-
1
-
-
79952232216
-
Global Cancer Statistics
-
Jemal, A.; Bray, F.; Center, M. M.; Ferlay, J.; Ward, E.; Forman, D. Global Cancer Statistics CA Cancer J. Clin. 2011, 61, 69
-
(2011)
CA Cancer J. Clin.
, vol.61
, pp. 69
-
-
Jemal, A.1
Bray, F.2
Center, M.M.3
Ferlay, J.4
Ward, E.5
Forman, D.6
-
2
-
-
0036519363
-
DNA and its associated processes as targets for cancer therapy
-
Hurley, L. H. DNA and its associated processes as targets for cancer therapy Nat. Rev. Cancer 2002, 2, 188
-
(2002)
Nat. Rev. Cancer
, vol.2
, pp. 188
-
-
Hurley, L.H.1
-
3
-
-
0034707047
-
The DNA damage response: Putting checkpoints in perspective
-
Zhou, B.-B. S.; Elledge, S. J. The DNA damage response: Putting checkpoints in perspective Nature 2000, 408, 433
-
(2000)
Nature
, vol.408
, pp. 433
-
-
Zhou, B.-B.S.1
Elledge, S.J.2
-
4
-
-
4444344407
-
G2 checkpoint abrogators as anticancer drugs
-
Kawabe, T. G2 checkpoint abrogators as anticancer drugs Mol. Cancer Ther. 2004, 3, 513
-
(2004)
Mol. Cancer Ther.
, vol.3
, pp. 513
-
-
Kawabe, T.1
-
5
-
-
0037484271
-
Chk1 mediates S and G2 arrests through Cdc25A degradation in response to DNA-damaging agents
-
Xiao, Z.; Chen, Z.; Gunasekera, A. H.; Sowin, T. J.; Rosenberg, S. H.; Fesik, S.; Zhang, H. Chk1 mediates S and G2 arrests through Cdc25A degradation in response to DNA-damaging agents J. Biol. Chem. 2003, 278, 21767
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 21767
-
-
Xiao, Z.1
Chen, Z.2
Gunasekera, A.H.3
Sowin, T.J.4
Rosenberg, S.H.5
Fesik, S.6
Zhang, H.7
-
6
-
-
22844436238
-
Chk1 is essential for tumor cell viability following activation of the replication checkpoint
-
Cho, S. H.; Toouli, C. D.; Fujii, G. H.; Crain, C.; Parry, D. Chk1 is essential for tumor cell viability following activation of the replication checkpoint Cell Cycle 2005, 4, 131
-
(2005)
Cell Cycle
, vol.4
, pp. 131
-
-
Cho, S.H.1
Toouli, C.D.2
Fujii, G.H.3
Crain, C.4
Parry, D.5
-
7
-
-
47149114403
-
Novel inhibitors of checkpoint kinase 1
-
Arrington, K. L.; Dudkin, V. Y. Novel inhibitors of checkpoint kinase 1 ChemMedChem 2007, 2, 1571
-
(2007)
ChemMedChem
, vol.2
, pp. 1571
-
-
Arrington, K.L.1
Dudkin, V.Y.2
-
8
-
-
52949145309
-
Keeping checkpoint kinases in line: New selective inhibitors in clinical trials
-
Ashwell, S.; Janetka, J. W.; Zabludoff, S. Keeping checkpoint kinases in line: New selective inhibitors in clinical trials Expert Opin. Invest. Drugs 2008, 17, 1331
-
(2008)
Expert Opin. Invest. Drugs
, vol.17
, pp. 1331
-
-
Ashwell, S.1
Janetka, J.W.2
Zabludoff, S.3
-
9
-
-
53349156857
-
Breaching the DNA damage checkpoint via PF-00477736, a novel small-molecule inhibitor of checkpoint kinase 1
-
Blasina, A.; Hallin, J.; Chen, E.; Arango, M. E.; Kraynov, E.; Register, J.; Grant, S.; Ninkovic, S.; Chen, P.; Nichols, T.; O'Connor, P.; Anderes, K. Breaching the DNA damage checkpoint via PF-00477736, a novel small-molecule inhibitor of checkpoint kinase 1 Mol. Cancer Ther. 2008, 7, 2394
-
(2008)
Mol. Cancer Ther.
