-
1
-
-
0036265090
-
The epidemiology of epilepsy: The size of the problem
-
Bell, G. S.; Sander, J. W. The epidemiology of epilepsy: the size of the problem. Seizure 2002, 11 (Suppl. A), 306-314.
-
(2002)
Seizure
, vol.11
, Issue.SUPPL. A
, pp. 306-314
-
-
Bell, G.S.1
Sander, J.W.2
-
2
-
-
0343566431
-
The new drugs and strategies to manage epilepsy
-
Lopes Lima, J. M. The new drugs and strategies to manage epilepsy. Curr. Pharmac. Des. 2000, 6, 873-878.
-
(2000)
Curr. Pharmac. Des
, vol.6
, pp. 873-878
-
-
Lopes Lima, J.M.1
-
3
-
-
0036150267
-
Marketed new antiepileptic drugs: Are they better than old-generation agents?
-
Perucca, E. Marketed new antiepileptic drugs: are they better than old-generation agents? Ther. Drug Monit. 2002, 24, 74-80.
-
(2002)
Ther. Drug Monit
, vol.24
, pp. 74-80
-
-
Perucca, E.1
-
4
-
-
0034873696
-
Emerging options in the treatment of bipolar disorders
-
Berk, M.; Segal, J.; Janet, L.; Vorster, M. Emerging options in the treatment of bipolar disorders. Drugs 2001, 61, 1407-1414.
-
(2001)
Drugs
, vol.61
, pp. 1407-1414
-
-
Berk, M.1
Segal, J.2
Janet, L.3
Vorster, M.4
-
6
-
-
33847095107
-
Drug transporters in the epileptic brain
-
Löscher, W. Drug transporters in the epileptic brain. Epilepsia 2007, 48, 8-13.
-
(2007)
Epilepsia
, vol.48
, pp. 8-13
-
-
Löscher, W.1
-
7
-
-
34447312716
-
Idiosyncratic adverse reactions to antiepileptic drugs
-
Zaccara, G.; Franciotta, D.; Perucca, E. Idiosyncratic adverse reactions to antiepileptic drugs. Epilepsia 2007, 48, 1223-1244.
-
(2007)
Epilepsia
, vol.48
, pp. 1223-1244
-
-
Zaccara, G.1
Franciotta, D.2
Perucca, E.3
-
8
-
-
33846194013
-
-
Bialer, M.; Johannessen, S. I.; Kupferberg, H. J.; Levy, R. H.; Perucca, E.; Tomson, T. Progress report on new antiepileptic drugs: a summary of the Eighth Eilat Conference (EILAT VIII). Epilepsy Res. 2007, 73, 1-52.
-
Bialer, M.; Johannessen, S. I.; Kupferberg, H. J.; Levy, R. H.; Perucca, E.; Tomson, T. Progress report on new antiepileptic drugs: a summary of the Eighth Eilat Conference (EILAT VIII). Epilepsy Res. 2007, 73, 1-52.
-
-
-
-
9
-
-
33747049831
-
Diverse mechanisms of antiepileptic drugs in the development pipeline
-
Rogawski, M. A. Diverse mechanisms of antiepileptic drugs in the development pipeline. Epilepsy Res. 2006, 69, 273-294.
-
(2006)
Epilepsy Res
, vol.69
, pp. 273-294
-
-
Rogawski, M.A.1
-
10
-
-
26444438132
-
Discovery of N-(2,6-dimeth- ylphenyl)-substituted semicarbazones as anticonvulsants: Hybrid phar-macophore-based design
-
Yogeeswari, P.; Sriram, D.; Thirumurugan, R.; Raghavendran, J. V.; Sudhan, K.; Pavana, R. K.; Stables, J. Discovery of N-(2,6-dimeth- ylphenyl)-substituted semicarbazones as anticonvulsants: hybrid phar-macophore-based design. J. Med. Chem. 2005, 48, 6202-6211.
