| 2004 | Synthesis and biological evaluation of novel tert-azido or ten-amino substituted penciclovir analogs | 정낙신; 김대기 | Article |
| 2002 | Synthesis and biological evaluation of novel thioapio dideoxynucleosides | 정낙신; 이상국; 최원준 | Article |
| 2003 | Synthesis and biological evaluation of pyrimidine nucleosides fused with 3′,4′-tetrahydrofuran ring | 정낙신 | Conference Paper |
| 2003 | Synthesis and biological evaluation of thymine nucleosides fused with 3′,4′-tetrahydrofuran ring | 정낙신 | Article |
| 2008 | Synthesis and conformational analysis of novel 2',3'-didehydo-2',3'-dideoxy-4'-selenonucleosides. | 정낙신; 최원준 | Article |
| 1999 | Synthesis and hybridization property of sugar and phosphate linkage modified oligonucleotides | 정낙신 | Article |
| 2008 | Synthesis and structure-activity relationship studies of tyrosine-based antagonists at the human P2X7 receptor | 정낙신 | Article |
| 2000 | Synthesis of (-)-Neplanocin A Analogues as Potential Antiviral Agents | 정낙신 | Article |
| 2003 | Synthesis of (Z)-(1-fluoro-2-hydroxymethyl-cyclopropylmethyl)purines | 정낙신 | Conference Paper |
| 2003 | Synthesis of 2-(3′-Azido- and 3′-Amino-3′-deoxy-β -D-ribofuranosyl)thiazole-4-carboxamide | 정낙신 | Article |
| 2008 | Synthesis of 2-alkynyl substituted 4′-thioadenosine derivatives and their binding affinities at the adenosine receptors | 정낙신; 최원준 | Article |
| 2006 | Synthesis of 2-C-hydroxymethylribofuranosylpurines as potent anti-hepatitis C virus (HCV) agents | 이강만; 정낙신 | Article |
| 2008 | Synthesis of 2-chloro-N6-substituted-4'-thioadenosine-5'-N, N-dialkyluronamides as potent and selective A3 adenosine receptor antagonists. | 정낙신; 최원준 | Article |
| 2008 | Synthesis of 3'-C-hydroxymethyl-substituted pyrimidine and purine nucleosides as potential anti-hepatitis C virus (HCV) agents | 정낙신; 최원준 | Article |
| 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 |
| 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 |
| 2003 | Synthesis of apio analogues of neplanocin A as potential inhibitors of S-adenosylhomocysteine hydrolase. | 정낙신 | Article |
| 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 |