, vol.7
, pp. 2394
-
-
Blasina, A.1
Hallin, J.2
Chen, E.3
Arango, M.E.4
Kraynov, E.5
Register, J.6
Grant, S.7
Ninkovic, S.8
Chen, P.9
Nichols, T.10
O'Connor, P.11
Anderes, K.12
-
10
-
-
52949139387
-
AZD7762, a novel checkpoint kinase inhibitor, drives checkpoint abrogation and potentiates DNA-targeted therapies
-
Zabludoff, S. D.; Deng, C.; Grondine, M. R.; Sheehy, A. M.; Ashwell, S.; Caleb, B. L.; Green, S.; Haye, H. R.; Horn, C. L.; Janetka, J. W.; Liu, D.; Mouchet, E.; Ready, S.; Rosenthal, J. L.; Queva, C.; Schwartz, G. K.; Taylor, K. J.; Tse, A. N.; Walker, G. E.; White, A. M. AZD7762, a novel checkpoint kinase inhibitor, drives checkpoint abrogation and potentiates DNA-targeted therapies Mol. Cancer Ther. 2008, 7, 2955
-
(2008)
Mol. Cancer Ther.
, vol.7
, pp. 2955
-
-
Zabludoff, S.D.1
Deng, C.2
Grondine, M.R.3
Sheehy, A.M.4
Ashwell, S.5
Caleb, B.L.6
Green, S.7
Haye, H.R.8
Horn, C.L.9
Janetka, J.W.10
Liu, D.11
Mouchet, E.12
Ready, S.13
Rosenthal, J.L.14
Queva, C.15
Schwartz, G.K.16
Taylor, K.J.17
Tse, A.N.18
Walker, G.E.19
White, A.M.20
more..
-
11
-
-
79955735344
-
Targeting the replication checkpoint using SCH 900776, a potent and functionally selective CHK1 inhibitor identified via high content screening
-
Guzi, T. J.; Paruch, K.; Dwyer, M. P.; Labroli, M.; Shanahan, F.; Davis, N.; Taricani, L.; Wiswell, D.; Seghezzi, W.; Penaflor, E.; Bhagwat, B.; Wang, W.; Gu, D.; Hsieh, Y.; Lee, S.; Ming Liu, M.; Parry, D. Targeting the replication checkpoint using SCH 900776, a potent and functionally selective CHK1 inhibitor identified via high content screening Mol. Cancer Ther. 2011, 10, 591
-
(2011)
Mol. Cancer Ther.
, vol.10
, pp. 591
-
-
Guzi, T.J.1
Paruch, K.2
Dwyer, M.P.3
Labroli, M.4
Shanahan, F.5
Davis, N.6
Taricani, L.7
Wiswell, D.8
Seghezzi, W.9
Penaflor, E.10
Bhagwat, B.11
Wang, W.12
Gu, D.13
Hsieh, Y.14
Lee, S.15
Ming Liu, M.16
Parry, D.17
-
12
-
-
84884611511
-
ALIS: An Affinity Selection-Mass Spectrometry System for the Discovery and Characterization of Protein-Ligand Interactions
-
Wanner, K. Höfner, G. Mass Spectrometry in Medicinal Chemistry: Applications in Drug Discovery; Mannhold, R. Kubinyi, H. Folkers, G. Series; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Chapter 3
-
Annis, A.; Chuang, C.-C.; Nazef, N. ALIS: An Affinity Selection-Mass Spectrometry System for the Discovery and Characterization of Protein-Ligand Interactions. In Methods and Principles in Medicinal Chemistry; Wanner, K.; Höfner, G., Eds.; Mass Spectrometry in Medicinal Chemistry: Applications in Drug Discovery; Mannhold, R.; Kubinyi, H.; Folkers, G., Series Eds.; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, 2007; Vol. 36, Chapter 3.
-
(2007)
Methods and Principles in Medicinal Chemistry
, vol.36
-
-
Annis, A.1
Chuang, C.-C.2
Nazef, N.3
-
13
-
-
8444221197
-
An affinity selection-mass spectrometry method for the identification of small molecule ligands from self-encoded combinatorial libraries Discovery of a novel antagonist of E. coli dihydrofolate reductase
-
Annis, D. A.; Athanasopoulos, J.; Curran, P. J.; Felsch, J. S.; Kalghatgi, K.; Lee, W. H.; Nash, H. M.; Orminati, J.-P. A.; Rosner, K. E.; Shipps, G. W., Jr.; Thaddupathy, G. R. A.; Tylera, A. N.; Vilenchik, L.; Wagner, C. R.; Wintner, E. A. An affinity selection-mass spectrometry method for the identification of small molecule ligands from self-encoded combinatorial libraries Discovery of a novel antagonist of E. coli dihydrofolate reductase Int. J. Mass Spectrom. 2004, 238, 77
-
(2004)
Int. J. Mass Spectrom.
