| 2017 | N6-Substituted 5′-N-Methylcarbamoyl-4′-selenoadenosines as Potent and Selective A3 Adenosine Receptor Agonists with Unusual Sugar Puckering and Nucleobase Orientation | 최선 | Article |
| 2003 | N6-substituted D-4′-thioadenosine-5′-methyluronamides: Potent and selective agonists at the human A3 adenosine receptor | 정낙신 | Article |
| 2013 | Neddylation pathway regulates the proliferation and survival of macrophages | 정낙신 | Article |
| 2013 | New RNA purine building blocks, 4'-selenopurine nucleosides: First synthesis and unusual mixture of sugar puckerings | 정낙신; 최원준 | Article |
| 2006 | Nucleoside prodrugs of A3 adenosine receptor agonists and antagonists | 정낙신 | Article |
| 2009 | Nucleoside-based adenosine A3 receptor antagonists as drug candidates | 정낙신 | Review |
| 2010 | Nucleoside-derived antagonists to A3 adenosine receptors lower mouse intraocular pressure and act across species | 정낙신 | Article |
| 2006 | Orthogonal activation of the reengineered A3 adenosine receptor (neoceptor) using tailored nucleoside agonists | 정낙신 | Article |
| 2014 | Overactivated neddylation pathway as a therapeutic target in lung cancer | 정낙신 | Article |
| 1998 | Participation of sulfur occurred during the Mitsunobu reaction: Synthesis of novel isodideoxythionucleosides | 정낙신 | Article |
| 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 4′-thionucleosides as potential antiviral and antitumor agents | 정낙신 | Review |
| 2013 | Recent Advances in Synthesis and Biological Activity of 4'-Thionucleosides | 정낙신 | Chapter |
| 2014 | Recent advances in the synthesis of carbocyclic nucleosides via ring-closing metathesis | 정낙신 | Review |
| 2004 | Recent advances in the synthesis of the carbocyclic nucleosides as potential antiviral agents | 정낙신 | Review |
| 2011 | Regio- and stereoselective synthesis of truncated 3′- aminocarbanucleosides and their binding affinity at the A 3 adenosine receptor | 정낙신; 최원준 | Article |
| 2011 | Renoprotective antioxidant effect of alagebrium in experimental diabetes | 정낙신; 하헌주; 최원준 | 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 | Role of adenosine A3 receptors on CA1 hippocampal neurotransmission during oxygen-glucose deprivation episodes of different duration | 정낙신 | Article |
| 2008 | Selective A3 adenosine receptor antagonists derived from nucleosides containing a bicyclo[3.1.0]hexane ring system | 정낙신 | Article |
| 2019 | Small-molecule inhibitor of HlyU attenuates virulence of Vibrio species | 김병식 | Article |
| 2011 | Stereoselective amination of chiral benzylic ethers using chlorosulfonyl isocyanate: Total synthesis of (+)-Sertraline | 정낙신 | Article |
| 2012 | Stereoselective synthesis and anti-HCV activity of conformationally restricted 2′-C-substituted carbanucleosides | 정낙신; 최원준 | 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 |
| 2012 | Stereoselective synthesis of fluoro-homoneplanocin A as a potential antiviral agent | 정낙신 | Article |
| 2007 | Stereoselective synthesis of homo-apioneplanocin A as potential inhibitor of S-adenosylhomocysteine hydrolase | 이강만; 정낙신 | Conference Paper |
