| 2005 | Synthesis of 3'-ureidoadenosines and their high binding affinity at the mutant A3 adenosine receptor. | 이강만; 정낙신 | Article |
| 2008 | Synthesis of 3′-acetamidoadenosine derivatives as potential A 3 adenosine receptor agonists | 정낙신; 최원준 | Article |
| 2010 | Synthesis of 3′-Azido-2′, 3′-dideoxy-4′-selenouridine As Potential Anti-HIV Agent | 전정하 | Master's Thesis |
| 2005 | Synthesis of 3′-deoxy-3′-C-hydroxymethyl analogues of tiazofurin and ribavirin | 정낙신 | Conference Paper |
| 2005 | Synthesis of 3′-ureidoadenosine analogues and their binding affinity to the A3 adenosine receptor | 정낙신 | Conference Paper |
| 2003 | Synthesis of 5-Azacytidine nucleosides with rigid sugar moiety as potential antitumor agents | 정낙신 | Conference Paper |
| 2004 | Synthesis of 5′-substituted fluoro-neplanocin A analogues: Importance of a hydrogen bonding donor at 5′-position for the inhibitory activity of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | Article |
| 2003 | Synthesis of [1′-fluoro-2′,2′ -bis-(hydroxymethyl)-cyclopropylmethyl]purines as antiviral agents | 정낙신 | Conference Paper |
| 2004 | Synthesis of apio analogues of neplanocin a and their inhibitory activity against S-adenosylhomocysteine hydrolase. | 정낙신 | Meeting Abstract |
| 2003 | Synthesis of apio analogues of neplanocin A as potential inhibitors of S-adenosylhomocysteine hydrolase. | 정낙신 | Article |
| 2012 | Synthesis of Biologically Active Nucleosides | 남수경 | Master's Thesis |
| 2011 | Synthesis of Carbocyclic Nucleosides as Potent Antiviral and Antitumor Agents | 박진영 | Master's Thesis |
| 1999 | Synthesis of cyclopropyl-fused carbocyclic nucleosides via the regioselective opening of cyclicsulfi sulfites | 정낙신 | Article |
| 2004 | Synthesis of D- and L-apio nucleoside analogues with 2′-hydroxyl group as potential anti-HIV agents | 정낙신; 김대기 | Article |
| 2007 | Synthesis of enantiopure pseudo-L-vinylcyclopropyl nucleosides bearing quaternary carbon as potential anti-herpesvirus agent | 정낙신 | Article |
| 2004 | Synthesis of fluorinated cyclopentenyladenine as potent inhibitor of S-adenosylhomocysteine hydrolase | 이강만; 정낙신 | Article |
| 2008 | Synthesis of fluoroneplanocin A | 정낙신; 최원준 | Review |
| 2008 | Synthesis of fluoroneplanocin A. | 정낙신; 최원준 | Article |
| 2003 | Synthesis of halogenated 9-(dihydroxycyclopent-4′-enyl) adenines and their inhibitory activities against S-Adenosylhomocysteine hydrolase | 정낙신 | Conference Paper |
| 2005 | Synthesis of homo-N-nucleoside with 1,2,4-triazole-3-carboxamide | 정낙신 | Conference Paper |
| 1999 | Synthesis of L-sangivamycin and toyocamycin analogues and their inhibitory activities of Ser/Thr protein kinases | 정낙신 | Conference Paper |
| 2008 | Synthesis of methyl-substituted bicyclic carbanucleoside analogs as potential antiherpetic agents | 정낙신 | Article |
| 2007 | Synthesis of N6-Substituted 3′-ureidoadenosine derivatives as highly potent agonists at the mutant A3 adenosine receptor | 정낙신 | Conference Paper |
| 2004 | Synthesis of N^(6)-Substituted-5'-Hydroxymethyl-D-4'-Thioadenosine Derivatives As Potential A₃Adenosine Receptor Agonists | 정지영 | Master's Thesis |
| 2009 | Synthesis of neplanocin a analog with 2′′-"up"-C-methyl substituent as potential anti-HCV Agent | 정낙신 | Article |
| 2002 | Synthesis of novel (2R,4R)- and (2S,4S)-iso dideoxynucleosides with exocyclic methylene as potential antiviral agents | 정낙신 | Article |
| 2001 | Synthesis of novel 3 '-deoxy-3 '-C-hydroxymethyl nucleosides with conformationally rigid sugar moiety as potential antiviral agents | 정낙신 | Article; Proceedings Paper |
| 2005 | Synthesis of novel apio carbocyclic nucleoside analogues as selective A3 adenosine receptor agonists | 이강만; 정낙신 | Article |
| 2001 | Synthesis of novel D- and L-3 '-deoxy-3 '-C-hydroxymethyl nucleoside with exocyclic methylene as potential ribonucleotide reductase inhibitor | 정낙신 | Article; Proceedings Paper |
| 2002 | Synthesis of novel D-2′-Deoxy-2′-C-difluoromethylene-4′-thiocytidine as a potential antitumor agent | 정낙신 | Article |