, vol.238
, pp. 77
-
-
Annis, D.A.1
Athanasopoulos, J.2
Curran, P.J.3
Felsch, J.S.4
Kalghatgi, K.5
Lee, W.H.6
Nash, H.M.7
Orminati, J.-P.A.8
Rosner, K.E.9
Shipps Jr., G.W.10
Thaddupathy, G.R.A.11
Tylera, A.N.12
Vilenchik, L.13
Wagner, C.R.14
Wintner, E.A.15
-
14
-
-
71749089252
-
Discovery and optimization of antibacterial AccC inhibitors
-
Cheng, C. C.; Shipps, G. W., Jr.; Yang, Z.; Sun, B.; Kawahata, N.; Soucy, K. A.; Soriano, A.; Orth, P.; Xiao, L.; Mann, P.; Black, T. Discovery and optimization of antibacterial AccC inhibitors Bioorg. Med. Chem. Lett. 2009, 19, 6507
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 6507
-
-
Cheng, C.C.1
Shipps Jr., G.W.2
Yang, Z.3
Sun, B.4
Kawahata, N.5
Soucy, K.A.6
Soriano, A.7
Orth, P.8
Xiao, L.9
Mann, P.10
Black, T.11
-
15
-
-
78650197292
-
Pyridine Carboxamides: Potent Palm Site Inhibitors of HCV NS5B Polymerase
-
Cheng, C. C.; Huang, X.; Shipps, G. W., Jr.; Wang, Y.-S.; Wyss, D. F.; Soucy, K. A.; Jiang, C.-k.; Agrawal, S.; Ferrari, E.; He, Z.; Huang, H.-C. Pyridine Carboxamides: Potent Palm Site Inhibitors of HCV NS5B Polymerase ACS Med. Chem. Lett. 2010, 1, 466
-
(2010)
ACS Med. Chem. Lett.
, vol.1
, pp. 466
-
-
Cheng, C.C.1
Huang, X.2
Shipps Jr., G.W.3
Wang, Y.-S.4
Wyss, D.F.5
Soucy, K.A.6
Jiang, C.-K.7
Agrawal, S.8
Ferrari, E.9
He, Z.10
Huang, H.-C.11
-
16
-
-
77949487755
-
Inhibitors of hepatitis C virus polymerase: Synthesis and characterization of novel 2-oxy-6-fluoro-N-((S)-1-hydroxy-3-phenylpropan-2-yl)- benzamides
-
Cheng, C. C.; Shipps, G. W., Jr.; Yang, Z.; Kawahata, N.; Lesburg, C. A.; Duca, J. S.; Bandouveres, J.; Bracken, J. D.; Jiang, C.-k.; Agrawal, S.; Ferrari, E.; Huang, H.-C. Inhibitors of hepatitis C virus polymerase: Synthesis and characterization of novel 2-oxy-6-fluoro-N-((S)-1-hydroxy-3-phenylpropan-2- yl)-benzamides Bioorg. Med. Chem. Lett. 2010, 20, 2119
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 2119
-
-
Cheng, C.C.1
Shipps Jr., G.W.2
Yang, Z.3
Kawahata, N.4
Lesburg, C.A.5
Duca, J.S.6
Bandouveres, J.7
Bracken, J.D.8
Agrawal, S.9
Ferrari, E.10
Huang, H.-C.11
-
17
-
-
9644265255
-
Aminothiazole inhibitors of HCV RNA polymerase
-
Shipps, G. W., Jr.; Deng, Y.; Wang, T.; Popovici-Muller, J.; Curran, P. J.; Rosner, K. E.; Cooper, A. B.; Girijavallabhan, V.; Butkiewicz, N.; Cable, M. Aminothiazole inhibitors of HCV RNA polymerase Bioorg. Med. Chem. Lett. 2005, 15, 115
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 115
-
-
Shipps Jr., G.W.1
Deng, Y.2
Wang, T.3
Popovici-Muller, J.4
Curran, P.J.5
Rosner, K.E.6
Cooper, A.B.7
Girijavallabhan, V.8
Butkiewicz, N.9
Cable, M.10
-
18
-
-
34347224752
-
Method for quantitative protein-ligand affinity measurements in compound mixtures
-
Annis, D. A.; Shipps, G. W., Jr.; Deng, Y.; Popovici-Müller, J.; Siddiqui, M. A.; Curran, P. J.; Gowen, M.; Windsor, W. T. Method for quantitative protein-ligand affinity measurements in compound mixtures Anal. Chem. 2007, 79, 4538
-
(2007)
Anal. Chem.
