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Results: 1-13 |
Results: 13
Synthesis and application of dimeric Cinchona alkaloid phase-transfer catalysts: alpha,alpha '-bis[O(9)-allylcinchonidinium]-o, m, or p-xylene dibromide
Authors: Jew, SS Jeong, BS Yoo, MS Huh, H Park, HG
Citation: Ss. Jew et al., Synthesis and application of dimeric Cinchona alkaloid phase-transfer catalysts: alpha,alpha '-bis[O(9)-allylcinchonidinium]-o, m, or p-xylene dibromide, CHEM COMMUN, (14), 2001, pp. 1244-1245
Trimeric Cinchona alkaloid phase-transfer catalyst: alpha,alpha ',alpha ''-tris[O(9)-allylcinchonidinium]mesitylene tribromide
Authors: Park, HG Jeong, BS Yoo, MS Park, MK Huh, H Jew, SS
Citation: Hg. Park et al., Trimeric Cinchona alkaloid phase-transfer catalyst: alpha,alpha ',alpha ''-tris[O(9)-allylcinchonidinium]mesitylene tribromide, TETRAHEDR L, 42(28), 2001, pp. 4645-4648
Asiatic acid derivatives protect cultured cortical neurons from glutamate-induced excitotoxicity
Authors: Lee, MK Kim, SR Sung, SH Lim, DY Kim, H Choi, H Park, HK Jew, SS Kim, YC
Citation: Mk. Lee et al., Asiatic acid derivatives protect cultured cortical neurons from glutamate-induced excitotoxicity, RES COM M P, 108(1-2), 2000, pp. 75-86
Structure-activity relationship study of asiatic acid derivatives against beta amyloid (A beta)-induced neurotoxicity
Authors: Jew, SS Yoo, CH Lim, DY Kim, H Mook-Jung, I Jung, MW Choi, H Jung, YH Kim, H Park, HG
Citation: Ss. Jew et al., Structure-activity relationship study of asiatic acid derivatives against beta amyloid (A beta)-induced neurotoxicity, BIOORG MED, 10(2), 2000, pp. 119-121
Structure-activity relationship study of Asiatic acid derivatives against beta amyloid (A beta)-induced neurotoxicity (vol 10, pg 119, 2000)
Authors: Jew, SS Yoo, CH Lim, DY Kim, H Mook-Jung, I Jung, MW Choi, H Jung, YH Kim, H Park, HG
Citation: Ss. Jew et al., Structure-activity relationship study of Asiatic acid derivatives against beta amyloid (A beta)-induced neurotoxicity (vol 10, pg 119, 2000), BIOORG MED, 10(13), 2000, pp. 1495-1495
Enantioselective synthesis of (S)-N,N-diethyl-2-formyl-2-(methoxymethoxy)butyramide, a key intermediate for 20(S)-camptothecin analogues, via asymmetric bromolactonization
Authors: Jew, SS Roh, EY Kim, HJ Kim, MG Park, HG
Citation: Ss. Jew et al., Enantioselective synthesis of (S)-N,N-diethyl-2-formyl-2-(methoxymethoxy)butyramide, a key intermediate for 20(S)-camptothecin analogues, via asymmetric bromolactonization, TETRAHEDR-A, 11(19), 2000, pp. 3985-3994
Asymmetric synthesis of (R)-(+)-etomoxir via enzymatic resolution
Authors: Jew, SS Roh, EY Baek, EY Mireille, L Kim, HO Jeong, BS Park, MK Park, HG
Citation: Ss. Jew et al., Asymmetric synthesis of (R)-(+)-etomoxir via enzymatic resolution, TETRAHEDR-A, 11(16), 2000, pp. 3395-3401
Pharmacokinetics, skin absorption, stability, blood partition, and proteinbinding of AS 2-006A, a new wound healing agent
Authors: Kim, GB Kim, YG Kim, SH Park, HG Jew, SS Lee, MG
Citation: Gb. Kim et al., Pharmacokinetics, skin absorption, stability, blood partition, and proteinbinding of AS 2-006A, a new wound healing agent, BIOPHARM DR, 21(3), 2000, pp. 113-119
Practical regioselective synthetic method for (E)-enol ether
Authors: Park, HG Kim, DH Yoo, MS Park, MK Jew, SS
Citation: Hg. Park et al., Practical regioselective synthetic method for (E)-enol ether, TETRAHEDR L, 41(23), 2000, pp. 4579-4582
Practical synthesis of (S)-7-(2-isopropylamino)ethylcamptothecin hydrochloride, potent topoisomerase I inhibitor
Authors: Ahn, SK Choi, NS Jeong, BS Kim, KK Journ, DJ Kim, JK Lee, SJ Kim, JW Hong, CI Jew, SS
Citation: Sk. Ahn et al., Practical synthesis of (S)-7-(2-isopropylamino)ethylcamptothecin hydrochloride, potent topoisomerase I inhibitor, J HETERO CH, 37(5), 2000, pp. 1141-1144
Determination of a new asiatic acid derivative, AS 2-006A in rat plasma and urine, and human plsma by high-performance liquid chromatography
Authors: Kim, GB Kim, YG Jew, SS Lee, MG
Citation: Gb. Kim et al., Determination of a new asiatic acid derivative, AS 2-006A in rat plasma and urine, and human plsma by high-performance liquid chromatography, RES COM M P, 104(3), 1999, pp. 339-344
Synthesis and in vitro cytotoxicity of hexacyclic camptothecin analogues
Authors: Jew, SS Kim, HJ Kim, MG Roh, EE Hong, CI Kim, JK Lee, JH Lee, H Park, HG
Citation: Ss. Jew et al., Synthesis and in vitro cytotoxicity of hexacyclic camptothecin analogues, BIOORG MED, 9(22), 1999, pp. 3203-3206
Regioselective ring opening of steroidal epoxide with hydrides: Formation of C(2)- and C(3)-deoxyasiatic acid derivatives
Authors: Jew, SS Lim, D Seo, SK Nam, TG Park, HG Kim, HD Kim, CM Lee, MH Paik, HG Lee, MJ Jung, YH
Citation: Ss. Jew et al., Regioselective ring opening of steroidal epoxide with hydrides: Formation of C(2)- and C(3)-deoxyasiatic acid derivatives, ARCH PH RES, 21(6), 1998, pp. 793-795
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