AAAAAA

   
Results: 1-13 |
Results: 13
ANTITUMOR-ACTIVITY OF 7-[2-(N-ISOPROPYLAMINO)ETHYL]-(20S)-CAMPTOTHECIN, CKD602, AS A POTENT DNA TOPOISOMERASE-I INHIBITOR
Authors: LEE JH LEE JM KIM JK AHN SK LEE SJ KIM MY JEW SS PARK JG HONG CI
Citation: Jh. Lee et al., ANTITUMOR-ACTIVITY OF 7-[2-(N-ISOPROPYLAMINO)ETHYL]-(20S)-CAMPTOTHECIN, CKD602, AS A POTENT DNA TOPOISOMERASE-I INHIBITOR, Archives of pharmacal research, 21(5), 1998, pp. 581-590
2-CHLORO-4,6-DIMETHOXY-1,3,5-TRIAZINE - A NEW EFFECTIVE AND CONVENIENT COUPLING REAGENT FOR CEPHALOSPORIN DERIVATIVES
Authors: LEE HW KANG TW CHA KH KIM EN CHOI NH KIM JW HONG CI
Citation: Hw. Lee et al., 2-CHLORO-4,6-DIMETHOXY-1,3,5-TRIAZINE - A NEW EFFECTIVE AND CONVENIENT COUPLING REAGENT FOR CEPHALOSPORIN DERIVATIVES, Synthetic communications, 28(8), 1998, pp. 1339-1349
AN EFFECTIVE AND CONVENIENT ESTERIFICATION OF CEPHALOSPORIN DERIVATIVES BY USING QUARTERNARY AMMONIUM-SALTS AS CATALYSTS
Authors: LEE HW KANG TW KIM EN SHIN J CHA KH CHO DO CHOI NH KIM JW HONG CI
Citation: Hw. Lee et al., AN EFFECTIVE AND CONVENIENT ESTERIFICATION OF CEPHALOSPORIN DERIVATIVES BY USING QUARTERNARY AMMONIUM-SALTS AS CATALYSTS, Synthetic communications, 28(23), 1998, pp. 4345-4354
A MILD AND EFFICIENT TETRAHYDROPYRANYLATION OF ALCOHOLS
Authors: CHA KH KANG TW LEE HW KIM EN CHOI NH KIM JW HONG CI
Citation: Kh. Cha et al., A MILD AND EFFICIENT TETRAHYDROPYRANYLATION OF ALCOHOLS, Synthetic communications, 28(12), 1998, pp. 2131-2136
N,N'-DIISOPROPYL-O-DIPHENYLMETHYL ISOUREA - A MILD AND CONVENIENT ALKYLATING AGENT FOR THE FORMATION OF CEPHALOSPORIN DERIVATIVES
Authors: CHA KH KANG TW LEE HW KIM EN CHOI NH KIM JW HONG CI
Citation: Kh. Cha et al., N,N'-DIISOPROPYL-O-DIPHENYLMETHYL ISOUREA - A MILD AND CONVENIENT ALKYLATING AGENT FOR THE FORMATION OF CEPHALOSPORIN DERIVATIVES, Synthetic communications, 28(12), 1998, pp. 2207-2211
DIETHYL CHLOROPHOSPHATE - AN EFFECTIVE AND CONVENIENT COUPLING REAGENT OF CEPHALOSPORIN DERIVATIVES
Authors: LEE HW KANG TW HOI K KIM EN CHOI NH KIM JW HONG CI
Citation: Hw. Lee et al., DIETHYL CHLOROPHOSPHATE - AN EFFECTIVE AND CONVENIENT COUPLING REAGENT OF CEPHALOSPORIN DERIVATIVES, Synthetic communications, 28(1), 1998, pp. 35-44
A PROPOSAL FOR TEMPERATURE COMPENSATION OF THE CIRCADIAN-RHYTHM IN DROSOPHILA BASED ON DIMERIZATION OF THE PER PROTEIN
Authors: HONG CI TYSON JJ
Citation: Ci. Hong et Jj. Tyson, A PROPOSAL FOR TEMPERATURE COMPENSATION OF THE CIRCADIAN-RHYTHM IN DROSOPHILA BASED ON DIMERIZATION OF THE PER PROTEIN, Chronobiology international, 14(5), 1997, pp. 521-529