-
(2005)
J. Med. Chem
, vol.48
, pp. 6202-6211
-
-
Yogeeswari, P.1
Sriram, D.2
Thirumurugan, R.3
Raghavendran, J.V.4
Sudhan, K.5
Pavana, R.K.6
Stables, J.7
-
11
-
-
0347761409
-
Investigation into new anticonvulsant derivatives of α-substituted N-benzylamides of γ-hydroxy- and γ-acetoxybutyric acid. Part 5: Search for new anticonvulsant compounds
-
Malawska, B.; Kulig, K.; Spiewak, A.; Stables, J. P. Investigation into new anticonvulsant derivatives of α-substituted N-benzylamides of γ-hydroxy- and γ-acetoxybutyric acid. Part 5: Search for new anticonvulsant compounds. Bioorg. Med. Chem. 2004, 12, 625-632.
-
(2004)
Bioorg. Med. Chem
, vol.12
, pp. 625-632
-
-
Malawska, B.1
Kulig, K.2
Spiewak, A.3
Stables, J.P.4
-
12
-
-
2942701907
-
Characterization of the anticonvulsant profile of valpromide derivatives
-
Tasso, S. M.; Moon, S. C.; Bruno-Blanch, L. E.; Estiú, G. L. Characterization of the anticonvulsant profile of valpromide derivatives. Bioorg. Med. Chem. 2004, 12, 3857-3869.
-
(2004)
Bioorg. Med. Chem
, vol.12
, pp. 3857-3869
-
-
Tasso, S.M.1
Moon, S.C.2
Bruno-Blanch, L.E.3
Estiú, G.L.4
-
13
-
-
30344485440
-
QSAR of the anticonvulsant enaminones; molecular modeling aspects and other assessments
-
Wilson, T. L.; Jackson, P. L.; Hanson, C. D.; Xue, Z.; Eddington, N. D.; Scott, K. R. QSAR of the anticonvulsant enaminones; molecular modeling aspects and other assessments. Med. Chem. 2005, 1, 371-381.
-
(2005)
Med. Chem
, vol.1
, pp. 371-381
-
-
Wilson, T.L.1
Jackson, P.L.2
Hanson, C.D.3
Xue, Z.4
Eddington, N.D.5
Scott, K.R.6
-
14
-
-
0034640722
-
Pharmacophore searching and QSAR analysis in the design of anticonvulsant drugs
-
Tasso, S. M.; Bruno-Blanch, L. E.; Moon, S. C.; Estiu, G. L. Pharmacophore searching and QSAR analysis in the design of anticonvulsant drugs. J. Mol. Struct. (THEOCHEM) 2000, 504, 229-240.
-
(2000)
J. Mol. Struct. (THEOCHEM)
, vol.504
, pp. 229-240
-
-
Tasso, S.M.1
Bruno-Blanch, L.E.2
Moon, S.C.3
Estiu, G.L.4
-
15
-
-
33846875238
-
A pharmacophore derived phenytoin analogue with increased affinity for slow inactivated sodium channels exhibits a desired anticonvulsant profile
-
Lenkowski, P. W.; Batts, T. W.; Smith, M. D.; Ko, S.-H.; Jones, P. J.; Taylor, C. H.; McCusker, A. K.; Davis, G. C.; Hartmann, H. A.; White, H. S.; Brown, M. L.; Patel, M. K. A pharmacophore derived phenytoin analogue with increased affinity for slow inactivated sodium channels exhibits a desired anticonvulsant profile. Neuropharmacology 2007, 52, 1044-1054.
-
(2007)
Neuropharmacology
, vol.52
, pp. 1044-1054
-
-
Lenkowski, P.W.1
Batts, T.W.2
Smith, M.D.3
Ko, S.-H.4
Jones, P.J.5
Taylor, C.H.6
McCusker, A.K.7
Davis, G.C.8
Hartmann, H.A.9
White, H.S.10
Brown, M.L.11
Patel, M.K.12
-
16
-
-
33845943300
-
3D-QSAR design of novel antiepileptic sulfamides
-
Gavernet, L.; Dominguez Cabrera, M. J.; Bruno-Blanch, L. E.; Estiú, G. L. 3D-QSAR design of novel antiepileptic sulfamides. Bioorg. Med. Chem. 2007, 15, 1556-1567.
