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Results: 1-13 |
Results: 13

Authors: Hua, DH McGill, JW Robinson, PD Meyers, CY
Citation: Dh. Hua et al., 2,4,6-Tris(1 '-phenylthio-1-ferrocenyl)boroxin, ACT CRYST E, 57, 2001, pp. m413-m415

Authors: Meyers, CY Hua, DH Hou, YQ Robinson, PD
Citation: Cy. Meyers et al., 2-Chloro-2-propyl mesityl sulfone, ACT CRYST E, 57, 2001, pp. o587-o589

Authors: Wang, BN Wu, MF Perchellet, EM McIlvain, CJ Sperfslage, BJ Huang, XD Tamura, M Stephany, HA Hua, DH Perchellet, JP
Citation: Bn. Wang et al., A synthetic triptycene bisquinone, which blocks nucleoside transport and induces DNA fragmentation, retains its cytotoxic efficacy in daunorubicin-resistant HL-60 cell lines, INT J ONCOL, 19(6), 2001, pp. 1169-1178

Authors: Hua, DH Nguyen, TXC McGill, JW Chen, Y Robinson, PD
Citation: Dh. Hua et al., Resolution of 8 '-alkoxy- and hydroxy-1,1 '-binaphthalen-8-ols, TETRAHEDR-A, 12(14), 2001, pp. 1999-2004

Authors: Hua, DH McGill, JW Ueda, M Stephany, HA
Citation: Dh. Hua et al., Short syntheses of 8-substituted 8 '-[1-(1 '-phenylthio)ferrocenyl]-1,1 '-binaphthyls from Suzuki coupling reactions. A strategy for generating new chiral ligands and charge-transfer complexes, J ORGMET CH, 637, 2001, pp. 832-836

Authors: Perchellet, EM Magill, MJ Huang, XD Dalke, DM Hua, DH Perchellet, JP
Citation: Em. Perchellet et al., 1,4-Anthraquinone: an anticancer drug that blocks nucleoside transport, inhibits macromolecule synthesis, induces DNA fragmentation, and decreases the growth and viability of L1210 leukemic cells in the same nanomolar range as daunorubicin in vitro, ANTI-CANC D, 11(5), 2000, pp. 339-352

Authors: Robinson, PD Hua, DH Fan, JM Liu, LZ McGill, JW Arshid, M Meyers, CY
Citation: Pd. Robinson et al., cis,cis,cis-Tetramethyl 1,2,4,5-cyclohexanetetracarboxylate, ACT CRYST C, 56, 2000, pp. 1471-1472

Authors: Hua, DH Takasu, K Huang, XD Millward, GS Chen, Y Fan, JM
Citation: Dh. Hua et al., Palladium-mediated ring closure reactions. Facile syntheses of enantiopurebicyclic and tricyclic alkenones, TETRAHEDRON, 56(38), 2000, pp. 7389-7398

Authors: Perchellet, EM Magill, MJ Huang, XD Brantis, CE Hua, DH Perchellet, JP
Citation: Em. Perchellet et al., Triptycenes: a novel synthetic class of bifunctional anticancer drugs thatinhibit nucleoside transport, induce DNA cleavage and decrease the viability of leukemic cells in the nanomolar range in vitro, ANTI-CANC D, 10(8), 1999, pp. 749-766

Authors: Perchellet, EM Ladesich, JB Magill, MJ Chen, Y Hua, DH Perchellet, JP
Citation: Em. Perchellet et al., Tricyclic pyrone analogs: a new synthetic class of bifunctional anticancerdrugs that inhibit nucleoside transport, microtubule assembly, the viability of leukemic cells in vitro and the growth of solid tumors in vivo, ANTI-CANC D, 10(5), 1999, pp. 489-504

Authors: Xiao, H Zheng, XY Dong, XL Hua, DH Li, Q Luo, H Liu, JM Liu, W
Citation: H. Xiao et al., A research on the body center of mass of Chinese adults, INT J IND E, 23(1-2), 1999, pp. 129-133

Authors: Robinson, PD Beatty, A Hua, DH Chen, Y Meyers, CY Perchellet, EM Ladesich, JB Perchellet, JP
Citation: Pd. Robinson et al., Racemic 3-(3,4-dimethoxyphenyl)-5a,6,8,9-tetrahydro-1H,7H-pyrano[4,3-b][1]benzo-pryan-1-one, an active antitumor agent, ACT CRYST C, 55, 1999, pp. 1188-1190

Authors: Hua, DH Chen, Y Sin, HS Robinson, PD Meyers, CY Perchellet, EM Perchellet, JP Chiang, PK Biellmann, JF
Citation: Dh. Hua et al., 6,7,8,9-Tetrahydro-3-methyl-1H-pyrano[4,3-b]quinolin-1-one, ACT CRYST C, 55, 1999, pp. 1698-1701
Risultati: 1-13 |