, vol.79
, pp. 4538
-
-
Annis, D.A.1
Shipps Jr., G.W.2
Deng, Y.3
Popovici-Müller, J.4
Siddiqui, M.A.5
Curran, P.J.6
Gowen, M.7
Windsor, W.T.8
-
19
-
-
66349112547
-
Substituted benzimidazoles: A novel chemotype for small molecule h ksp inhibitors
-
Lahue, B. R.; Ma, Y.; Shipps, G. W., Jr.; Seghezzi, W.; Herbst, R. Substituted benzimidazoles: a novel chemotype for small molecule h ksp inhibitors Bioorg. Med. Chem. Lett. 2009, 19, 3405
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 3405
-
-
Lahue, B.R.1
Ma, Y.2
Shipps Jr., G.W.3
Seghezzi, W.4
Herbst, R.5
-
20
-
-
79953315358
-
Small-molecule inhibitors of FABP4/5 ameliorate dyslipidemia but not insulin resistance in mice with diet-induced obesity
-
Lan, H.; Cheng, C. C.; Kowalski, T. J.; Pang, L.; Shan, L.; Chuang, C.-C.; Jackson, J.; Rojas-Triana, A.; Bober, L.; Liu, L.; Voigt, J.; Orth, P.; Yang, X.; Shipps, G. W., Jr.; Hedrick, J. A. Small-molecule inhibitors of FABP4/5 ameliorate dyslipidemia but not insulin resistance in mice with diet-induced obesity J. Lipid Res. 2011, 52, 646
-
(2011)
J. Lipid Res.
, vol.52
, pp. 646
-
-
Lan, H.1
Cheng, C.C.2
Kowalski, T.J.3
Pang, L.4
Shan, L.5
Chuang, C.-C.6
Jackson, J.7
Rojas-Triana, A.8
Bober, L.9
Liu, L.10
Voigt, J.11
Orth, P.12
Yang, X.13
Shipps Jr., G.W.14
Hedrick, J.A.15
-
21
-
-
69749122834
-
Inhibitors of the lipid phosphatase SHIP2 discovered by high throughput affinity selection-mass spectrometry screening of combinatorial libraries
-
Annis, D. A.; Cheng, C. C.; Chuang, C.-C.; McCarter, J. D.; Nash, H. M.; Nazef, N.; Rowe, T.; Kurzeja, R. J. M.; Shipps, G. W., Jr. Inhibitors of the lipid phosphatase SHIP2 discovered by high throughput affinity selection-mass spectrometry screening of combinatorial libraries Comb. Chem. High Throughput Screen. 2009, 12, 760
-
(2009)
Comb. Chem. High Throughput Screen.
, vol.12
, pp. 760
-
-
Annis, D.A.1
Cheng, C.C.2
Chuang, C.-C.3
McCarter, J.D.4
Nash, H.M.5
Nazef, N.6
Rowe, T.7
Kurzeja, R.J.M.8
Shipps Jr., G.W.9
-
22
-
-
80051744356
-
Discovery and hit-to-lead optimization of non-ATP competitive MK2 (MAPKAPK2) inhibitors
-
Huang, X.; Shipps, G. W., Jr.; Cheng, C. C.; Spacciapoli, P.; Zhang, X.; McCoy, M. A.; Wyss, D. F.; Yang, X.; Achab, A.; Soucy, K.; Montavon, D. K.; Murphy, D. M.; Whitehurst, C. E. Discovery and hit-to-lead optimization of non-ATP competitive MK2 (MAPKAPK2) inhibitors ACS Med. Chem. Lett. 2011, 2, 632
-
(2011)
ACS Med. Chem. Lett.
