-
1
-
-
0032878499
-
A compartmentalized model for the estimation of the cost of coccidiosis to the world's chicken production industry
-
Williams R.B. A compartmentalized model for the estimation of the cost of coccidiosis to the world's chicken production industry. Int. J. Parasitol. 29 (1999) 1209
-
(1999)
Int. J. Parasitol.
, vol.29
, pp. 1209
-
-
Williams, R.B.1
-
2
-
-
0036616356
-
Toxoplasma gondii cyclic GMP-dependent kinase: chemotherapeutic targeting of an essential parasite protein kinase
-
Donald R.G.K., Allocco J., Singh S.B., Nare B., Salowe S.P., Wiltsie J., and Liberator P.A. Toxoplasma gondii cyclic GMP-dependent kinase: chemotherapeutic targeting of an essential parasite protein kinase. Eukaryot. Cell 1 (2002) 317
-
(2002)
Eukaryot. Cell
, vol.1
, pp. 317
-
-
Donald, R.G.K.1
Allocco, J.2
Singh, S.B.3
Nare, B.4
Salowe, S.P.5
Wiltsie, J.6
Liberator, P.A.7
-
3
-
-
0037013273
-
Purification and molecular characterization of cGMP-dependent protein kinase from apicomplexan parasites: a novel chemotherapeutic target
-
Gurnett A.M., Liberator P.A., Dulski P.M., Salowe S.P., Donald R.G.K., Anderson J.W., Wiltsie J., Diaz C.A., Harris G., Chang B., Darkin-Rattray S.J., Nare B., Crumley T., Blum P.S., Misura A.S., Tamas T., Sardana M.K., Yuan J., Biftu T., and Schmatz D.M. Purification and molecular characterization of cGMP-dependent protein kinase from apicomplexan parasites: a novel chemotherapeutic target. J. Biol. Chem. 277 (2002) 15913
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 15913
-
-
Gurnett, A.M.1
Liberator, P.A.2
Dulski, P.M.3
Salowe, S.P.4
Donald, R.G.K.5
Anderson, J.W.6
Wiltsie, J.7
Diaz, C.A.8
Harris, G.9
Chang, B.10
Darkin-Rattray, S.J.11
Nare, B.12
Crumley, T.13
Blum, P.S.14
Misura, A.S.15
Tamas, T.16
Sardana, M.K.17
Yuan, J.18
Biftu, T.19
Schmatz, D.M.20
more..
-
4
-
-
33644986999
-
Synthesis and SAR studies of very potent imidazopyridine antiprotozoal agents
-
Biftu T., Feng D., Fisher M., Liang G.-B., Qian X., Scribner A., Dennis R., Lee S., Liberator P.A., Brown C., Gurnett A., Leavitt P.S., Thompson D., Mathew J., Misura A., Samaras S., Tamas T., Sina J.F., McNulty K.A., McKnight C.G., Schmatz D.M., and Wyvratt M. Synthesis and SAR studies of very potent imidazopyridine antiprotozoal agents. Bioorg. Med. Chem. Lett. 16 (2006) 2479
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 2479
-
-
Biftu, T.1
Feng, D.2
Fisher, M.3
Liang, G.-B.4
Qian, X.5
Scribner, A.6
Dennis, R.7
Lee, S.8
Liberator, P.A.9
Brown, C.10
Gurnett, A.11
Leavitt, P.S.12
Thompson, D.13
Mathew, J.14
Misura, A.15
Samaras, S.16
Tamas, T.17
Sina, J.F.18
McNulty, K.A.19
McKnight, C.G.20
Schmatz, D.M.21
Wyvratt, M.22
more..
