2003 | N6-substituted D-4′-thioadenosine-5′-methyluronamides: Potent and selective agonists at the human A3 adenosine receptor | 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 | Rearrangement of tryptophan residues in caspase-3 active site upon activation | 이민영 | Article |
2004 | Recent advances in 4′-thionucleosides as potential antiviral and antitumor agents | 정낙신 | Review |
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 |
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 |
2005 | Stereoselective synthesis of conformationally rigid apio carbanucleosides as potential antiviral agents | 정낙신 | Conference Paper |
2007 | Stereoselective synthesis of homo-apioneplanocin A as potential inhibitor of S-adenosylhomocysteine hydrolase | 이강만; 정낙신 | Conference Paper |
2004 | Structural determinants of efficacy at A3 adenosine receptors: Modification of the ribose moiety | 정낙신 | Article |
2005 | Structure-activity relationship of 5′-substituted fluoro-neplanocin A analogues as potent inhibitors of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | 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 |
2001 | Structure-activity relationships of apio nucleosides as potential antiviral agents | 정낙신 | Conference Paper |
1997 | Syntheses and antiviral activities of 1,3-dioxolanyl-, 1,3-oxathiolanyl- and 1,3-dithiolanylnucleosides with 2-hydroxymethyl substituents | 정낙신 | Article |
2007 | Synthesis and anti-HCV activity of 2′-β-hydroxymethylated nucleosides | 이강만; 정낙신 | Conference Paper |
2007 | Synthesis and antitumor activity of fluorocyclopentenyl-pyrimidines | 정낙신; 이상국 | Conference Paper |
1999 | Synthesis and antiviral activities of 1,3-oxathiolanyl nucleosides with 5-hydroxymethyl substituent | 정낙신 | Conference Paper |
1998 | Synthesis and antiviral activity of apio dideoxy nucleosides with azido or amino substituent | 정낙신 | Article |
1999 | Synthesis and antiviral activity of D- and L-isodideoxy nucleosides with exocyclic methylene | 정낙신 | Conference Paper |
2001 | Synthesis and Antiviral Activity of Fluoro-substituted Apio Dideoxynucleosides | 정낙신 | Article |
1999 | Synthesis and antiviral activity of L-2'-deoxy-2'-up-fluoro-4'- thionucleosides | 정낙신 | Conference Paper |
2003 | Synthesis and biological evaluation of halo-neplanocin A as novel mechanism-based inhibitors of S-Adenosylhomocysteine hydrolase | 정낙신 | Conference Paper |
2002 | Synthesis and biological evaluation of novel D-2′-azido-2′,3′-dideoxyarabinofuranosyl-4′- thiopyrimidines and purines | 정낙신 | Article |
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 |
1999 | Synthesis and hybridization property of sugar and phosphate linkage modified oligonucleotides | 정낙신 | Article |