| 2005 | A highly efficient synthesis of unnatural L-sugars from D-ribose | 정낙신; 최원준 | Article |
| 2007 | Discovery of a new nucleoside template for human A3 adenosine receptor ligands: D-4′-thioadenosine derivatives without 4′-hydroxymethyl group as highly potent and selective antagonists | 정낙신; 이상국 | Article |
| 2009 | Discovery of a new template for anticancer agents: 2′-deoxy-2′- fluoro-4′-selenoarabinofuranosyl-cytosine (2′-F-4′-seleno-ara- C) | 정낙신; 이상국; 최선; 최원준 | Article |
| 2008 | First synthesis of 4′-selenonucleosides showing unusual southern conformation | 정낙신; 이상국; 권영주 | Article |
| 2004 | Preparative synthesis of the key intermediate, (4R,5R)-3-Benzyloxymethyl-4, 5-isopropylidenedioxycyclopent-2-enone for carbocyclic nucleosides | 정낙신 | Article |
| 2007 | Probing the binding site of the A1 adenosine receptor reengineered for orthogonal recognition by tailored nucleosides | 정낙신 | Article |
| 2006 | Stereoselective functionalization of the 1′-position of 4′-thionucleosides | 정낙신; 최선; 류재상 | Article |
| 2008 | Stereoselective synthesis and conformational study of novel 2′,3′-didehydro-2′,3′-dideoxy-4′-selenonucleosides | 정낙신; 최선; 최원준 | Article |
| 2006 | Stereoselective synthesis of 2′-C-methyl-cyclopropyl-fused carbanucleosides as potential anti-HCV agents | 정낙신 | Article |
| 2008 | Structure-activity relationships of truncated D- and L-4′- thioadenosine derivatives as species-independent A3 adenosine receptor antagonists | 정낙신; 이상국; 최원준 | Article |
