Citation: Qm. Wang et al., A convenient synthesis of N-t-butyl-N '-aminocarbonyl-N-(substituted)benzoyl-hydrazine containing alpha-aminoalkylphosphonate groups in a one-pot procedure, HETEROAT CH, 12(2), 2001, pp. 68-72
Citation: Qm. Wang et al., Synthesis and biological activity of novel N-sulfenylated derivatives of diacylhydrazines, J CHEM R-S, (8), 2001, pp. 342-343
Authors:
Fang, YY
Wang, X
Li, HY
Ma, Y
Yuan, MX
Huang, RQ
Lai, CM
Citation: Yy. Fang et al., Using molecular graphics, molecular mechanics, quantum chemistry and electrostatic potential methods to study structure-property relationship on pesticides (XIII) - Studies on three-dimensional quantitative structure-activity relationship between the structures of O-(4-quinazolinyl)oxime ethers andtheir antiviral activity, CHEM J CH U, 22(4), 2001, pp. 587-590
Citation: Qm. Wang et Rq. Huang, Synthesis and biological activity of novel N '-tert-butyl-N '-substituted benzoyl-N-(substituted phenyl)aminocarbonylhydrazines and their derivatives, TETRAHEDR L, 42(50), 2001, pp. 8881-8883
Citation: Zg. Li et al., Isolation, total synthesis and biological activity of phenanthroindolizidine and phenanthroquinolizidine alkaloids, SYNTHESIS-S, (16), 2001, pp. 2365-2378
Authors:
Huang, RQ
Bell-Horner, CL
Dibas, MI
Covey, DF
Drewe, JA
Dillon, GH
Citation: Rq. Huang et al., Pentylenetetrazole-induced inhibition of recombinant gamma-aminobutyric acid type A (GABA(A)) receptors: Mechanism and site of action, J PHARM EXP, 298(3), 2001, pp. 986-995
Citation: Qm. Wang et Rq. Huang, Condensation reaction of 1-oxo-4-chlorocarbonyl-1-phospha-2,6,7-trioxabicyclo[2.2.2]octane with N-t-butyl-N-benzoylhydrazine, PHOSPHOR SU, 161, 2000, pp. 173-179
Citation: L. Zhang et al., Lipophilicity determination of N-(benzothiazol-2-yl)-alpha-amino alkyl phosphonic diesters by RP-HPLC and RP-HPTLC, CHIN J CHEM, 18(6), 2000, pp. 872-876
Authors:
Bell-Horner, CL
Dibas, M
Huang, RQ
Drewe, JA
Dillon, GH
Citation: Cl. Bell-horner et al., Influence of subunit configuration on the interaction of picrotoxin-site ligands with recombinant GABA(A) receptors, MOL BRAIN R, 76(1), 2000, pp. 47-55
Citation: Qm. Wang et Rq. Huang, A new and convenient synthesis of germatranes using molecular sieves (3 angstrom) as dehydrating agents, TETRAHEDR L, 41(17), 2000, pp. 3153-3155
Citation: Rq. Huang et Gh. Dillon, Direct inhibition of glycine receptors by genistein, a tyrosine kinase inhibitor, NEUROPHARM, 39(11), 2000, pp. 2195-2204
Citation: Qm. Wang et al., Synthesis and bioactivities of novel organogermanium sesquioxides containing alpha-aminophosphonate groups, HETEROAT CH, 10(3), 1999, pp. 209-212
Citation: Zg. Li et al., The synthesis of alpha-(4-antipyryl)amino-(substituted) phenyl-methylphosphonic acid derivatives, PHOSPHOR SU, 155, 1999, pp. 137-145
Citation: Zg. Li et al., Crystal structure of diethyl 1-(6-methyl-2-benzothiaylamino)-2,4-dichlorophenylmethylphosphonate, CHIN J ST C, 18(4), 1999, pp. 259-262
Citation: X. Liu et al., Synthesis and crystal structure of ethoxyethyl 3-(2-chloro-5-pyridyl methylamino)-2-cyano-3-methylthio acrylate, CHIN J ST C, 18(4), 1999, pp. 282-285
Authors:
Cheng, JR
Wen, J
Shao, RL
Cao, HY
Huang, RQ
Citation: Jr. Cheng et al., Synthesis and biological activity of diastereomeric racemates of asymmetric 1,3,2-benzodioxaphosphorin derivatives, CHEM J CH U, 20(9), 1999, pp. 1390-1393