-
5
-
-
33750528715
-
Synthesis and SAR of 2-(4-fluorophenyl)-3-pyrimidin-4-ylimidazo[1,2-a]pyridine derivatives as anticoccidial agents
-
Feng D., Fisher M., Liang G.-B., Qian X., Brown C., Gurnett A., Leavitt P.S., Liberator P.A., Mathew J., Misura A., Samaras S., Tamas T., Schmatz D.M., Wyvratt M., and Biftu T. Synthesis and SAR of 2-(4-fluorophenyl)-3-pyrimidin-4-ylimidazo[1,2-a]pyridine derivatives as anticoccidial agents. Bioorg. Med. Chem. Lett. 16 (2006) 5978
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 5978
-
-
Feng, D.1
Fisher, M.2
Liang, G.-B.3
Qian, X.4
Brown, C.5
Gurnett, A.6
Leavitt, P.S.7
Liberator, P.A.8
Mathew, J.9
Misura, A.10
Samaras, S.11
Tamas, T.12
Schmatz, D.M.13
Wyvratt, M.14
Biftu, T.15
-
6
-
-
36248942567
-
Synthesis and biological activity of imidazopyridine anticoccidial agents: part I, Eur
-
Scribner A., Dennis R., Hong J., Lee S., McIntyre D., Perrey D., Feng D., Fisher M., Wyvratt M., Leavitt P., Liberator P., Gurnett A., Brown C., Mathew J., Thompson D., Schmatz D., and Biftu T. Synthesis and biological activity of imidazopyridine anticoccidial agents: part I, Eur. J. Med. Chem. 42 11-12 (2007) 1334
-
(2007)
J. Med. Chem.
, vol.42
, Issue.11-12
, pp. 1334
-
-
Scribner, A.1
Dennis, R.2
Hong, J.3
Lee, S.4
McIntyre, D.5
Perrey, D.6
Feng, D.7
Fisher, M.8
Wyvratt, M.9
Leavitt, P.10
Liberator, P.11
Gurnett, A.12
Brown, C.13
Mathew, J.14
Thompson, D.15
Schmatz, D.16
Biftu, T.17
-
7
-
-
0035943317
-
Synthesis, characterization, and optical response of dipolar and non-dipolar poly(phenylenevinylene) dendrimers
-
Diez-Barra E., Garcia-Martinez J.C., Merino S., del Ray R., Rodriguez-Lopez J., Sanchez-Verdu P., and Tejeda J. Synthesis, characterization, and optical response of dipolar and non-dipolar poly(phenylenevinylene) dendrimers. J. Org. Chem. 66 (2001) 5664
-
(2001)
J. Org. Chem.
, vol.66
, pp. 5664
-
-
Diez-Barra, E.1
Garcia-Martinez, J.C.2
Merino, S.3
del Ray, R.4
Rodriguez-Lopez, J.5
Sanchez-Verdu, P.6
Tejeda, J.7
-
8
-
-
0000844109
-
Reductive amination of aldehydes and ketones with sodium triacetoxyborohydride. Studies on direct and indirect reductive amination procedures
-
Abdel-Magid A.F., Carson K.G., Harris B.D., Maryanoff C.A., and Shah R.D. Reductive amination of aldehydes and ketones with sodium triacetoxyborohydride. Studies on direct and indirect reductive amination procedures. J. Org. Chem. 61 (1996) 3849
-
(1996)
J. Org. Chem.
, vol.61
, pp. 3849
-
-
Abdel-Magid, A.F.1
Carson, K.G.2
Harris, B.D.3
Maryanoff, C.A.4
Shah, R.D.5
-
9
-
-
0035039374
-
Pyridazines part XXIII: efficient arylation at position 5 of the 6-phenyl-(2H)-pyridazin-3-one system using a Suzuki cross-coupling reaction
-
Coelho A., Sotelo E., Estevez I., and Ravina E. Pyridazines part XXIII: efficient arylation at position 5 of the 6-phenyl-(2H)-pyridazin-3-one system using a Suzuki cross-coupling reaction. Synthesis (2001) 871
-
(2001)
Synthesis
, pp. 871
-
-
Coelho, A.1
Sotelo, E.2
Estevez, I.3
Ravina, E.4
-
10
-
-
0001219906
-
A simple method for converting nitriles to amides. Hydrolysis with potassium hydroxide in tert-butyl alcohol
-
Hall J.H., and Gisler M. A simple method for converting nitriles to amides. Hydrolysis with potassium hydroxide in tert-butyl alcohol. J. Org. Chem. 41 (1976) 3769
-
(1976)