-
(2007)
Bioorg. Med. Chem
, vol.15
, pp. 1556-1567
-
-
Gavernet, L.1
Dominguez Cabrera, M.J.2
Bruno-Blanch, L.E.3
Estiú, G.L.4
-
17
-
-
34250725563
-
Design, synthesis, and anticonvulsant activity of some sulfamides
-
Gavernet, L.; Barrios, I. A.; Sella Cravero, M.; Bruno-Blanch, L. E. Design, synthesis, and anticonvulsant activity of some sulfamides. Bioorg. Med. Chem. 2007, 15, 5604-5614.
-
(2007)
Bioorg. Med. Chem
, vol.15
, pp. 5604-5614
-
-
Gavernet, L.1
Barrios, I.A.2
Sella Cravero, M.3
Bruno-Blanch, L.E.4
-
18
-
-
3042798891
-
The neurobiology of antiepileptic drugs
-
Rogawski, M. A.; Löscher, W. The neurobiology of antiepileptic drugs. Nat. Rev. Neurosci. 2004, 5, 553-564.
-
(2004)
Nat. Rev. Neurosci
, vol.5
, pp. 553-564
-
-
Rogawski, M.A.1
Löscher, W.2
-
19
-
-
0027256538
-
The design of a dipeptide library for screening at peptide receptor sites
-
Horwell, D. C.; Howson, W.; Ratcliffe, G. S.; Rees, D. C. The design of a dipeptide library for screening at peptide receptor sites. Bioorg. Med. Chem. Lett. 1993, 3, 799-802.
-
(1993)
Bioorg. Med. Chem. Lett
, vol.3
, pp. 799-802
-
-
Horwell, D.C.1
Howson, W.2
Ratcliffe, G.S.3
Rees, D.C.4
-
20
-
-
0038820017
-
Synthesis and Anticonvulsant Activity of Novel Bicyclic Acidic Amino Acids
-
Conti, P.; De Amici, M.; di Ventimiglia, S. J.; Stensbøl, T. B.; Madsen, U.; Braüner-Osborne, H.; Russo, E.; De Sarro, G.; Bruno, G.; De Micheli, C. Synthesis and Anticonvulsant Activity of Novel Bicyclic Acidic Amino Acids. J. Med. Chem. 2003, 46, 3102-3108.
-
(2003)
J. Med. Chem
, vol.46
, pp. 3102-3108
-
-
Conti, P.1
De Amici, M.2
di Ventimiglia, S.J.3
Stensbøl, T.B.4
Madsen, U.5
Braüner-Osborne, H.6
Russo, E.7
De Sarro, G.8
Bruno, G.9
De Micheli, C.10
-
21
-
-
34249082410
-
Discovery of 4-Aminobu-tyric Acid Derivatives Possessing Anticonvulsant and Antinociceptive Activities: A Hybrid Pharmacophore Approach
-
Yogeeswari, P.; Ragavendran, J. V.; Sriram, D.; Nageswari, Y.; Kavya, R.; Sreevatsan, N.; Vanitha, K.; Stables, J. Discovery of 4-Aminobu-tyric Acid Derivatives Possessing Anticonvulsant and Antinociceptive Activities: A Hybrid Pharmacophore Approach. J. Med. Chem. 2007, 50, 2459-2467.
-
(2007)
J. Med. Chem
, vol.50
, pp. 2459-2467
-
-
Yogeeswari, P.1
Ragavendran, J.V.2
Sriram, D.3
Nageswari, Y.4
Kavya, R.5
Sreevatsan, N.6
Vanitha, K.7
Stables, J.8
-
22
-
-
17344380190
-
The de novo design and synthesis of cyclic urea inhibitors of factor Xa: Optimization of the S4 ligand
-
Galemmo, R. A., Jr.; Wells, B. L.; Rossi, K. A.; Alexander, R. S.; Dominguez, C.; Maduskuie, T. P.; Stouten, P. F. W.; Wright, M. R.; Aungst, B. J.; Wong, P. C.; Knabb, R. M.; Wexler, R. R. The de novo design and synthesis of cyclic urea inhibitors of factor Xa: optimization of the S4 ligand. Bioorg. Med. Chem. Lett. 2000, 10, 301-304.
