| 2011 | Synthesis of benzo[3,4]azepino[1,2-b]isoquinolin-9-ones from 3-arylisoquinolines via ring closing metathesis and evaluation of topoisomerase i inhibitory activity, cytotoxicity and docking study | 권영주 | Article |
| 2006 | Synthesis of benzo[b]benzo[2,3-d]thiophen-6,9-diones via palladium(II) acetate-mediated cyclization of 5-arylthiocyclohexa-2,5-diene-1,4-diones | 유충규 | Article |
| 2005 | Synthesis of benzo[b]naphtho[2,3-d]thiophene-6,11-diones via palladium(II) acetate-mediated cyclization of 3-arylthio-1,4-naphthoquinone | 유충규 | Article |
| 2014 | Synthesis of benzofuro[6,7-d]thiazoles, benzofuro[7,6-d]thiazoles and 6-arylaminobenzo[d]thiazole-4,7-diones as antifungal agent | 유충규 | Article |
| 2010 | Synthesis of benzoxazole amides as novel antifungal agents against Malassezia furfur | 박혜영 | Article |
| 2017 | Synthesis of benzoxazole derivatives as interleukin-6 antagonists | 박혜영; 황은숙 | Article |
| 2012 | Synthesis of biodegradable poly(ε-caprolactone)-organosiloxane hybrid with carboxylate groups | 이승진 | Article |
| 2007 | Synthesis of conformationally locked methanocarba-uridine as a precursor for nucleotides agonizing P2Y6 receptor | 류재상 | 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 |
| 2009 | Synthesis of isoquinolinone-based tetracycles as poly (ADP-ribose) polymerase-1 (PARP-1) inhibitors | 박혜영; 권영주 | Article |
| 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 |