J. Org. Chem.
, vol.41
, pp. 3769
-
-
Hall, J.H.1
Gisler, M.2
-
11
-
-
0033620012
-
Synthesis, characterization, and structure-activity relationships of amidine-substituted (bis)benzylidine-cycloketone olefin isomers as potent and selective factor Xa inhibitors
-
Guilford W.J., Shaw K.J., Dallas J.L., Koovakkat S., Lee W., Liang A., Light D.R., McCarrick M.A., Whitlow M., Ye B., and Morrissey M.M. Synthesis, characterization, and structure-activity relationships of amidine-substituted (bis)benzylidine-cycloketone olefin isomers as potent and selective factor Xa inhibitors. J. Med. Chem. 42 (1999) 5415
-
(1999)
J. Med. Chem.
, vol.42
, pp. 5415
-
-
Guilford, W.J.1
Shaw, K.J.2
Dallas, J.L.3
Koovakkat, S.4
Lee, W.5
Liang, A.6
Light, D.R.7
McCarrick, M.A.8
Whitlow, M.9
Ye, B.10
Morrissey, M.M.11
-
12
-
-
0037472796
-
Hybrid-designed inhibitors of p38 MAP kinase utilizing N-arylpyridazinones
-
Colletti S.L., Frie J.L., Dixon E.C., Singh S.B., Choi B.K., Scapin G., Fitzgerald C.E., Kumar S., Nichols E.A., O'Keefe S.J., O'Neill E.A., Porter G., Samuel K., Schmatz D.M., Schwartz C.D., Shoop W.L., Thompson C.M., Thompson J.E., Wang R., Woods A., Zaller D.M., and Doherty J.B. Hybrid-designed inhibitors of p38 MAP kinase utilizing N-arylpyridazinones. J. Med. Chem. 46 (2003) 349
-
(2003)
J. Med. Chem.
, vol.46
, pp. 349
-
-
Colletti, S.L.1
Frie, J.L.2
Dixon, E.C.3
Singh, S.B.4
Choi, B.K.5
Scapin, G.6
Fitzgerald, C.E.7
Kumar, S.8
Nichols, E.A.9
O'Keefe, S.J.10
O'Neill, E.A.11
Porter, G.12
Samuel, K.13
Schmatz, D.M.14
Schwartz, C.D.15
Shoop, W.L.16
Thompson, C.M.17
Thompson, J.E.18
Wang, R.19
Woods, A.20
Zaller, D.M.21
Doherty, J.B.22
more..
-
13
-
-
0029084414
-
A new general method for preparation of N-methoxy-N-methylamides. Application in direct conversion of an ester to a ketone
-
Williams J.M., Jobson R.B., Yasunda N., Marchesini G., Dolling U.-H., and Grabowski E.J.J. A new general method for preparation of N-methoxy-N-methylamides. Application in direct conversion of an ester to a ketone. Tetrahedron Lett. 36 (1995) 5461
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 5461
-
-
Williams, J.M.1
Jobson, R.B.2
Yasunda, N.3
Marchesini, G.4
Dolling, U.-H.5
Grabowski, E.J.J.6
-
14
-
-
0020610190
-
Synthesis and biological evaluation of 2-fluoro-8-azaadenosine and related compounds
-
Montgomery J.A., Shortnacy A.T., and Secrist III J.A. Synthesis and biological evaluation of 2-fluoro-8-azaadenosine and related compounds. J. Med. Chem. 26 (1983) 1483
-
(1983)
J. Med. Chem.
, vol.26
, pp. 1483
-
-
Montgomery, J.A.1
Shortnacy, A.T.2
Secrist III, J.A.3
-
15
-
-
0025133334
-
A new mode of reactivity of N-methoxy-N-methylamides with strongly basic reagents
-
Graham S.L., and Scholz T.H. A new mode of reactivity of N-methoxy-N-methylamides with strongly basic reagents. Tetrahedron Lett. 31 (1990) 6269
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 6269
-
-
Graham, S.L.1
Scholz, T.H.2
-
17
-
-
0029862703
-
6- and 7-Substituted 2-[2′-(dimethylamino)ethyl]-1,2-dihydro-3H-dibenz[de,h]isoquinoline-1,3-diones: synthesis, nucleophilic displacements, antitumor activity, and quantitative structure-activity relationships
-
Sami S.M., Dorr R.T., Solyom A.M., Alberts D.S., Iyengar B.S., and Remers W.A. 6- and 7-Substituted 2-[2′-(dimethylamino)ethyl]-1,2-dihydro-3H-dibenz[de,h]isoquinoline-1,3-diones: synthesis, nucleophilic displacements, antitumor activity, and quantitative structure-activity relationships. J. Med. Chem. 39 (1996) 1609
-
(1996)
