitor of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | Article |
| 2007 | Design, synthesis, and biological evaluation of novel iso-d-2′,3′-dideoxy-3′-fluorothianucleoside derivatives | 정낙신 | Article |
| 2003 | Design, synthesis, and in vitro evaluation of APIO analogue of neplanocin A | 정낙신 | Conference Paper |
| 2005 | Development of potent and selective human A3 adenosine receptor agonists. | 정낙신; 이상국 | Article |
| 2003 | N6-substituted D-4′-thioadenosine-5′-methyluronamides: Potent and selective agonists at the human A3 adenosine receptor | 정낙신 | Article |
| 1998 | Participation of sulfur occurred during the Mitsunobu reaction: Synthesis of novel isodideoxythionucleosides | 정낙신 | Article |
| 1998 | Ring contraction and rearrangement of 4-thiofuranose derivatives observed during dast fluorination in the synthesis of L-2'-'up'-fluoro-4'- thiothymidine | 정낙신 | Article |
| 2007 | Stereoselective synthesis of 1′-functionalized-4′- thionucleosides | 정낙신 | Article |
| 2005 | Stereoselective synthesis of 3-hydroxymethyl-D-cyclopentenone, the versatile intermediate for the synthesis of carbocyclic nucleosides | 이강만; 신윤용; 정낙신 | Conference Paper |
| 2002 | Stereoselective synthesis of a novel apio analogue of neplanocin A as potential S-adenosylhomocysteine hydrolase inhibitor | 이강만; 정낙신 | Article |
| 2002 | Stereoselective synthesis of amino-substituted apio dideoxynucleosides through a distant neighboring group effect | 정낙신 | Article |
| 2005 | Stereoselective synthesis of conformationally rigid apio carbanucleosides as potential antiviral agents | 정낙신 | Conference Paper |
| 2007 | Stereoselective synthesis of homo-apioneplanocin A as potential inhibitor of S-adenosylhomocysteine hydrolase | 이강만; 정낙신 | Conference Paper |
| 2005 | Stereoselective synthesis of novel thioiso dideoxy nucleosides with exocyclic methylene as potential antiviral agents | 정낙신 | Conference Paper |
| 2005 | Structure-activity relationship of 5′-substituted fluoro-neplanocin A analogues as potent inhibitors of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | Conference Paper |