-
(2000)
Bioorg. Med. Chem. Lett
, vol.10
, pp. 301-304
-
-
Galemmo Jr., R.A.1
Wells, B.L.2
Rossi, K.A.3
Alexander, R.S.4
Dominguez, C.5
Maduskuie, T.P.6
Stouten, P.F.W.7
Wright, M.R.8
Aungst, B.J.9
Wong, P.C.10
Knabb, R.M.11
Wexler, R.R.12
-
23
-
-
15644373221
-
Nonsymmetric P2/ P2′ Cyclic Urea HIV Protease Inhibitors. Structure-Activity Relationship, Bioavailability, and Resistance Profile of Monoindazole-Substituted P2 Analogues
-
De Lucca, G. V.; Kim, U. T.; Liang, J.; Cordova, B.; Klabe, R. M.; Garber, S.; Bacheler, L. T.; Lam, G. N.; Wright, M. R.; Logue, K. A.; Erickson-Viitanen, S.; Ko, S. S.; Trainor, G. L. Nonsymmetric P2/ P2′ Cyclic Urea HIV Protease Inhibitors. Structure-Activity Relationship, Bioavailability, and Resistance Profile of Monoindazole-Substituted P2 Analogues. J. Med. Chem. 1998, 41, 2411-2423.
-
(1998)
J. Med. Chem
, vol.41
, pp. 2411-2423
-
-
De Lucca, G.V.1
Kim, U.T.2
Liang, J.3
Cordova, B.4
Klabe, R.M.5
Garber, S.6
Bacheler, L.T.7
Lam, G.N.8
Wright, M.R.9
Logue, K.A.10
Erickson-Viitanen, S.11
Ko, S.S.12
Trainor, G.L.13
-
24
-
-
0032550655
-
Calculated and Experimental Low-Energy Conformations of Cyclic Urea HIV Protease Inhibitors
-
Hodge, C. N.; Lam, P. Y. S.; Eyermann, C. J.; Jadhav, P. K.; Ru, Y.; Fernandez, C. H.; De Lucca, G. V.; Chang, C.-H.; Kaltenbach, R. F., III.; Holler, E. R.; Woerner, F.; Daneker, W. F.; Emmett, G.; Calabrese, J. C.; Aldrich, P. E. Calculated and Experimental Low-Energy Conformations of Cyclic Urea HIV Protease Inhibitors. J. Am. Chem. Soc. 1998, 120, 4570-4581.
-
(1998)
J. Am. Chem. Soc
, vol.120
, pp. 4570-4581
-
-
Hodge, C.N.1
Lam, P.Y.S.2
Eyermann, C.J.3
Jadhav, P.K.4
Ru, Y.5
Fernandez, C.H.6
De Lucca, G.V.7
Chang, C.-H.8
Kaltenbach III, R.F.9
Holler, E.R.10
Woerner, F.11
Daneker, W.F.12
Emmett, G.13
Calabrese, J.C.14
Aldrich, P.E.15
-
25
-
-
0028057975
-
Nonpeptide cyclic ureas as HIV protease inhibitors
-
Lam, P. Y. S.; Jadhav, P. K.; Eyermann, C. J.; Hodge, C. N.; Ru, Y.; Bachelor, L. T.; Meek, J. L.; Otto, M. J.; Rayner, M. M.; Wong, Y. N.; Chang, C.-H.; Weber, P. C. Nonpeptide cyclic ureas as HIV protease inhibitors. Science 1994, 263, 380-384.
-
(1994)
Science
, vol.263
, pp. 380-384
-
-
Lam, P.Y.S.1
Jadhav, P.K.2
Eyermann, C.J.3
Hodge, C.N.4
Ru, Y.5
Bachelor, L.T.6
Meek, J.L.7
Otto, M.J.8
Rayner, M.M.9
Wong, Y.N.10
Chang, C.-H.11
Weber, P.C.12
-
26
-
-
0034624208
-
Ring-Closing Metathesis Strategies to Cyclic Sulfamide Peptidomimetics
-
Dougherty, J. M.; Probs, D. A.; Robinson, R. E.; Moore, J. D.; Klein, T. A.; Snelgrove, K. A.; Hanson, P. R. Ring-Closing Metathesis Strategies to Cyclic Sulfamide Peptidomimetics. Tetrahedron 2000, 56, 9781-9790.