J. Med. Chem.
, vol.39
, pp. 1609
-
-
Sami, S.M.1
Dorr, R.T.2
Solyom, A.M.3
Alberts, D.S.4
Iyengar, B.S.5
Remers, W.A.6
-
18
-
-
0035018571
-
Synthesis of conjugated-bridged triphenylenes and applications in OLEDs
-
Freudenmann R., Behnisch B., and Hannack M. Synthesis of conjugated-bridged triphenylenes and applications in OLEDs. J. Mater. Chem. 11 (2001) 1618
-
(2001)
J. Mater. Chem.
, vol.11
, pp. 1618
-
-
Freudenmann, R.1
Behnisch, B.2
Hannack, M.3
-
19
-
-
0343920862
-
Synthesis of β-substituted naphth-1-ylethylamido derivatives as new melatoninergic agonists
-
Mathe-Allainmat M., Le Gall M., Jellimann C., Andrieux J., and Langlois M. Synthesis of β-substituted naphth-1-ylethylamido derivatives as new melatoninergic agonists. Bioorg. Med. Chem. 7 (1999) 2945
-
(1999)
Bioorg. Med. Chem.
, vol.7
, pp. 2945
-
-
Mathe-Allainmat, M.1
Le Gall, M.2
Jellimann, C.3
Andrieux, J.4
Langlois, M.5
-
20
-
-
0032542255
-
Repaglinide and related hypoglycemic benzoic acid derivatives
-
Grell W., Hurnaus R., Griss G., Sauter R., Rupprecht E., Mark M., Luger P., Nar H., Wittneben H., and Muller P. Repaglinide and related hypoglycemic benzoic acid derivatives. J. Med. Chem. 41 (1998) 5219
-
(1998)
J. Med. Chem.
, vol.41
, pp. 5219
-
-
Grell, W.1
Hurnaus, R.2
Griss, G.3
Sauter, R.4
Rupprecht, E.5
Mark, M.6
Luger, P.7
Nar, H.8
Wittneben, H.9
Muller, P.10
-
21
-
-
0034555493
-
Copper(I)-assisted mild and convenient synthesis of new Se-N heterocycles: access to a promising class of GPx mimics
-
Erdelmeier I., Tailhan-Lomont C., and Yadan J.C. Copper(I)-assisted mild and convenient synthesis of new Se-N heterocycles: access to a promising class of GPx mimics. J. Org. Chem. 65 (2000) 8152
-
(2000)
J. Org. Chem.
, vol.65
, pp. 8152
-
-
Erdelmeier, I.1
Tailhan-Lomont, C.2
Yadan, J.C.3
-
23
-
-
0017744326
-
Adrenergic agents. 6. Synthesis and potential β-adrenergic agonist activity of some meta-substituted p-hydroxyphenylethanolamines related to salbutamol
-
Jen T., Frazee J.S., Kaiser C., Colella D.F., and Wardell Jr. J.R. Adrenergic agents. 6. Synthesis and potential β-adrenergic agonist activity of some meta-substituted p-hydroxyphenylethanolamines related to salbutamol. J. Med. Chem. 20 (1977) 1029
-
(1977)
J. Med. Chem.
, vol.20
, pp. 1029
-
-
Jen, T.1
Frazee, J.S.2
Kaiser, C.3
Colella, D.F.4
Wardell Jr., J.R.5
-
24
-
-
18844460949
-
New reactions of nitriles. I. Amides from alkenes and mononitriles
-
Ritter J.J., and Minieri P.P. New reactions of nitriles. I. Amides from alkenes and mononitriles. J. Am. Chem. Soc. 70 (1948) 4045
-
(1948)