SYNTHESIS AND STRUCTURE-ACTIVITY RELATIONSHIP OF 2-(5-SUBSTITUTED PYRROLIDIN-4-YLTHIO)-1-BETA-CARBAPENEMS
Authors: LEE HW KIM EN KANG TW AHN SK CHOI NH KIM JW HONG CI
Citation: Hw. Lee et al., SYNTHESIS AND STRUCTURE-ACTIVITY RELATIONSHIP OF 2-(5-SUBSTITUTED PYRROLIDIN-4-YLTHIO)-1-BETA-CARBAPENEMS, Journal of antibiotics, 50(12), 1997, pp. 1078-1082
NUCLEOSIDE CONJUGATES .15. SYNTHESIS AND BIOLOGICAL-ACTIVITY OF ANTI-HIV NUCLEOSIDE CONJUGATES OF ETHER AND THIOETHER PHOSPHOLIPIDS
Authors: HONG CI NECHAEV A KIRISITS AJ VIG R WEST CR MANOUILOV KK CHU CK
Citation: Ci. Hong et al., NUCLEOSIDE CONJUGATES .15. SYNTHESIS AND BIOLOGICAL-ACTIVITY OF ANTI-HIV NUCLEOSIDE CONJUGATES OF ETHER AND THIOETHER PHOSPHOLIPIDS, Journal of medicinal chemistry, 39(9), 1996, pp. 1771-1777
NUCLEOSIDE CONJUGATES .14. SYNTHESIS AND ANTITUMOR-ACTIVITY OF 1-BETA-D-ARABINOFURANOSYLCYTOSINE CONJUGATES OF ETHER LIPIDS WITH IMPROVED WATER SOLUBILITY
Authors: HONG CI NECHAEV A KIRISITS AJ VIG R HUI SW WEST CR
Citation: Ci. Hong et al., NUCLEOSIDE CONJUGATES .14. SYNTHESIS AND ANTITUMOR-ACTIVITY OF 1-BETA-D-ARABINOFURANOSYLCYTOSINE CONJUGATES OF ETHER LIPIDS WITH IMPROVED WATER SOLUBILITY, Journal of medicinal chemistry, 38(10), 1995, pp. 1629-1634
NUCLEOSIDE-ETHER LIPID CONJUGATES AS BIOTRANSFORMED PRODRUGS OF ANTITUMOR AND ANTIVIRAL NUCLEOSIDES
Authors: HONG CI WEST CR BERNACKI RJ CHU CK
Citation: Ci. Hong et al., NUCLEOSIDE-ETHER LIPID CONJUGATES AS BIOTRANSFORMED PRODRUGS OF ANTITUMOR AND ANTIVIRAL NUCLEOSIDES, Journal of lipid mediators and cell signalling, 10(1-2), 1994, pp. 159-161
SYNTHESIS AND ANTITUMOR-ACTIVITY OF 1-BETA-D-ARABINOFURANOSYLCYTOSINECONJUGATES OF OPTICAL ISOMERS OF ETHER AND THIOETHER LIPIDS
Authors: HONG CI AN SH NECHAEV A KIRISITS AJ VIG R WEST CR
Citation: Ci. Hong et al., SYNTHESIS AND ANTITUMOR-ACTIVITY OF 1-BETA-D-ARABINOFURANOSYLCYTOSINECONJUGATES OF OPTICAL ISOMERS OF ETHER AND THIOETHER LIPIDS, Lipids, 28(11), 1993, pp. 1021-1026
NUCLEOSIDE CONJUGATES .13. SYNTHESIS AND ANTITUMOR-ACTIVITY OF 1-BETA-D-ARABINOFURANOSYLCYTOSINE CONJUGATES OF THIOETHER LIPIDS WITH IMPROVED WATER SOLUBILITY
Authors: HONG CI NECHAEV A KIRISITS AJ VIG R WEST CR
Citation: Ci. Hong et al., NUCLEOSIDE CONJUGATES .13. SYNTHESIS AND ANTITUMOR-ACTIVITY OF 1-BETA-D-ARABINOFURANOSYLCYTOSINE CONJUGATES OF THIOETHER LIPIDS WITH IMPROVED WATER SOLUBILITY, Journal of medicinal chemistry, 36(12), 1993, pp. 1785-1790
Risultati: 1-13 |