-
(2000)
Tetrahedron
, vol.56
, pp. 9781-9790
-
-
Dougherty, J.M.1
Probs, D.A.2
Robinson, R.E.3
Moore, J.D.4
Klein, T.A.5
Snelgrove, K.A.6
Hanson, P.R.7
-
27
-
-
0030993410
-
Structure-Based Design of a General Class of Mechanism-Based Inhibitors of the Serine Proteinases Employing a Novel Amino Acid-Derived Heterocyclic Scaffold
-
Groutas, W. C.; Kuang, R.; Venkataraman, R.; Epp, J. B.; Ruan, S.; Prakash, O. Structure-Based Design of a General Class of Mechanism-Based Inhibitors of the Serine Proteinases Employing a Novel Amino Acid-Derived Heterocyclic Scaffold. Biochemistry 1997, 36, 4739-4750.
-
(1997)
Biochemistry
, vol.36
, pp. 4739-4750
-
-
Groutas, W.C.1
Kuang, R.2
Venkataraman, R.3
Epp, J.B.4
Ruan, S.5
Prakash, O.6
-
28
-
-
0033536494
-
A General Inhibitor Scaffold for Serine Proteases with a (Chymo)trypsin-Like Fold: Solution-Phase Construction and Evaluation of the First Series of Libraries of Mechanism- Based Inhibitors
-
Kuang, R.; Epp, J. B.; Ruan, S.; Yu, H.; Huang, P.; He, S.; Tu, J.; Schechter, N. M.; Turbov, J.; Froelich, C. J.; Groutas, W. C. A General Inhibitor Scaffold for Serine Proteases with a (Chymo)trypsin-Like Fold: Solution-Phase Construction and Evaluation of the First Series of Libraries of Mechanism- Based Inhibitors. J. Am. Chem. Soc. 1999, 121, 8128-8129.
-
(1999)
J. Am. Chem. Soc
, vol.121
, pp. 8128-8129
-
-
Kuang, R.1
Epp, J.B.2
Ruan, S.3
Yu, H.4
Huang, P.5
He, S.6
Tu, J.7
Schechter, N.M.8
Turbov, J.9
Froelich, C.J.10
Groutas, W.C.11
-
29
-
-
0031835168
-
Potent and Specific Inhibition of Human Leukocyte Elastase, Cathepsin G and Proteinase 3 by Sulfone Derivatives Employing the 1,2,5-Thiadiazolidin-3-one 1,1 Dioxide Scaffold
-
Groutas, W. C.; Kuang, R.; Ruan, S.; Epp, J. B.; Venkataraman, R.; Truong, T. M. Potent and Specific Inhibition of Human Leukocyte Elastase, Cathepsin G and Proteinase 3 by Sulfone Derivatives Employing the 1,2,5-Thiadiazolidin-3-one 1,1 Dioxide Scaffold. Bioorg. Med. Chem. 1998, 6, 661-671.
-
(1998)
Bioorg. Med. Chem
, vol.6
, pp. 661-671
-
-
Groutas, W.C.1
Kuang, R.2
Ruan, S.3
Epp, J.B.4
Venkataraman, R.5
Truong, T.M.6
-
30
-
-
0032848551
-
Sulfahydantoins as Tripeptide Constraints: Synthesis and Structure of Chiral Substituted 3-oxo-1,2,5-thiadiazolidine 1,1-dioxides
-
Boudjabi, S.; Dewynter, G.; Voyer, N.; Toupet, L.; Montero, J.-L. Sulfahydantoins as Tripeptide Constraints: Synthesis and Structure of Chiral Substituted 3-oxo-1,2,5-thiadiazolidine 1,1-dioxides. Eur. J. Org. Chem. 1999, 9, 2275-2283.
-
(1999)
Eur. J. Org. Chem
, vol.9
, pp. 2275-2283
-
-
Boudjabi, S.1
Dewynter, G.2
Voyer, N.3
Toupet, L.4
Montero, J.-L.5
-
31
-
-
37049031057
-
Potent Anticonvulsant Urea Derivatives of Constitutional Isomers of Valproic Acid
-
Shimshoni, J. A.; Bialer, M.; Wlodarczyk, B.; Finnell, R. H.; Yagen, B. Potent Anticonvulsant Urea Derivatives of Constitutional Isomers of Valproic Acid. J. Med. Chem. 2007, 50, 6419-6427.