J. Am. Chem. Soc.
, vol.70
, pp. 4045
-
-
Ritter, J.J.1
Minieri, P.P.2
-
25
-
-
0002515902
-
Polyfluoroaralkylamines: an improved synthesis of 4,5,6,7-tetrafluoroindole
-
Filler R., Chen W., and Woods S.M. Polyfluoroaralkylamines: an improved synthesis of 4,5,6,7-tetrafluoroindole. J. Fluor. Chem. 73 (1995) 95
-
(1995)
J. Fluor. Chem.
, vol.73
, pp. 95
-
-
Filler, R.1
Chen, W.2
Woods, S.M.3
-
26
-
-
0000844829
-
Revised structure of bursatellin
-
Cimino G., Gavagnin M., Sodano G., Spinella A., and Strazzullo G. Revised structure of bursatellin. J. Org. Chem. 52 (1987) 2301
-
(1987)
J. Org. Chem.
, vol.52
, pp. 2301
-
-
Cimino, G.1
Gavagnin, M.2
Sodano, G.3
Spinella, A.4
Strazzullo, G.5
-
27
-
-
0034925279
-
A new and convenient synthesis of 1-aryl-2-dimethylaminoethanols
-
Nyerges M., Fejes I., Viranyi A., Groundwater P.W., and Toke L. A new and convenient synthesis of 1-aryl-2-dimethylaminoethanols. Synthesis (2001) 1479
-
(2001)
Synthesis
, pp. 1479
-
-
Nyerges, M.1
Fejes, I.2
Viranyi, A.3
Groundwater, P.W.4
Toke, L.5
-
28
-
-
33847800447
-
New fluorinating agents. Dialkylaminosulfur fluorides
-
Middleton W.J. New fluorinating agents. Dialkylaminosulfur fluorides. J. Org. Chem. 40 (1975) 574
-
(1975)
J. Org. Chem.
, vol.40
, pp. 574
-
-
Middleton, W.J.1
-
29
-
-
0029788578
-
Synthesis of imidazo[1,2-a]pyridines from pyridines and p-bromophenacyl bromide O-methyloxime
-
Artyomov V.A., Shestopalov A.M., and Litvinov V.P. Synthesis of imidazo[1,2-a]pyridines from pyridines and p-bromophenacyl bromide O-methyloxime. Synthesis (1996) 927
-
(1996)
Synthesis
, pp. 927
-
-
Artyomov, V.A.1
Shestopalov, A.M.2
Litvinov, V.P.3
-
30
-
-
0038601656
-
Synthesis of novel imidazo[1,2-a]pyridines with potent activity against herpesviruses
-
Gudmundsson K.S., and Johns B.A. Synthesis of novel imidazo[1,2-a]pyridines with potent activity against herpesviruses. Org. Lett. 5 (2003) 1369
-
(2003)
Org. Lett.
, vol.5
, pp. 1369
-
-
Gudmundsson, K.S.1
Johns, B.A.2
-
31
-
-
0032568905
-
One pot synthesis of 1-(2,2,6,6-tetramethyl-4-piperidinyl)-4-(4-fluorophenyl)-5-(2-amino-4-pyrimidinyl)-imidazole: a potent inhibitor of p38 MAP kinase
-
Sisko J.A. One pot synthesis of 1-(2,2,6,6-tetramethyl-4-piperidinyl)-4-(4-fluorophenyl)-5-(2-amino-4-pyrimidinyl)-imidazole: a potent inhibitor of p38 MAP kinase. J. Org. Chem. 63 (1998) 4529
-
(1998)
J. Org. Chem.
, vol.63
, pp. 4529
-
-
Sisko, J.A.1
-
33
-
-
0033549829
-
A highly active catalyst for the room-temperature amination and Suzuki coupling of aryl chlorides
-
Wolfe J.P., and Buchwald S.L. A highly active catalyst for the room-temperature amination and Suzuki coupling of aryl chlorides. Angew. Chem. Int. Ed. Engl. 38 (1999) 2413
-
(1999)
Angew. Chem. Int. Ed. Engl.
, vol.38
, pp. 2413
-
-
Wolfe, J.P.1
Buchwald, S.L.2
|