| 2007 | Asymmetric synthesis of cyclopropyl-fused 2′-C-methylcarbanucleosides as potential anti-HCV agents | 이강만; 이승진; 신윤용; 정낙신 | Article |
| 2007 | Asymmetric synthesis of novel apio carbocyclic nucleoside analogues as potential antiviral and antitumor agent | 이강만; 정낙신 | Conference Paper |
| 2005 | Design, synthesis, and anticancer activity of fluorocyclopentenyl-pyrimidines. | 이강만; 정낙신; 이상국; 최원준 | 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 in vitro evaluation of APIO analogue of neplanocin A | 정낙신 | Conference Paper |
| 2004 | Preparative and Stereoselective Synthesis of the Versatile Intermediate for Carbocyclic Nucleosides: Effects of the Bulky Protecting Groups to Enforce Facial Selectivity | 정낙신 | Article |
| 2004 | Recent advances in the synthesis of the carbocyclic nucleosides as potential antiviral agents | 정낙신 | Review |
| 2006 | Stereoselective synthesis of 2′-C-methyl-cyclopropyl-fused carbanucleosides as potential anti-HCV agents | 정낙신 | Article |
| 2005 | Stereoselective synthesis of 3-hydroxymethyl-D-cyclopentenone, the versatile intermediate for the synthesis of carbocyclic nucleosides | 이강만; 신윤용; 정낙신 | Conference Paper |
| 2006 | Structure-activity relationships of 2-chloro-N6-substituted- 4′-thioadenosine-5′-uronamides as highly potent and selective agonists at the human A3 adenosine receptor | 정낙신; 이상국 | Article |
| 2008 | Syntheses and Biological Activity of Neplanocin and Analogues | 정낙신 | Chapter |
| 2008 | Synthesis and biological evaluation of trisubstituted imidazole derivatives as inhibitors of p38α mitogen-activated protein kinase | 김대기 | Article |
| 2003 | Synthesis of apio analogues of neplanocin A as potential inhibitors of S-adenosylhomocysteine hydrolase. | 정낙신 | Article |
| 2005 | Synthesis of novel apio carbocyclic nucleoside analogues as selective A3 adenosine receptor agonists | 이강만; 정낙신 | Article |