-
(2007)
J. Med. Chem
, vol.50
, pp. 6419-6427
-
-
Shimshoni, J.A.1
Bialer, M.2
Wlodarczyk, B.3
Finnell, R.H.4
Yagen, B.5
-
32
-
-
3543031633
-
New generation of valproic acid
-
Trojnar, M. K.; Wierzchowska-Cioch, E.; Krzyzanowski, M.; Jargiello, M.; Czuczwar, S. J. New generation of valproic acid. Pol. J. Phar-macol. 2004, 56, 283-288.
-
(2004)
Pol. J. Phar-macol
, vol.56
, pp. 283-288
-
-
Trojnar, M.K.1
Wierzchowska-Cioch, E.2
Krzyzanowski, M.3
Jargiello, M.4
Czuczwar, S.J.5
-
33
-
-
0029020746
-
Pharmacokinetic Analysis and Antiepileptic Activity of N-Valproyl Derivatives of GABA and Glycine
-
Hadad, S.; Bialer, M. Pharmacokinetic Analysis and Antiepileptic Activity of N-Valproyl Derivatives of GABA and Glycine. Pharm. Res. 1995, 12, 905-910.
-
(1995)
Pharm. Res
, vol.12
, pp. 905-910
-
-
Hadad, S.1
Bialer, M.2
-
34
-
-
0030819103
-
Pharmacokinetic Analysis and Antiepileptic Activity of Two New Isomers of N-Valproyl Glycinamide
-
Hadad, S.; Bialer, M. Pharmacokinetic Analysis and Antiepileptic Activity of Two New Isomers of N-Valproyl Glycinamide. Biopharm. Drug Dispos. 1997, 18, 557-566.
-
(1997)
Biopharm. Drug Dispos
, vol.18
, pp. 557-566
-
-
Hadad, S.1
Bialer, M.2
-
35
-
-
0034844676
-
Anticon-vulsant Profile of Valrocemide (TV1901): A New Antiepileptic Drug
-
Isoherranen, N.; Woodhead, H. J.; White, H. S.; Bialer, M. Anticon-vulsant Profile of Valrocemide (TV1901): A New Antiepileptic Drug. Epilepsia 2001, 42, 831-836.
-
(2001)
Epilepsia
, vol.42
, pp. 831-836
-
-
Isoherranen, N.1
Woodhead, H.J.2
White, H.S.3
Bialer, M.4
-
36
-
-
0034624208
-
Ring-Closing Metathesis Strategies to Cyclic Sulfamide Peptidomimetics
-
Dougherty, J. M.; Probst, D. A.; Robinson, R. E.; Moore, J. D.; Klein, T. A.; Snelgrove, K. A.; Hanson, P. R. Ring-Closing Metathesis Strategies to Cyclic Sulfamide Peptidomimetics. Tetrahedron 2000, 56, 9781-9790.
-
(2000)
Tetrahedron
, vol.56
, pp. 9781-9790
-
-
Dougherty, J.M.1
Probst, D.A.2
Robinson, R.E.3
Moore, J.D.4
Klein, T.A.5
Snelgrove, K.A.6
Hanson, P.R.7
-
37
-
-
0030040762
-
Synthesis of pseudonucleosides containing chiral sulfahydantoins as aglycone (II)
-
Dewynter, G.; Aouf, N.; Regainia, Z.; Montero, J.-L. Synthesis of pseudonucleosides containing chiral sulfahydantoins as aglycone (II). Tetrahedron 1996, 52, 993-1004.
-
(1996)
Tetrahedron
, vol.52
, pp. 993-1004
-
-
Dewynter, G.1
Aouf, N.2
Regainia, Z.3
Montero, J.-L.4
-
38
-
-
0027391382
-
Synthèse de "sulfahydatoi'nes" chirales. Aspects stéréochimiques et protection régiospécifique.
-
Dewynter, G.; Aouf, N.; Criton, M.; Montero, J.-L. Synthèse de "sulfahydatoi'nes" chirales. Aspects stéréochimiques et protection régiospécifique. Tetrahedron 1993, 49, 65-76.
-
(1993)
Tetrahedron
, vol.49
, pp. 65-76
-
-
Dewynter, G.1
Aouf, N.2
Criton, M.3
Montero, J.-L.4
-
39
-
-
85077634689
-
The Use of Diethyl Azodicarboxylate and Triph-enylphosphine in Synthesis and Transformation of Natural Products
-
Mitsunobu, O. The Use of Diethyl Azodicarboxylate and Triph-enylphosphine in Synthesis and Transformation of Natural Products. Synthesis 1981, 1-28.
-
(1981)
Synthesis
, pp. 1-28
-
-
Mitsunobu, O.1
-
40
-
-
0019209905
-
Sulfonylamine-mediated sulfamation of amines. A mild, high yield synthesis of sulfamic acid salts
-
DuBois, G. E.; Stephenson, R. A. Sulfonylamine-mediated sulfamation of amines. A mild, high yield synthesis of sulfamic acid salts. J. Org. Chem. 1980, 45, 5371-5373.
-
(1980)
J. Org. Chem
, vol.45
, pp. 5371-5373
-
-
DuBois, G.E.1
Stephenson, R.A.2
-
41
-
-
0000692753
-
Amination of aryl sulfamate esters. A convenient general synthesis of aliphatic sulfamides
-
DuBois, G. E. Amination of aryl sulfamate esters. A convenient general synthesis of aliphatic sulfamides. J. Org. Chem. 1980, 45 (26), 5373-5375.
-
(1980)
J. Org. Chem
, vol.45
, Issue.26
, pp. 5373-5375
-
-
DuBois, G.E.1
-
42
-
-
0000821676
-
Structure and Size of the Non-Metallic Hydrides
-
Grimm, H. G. Structure and Size of the Non-Metallic Hydrides. Z. Electrochem. 1925, 31, 474-480.
-
(1925)
Z. Electrochem
, vol.31
, pp. 474-480
-
-
Grimm, H.G.1
-
43
-
-
34250969168
-
On the Systematic Arrangement of Chemical Compounds from the Perspective of Research on Atomic Composition and on Some Challenges in Experimental Chemistry
-
Grimm, H. G. On the Systematic Arrangement of Chemical Compounds from the Perspective of Research on Atomic Composition and on Some Challenges in Experimental Chemistry. Z. Naturwiss. 1929, 17, 557-564.
-
(1929)
Z. Naturwiss
, vol.17
, pp. 557-564
-
-
Grimm, H.G.1
-
44
-
-
0347761409
-
Investigation into new anticonvulsant derivatives of α-substituted N-benzylamides of γ-hydroxy- and γ-acetoxybutyric acid. Part 5: Search for new anticonvulsant compounds
-
Malawska, B.; Kulig, K.; Spiewak, A.; Stables, J. P. Investigation into new anticonvulsant derivatives of α-substituted N-benzylamides of γ-hydroxy- and γ-acetoxybutyric acid. Part 5: Search for new anticonvulsant compounds. Bioorg. Med. Chem. 2004, 12, 625-632.
-
(2004)
Bioorg. Med. Chem
, vol.12
, pp. 625-632
-
-
Malawska, B.1
Kulig, K.2
Spiewak, A.3
Stables, J.P.4
-
45
-
-
0021611548
-
Antiepileptic Drug Development Program
-
Porter, M.; Cereghino, M.; Gladding, R.; Hessie, B.; Kupferberg, D.; Scoville, M.; White, D. Antiepileptic Drug Development Program. Cleveland Clin. Q. 1984, 51, 293-305.
-
(1984)
Cleveland Clin. Q
, vol.51
, pp. 293-305
-
-
Porter, M.1
Cereghino, M.2
Gladding, R.3
Hessie, B.4
Kupferberg, D.5
Scoville, M.6
White, D.7
-
46
-
-
84951384024
-
A simplified method of evaluating dose- effect experiments
-
Litchfield, J. T.; Wilcoxon, F. A simplified method of evaluating dose- effect experiments. J. Pharmacol. Exp. Ther. 1949, 96, 99-113.
-
(1949)
J. Pharmacol. Exp. Ther
, vol.96
, pp. 99-113
-
-
Litchfield, J.T.1
Wilcoxon, F.2
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