, vol.2
, pp. 632
-
-
Huang, X.1
Shipps Jr., G.W.2
Cheng, C.C.3
Spacciapoli, P.4
Zhang, X.5
McCoy, M.A.6
Wyss, D.F.7
Yang, X.8
Achab, A.9
Soucy, K.10
Montavon, D.K.11
Murphy, D.M.12
Whitehurst, C.E.13
-
23
-
-
74049143519
-
The discovery of novel tartrate-based TNF-α converting enzyme (TACE) inhibitors
-
Rosner, K. E.; Guo, Z.; Orth, P.; Shipps, G. W., Jr.; Belanger, D. B.; Chan, T. Y.; Curran, P. J.; Dai, C.; Deng, Y.; Girijavallabhan, V. M.; Hong, L.; Lavey, B. J.; Lee, J. F.; Li, D.; Liu, Z.; Popovici-Muller, J.; Ting, P. C.; Vaccaro, H.; Wang, L.; Wang, T.; Yu, W.; Zhou, G.; Niu, X.; Sun, J.; Kozlowski, J. A.; Lundell, D. J.; Madison, V.; McKittrick, B.; Piwinski, J. J.; Shih, N.-Y.; Siddiqui, M. A.; Strickland, C. O. The discovery of novel tartrate-based TNF-α converting enzyme (TACE) inhibitors Bioorg. Med. Chem. Lett. 2009, 20, 1189
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 1189
-
-
Rosner, K.E.1
Guo, Z.2
Orth, P.3
Shipps Jr., G.W.4
Belanger, D.B.5
Chan, T.Y.6
Curran, P.J.7
Dai, C.8
Deng, Y.9
Girijavallabhan, V.M.10
Hong, L.11
Lavey, B.J.12
Lee, J.F.13
Li, D.14
Liu, Z.15
Popovici-Muller, J.16
Ting, P.C.17
Vaccaro, H.18
Wang, L.19
Wang, T.20
Yu, W.21
Zhou, G.22
Niu, X.23
Sun, J.24
Kozlowski, J.A.25
Lundell, D.J.26
Madison, V.27
McKittrick, B.28
Piwinski, J.J.29
Shih, N.-Y.30
Siddiqui, M.A.31
Strickland, C.O.32
more..
-
24
-
-
33644934750
-
2 acetylcholine receptor ligands by affinity selection-mass spectrometry
-
2 acetylcholine receptor ligands by affinity selection-mass spectrometry J. Biomol. Screen. 2006, 11, 194
-
(2006)
J. Biomol. Screen.
, vol.11
, pp. 194
-
-
Whitehurst, C.E.1
Nazef, N.2
Annis, D.A.3
Hou, Y.4
Murphy, D.M.5
Spacciapoli, P.6
Yao, Z.7
Ziebell, M.R.8
Cheng, C.C.9
Shipps Jr., G.W.10
Felsch, J.S.11
Lau, D.12
Nash, H.M.13
-
25
-
-
0029880622
-
Suppression of apoptosis by dominant negative mutants of cyclin-dependent protein kinases
-
Meikrantz, W.; Schlegel, R. Suppression of apoptosis by dominant negative mutants of cyclin-dependent protein kinases J. Biol. Chem. 1996, 271, 10205
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 10205
-
-
Meikrantz, W.1
Schlegel, R.2
-
26
-
-
0036765313
-
Inhibition of cyclin-dependent kinase 2 by the Chk1-Cdc25A pathway during the S-phase checkpoint activated by fludarabine: Dysregulation by 7-hydroxystaurosporine
-
Sampath, D.; Shi, Z.; Plunkett, W. Inhibition of cyclin-dependent kinase 2 by the Chk1-Cdc25A pathway during the S-phase checkpoint activated by fludarabine: dysregulation by 7-hydroxystaurosporine Mol. Pharmacol. 2002, 62, 680
-
(2002)
Mol. Pharmacol.
, vol.62
, pp. 680
-
-
Sampath, D.1
Shi, Z.2
Plunkett, W.3
-
27
-
-
9644302954
-
A general technique to rank protein-ligand binding affinities and determine allosteric versus direct binding site competition in compound mixtures
-
Annis, D. A.; Nazef, N.; Chuang, C.-C.; Scott, M. P.; Nash, H. M. A general technique to rank protein-ligand binding affinities and determine allosteric versus direct binding site competition in compound mixtures J. Am. Chem. Soc. 2004, 126, 15495
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 15495
-
-
Annis, D.A.1
Nazef, N.2
Chuang, C.-C.3
Scott, M.P.4
Nash, H.M.5
-
28
-
-
85171909122
-
-
WO 2007/058942 A2
-
Zhao, L.; Curran, P. J.; Belanger, D. B.; Hamann, B.; Reddy, P. A.; Paruch, K.; Guzi, T. J.; Dwyer, M. P.; Siddiqui, M. A.; Tadikonda, P. K. Imidazopyrazines as protein kinase inhibitors. WO 2007/058942 A2.
-
Imidazopyrazines As Protein Kinase Inhibitors
-
-
Zhao, L.1
Curran, P.J.2
Belanger, D.B.3
Hamann, B.4
Reddy, P.A.5
Paruch, K.6
Guzi, T.J.7
Dwyer, M.P.8
Siddiqui, M.A.9
Tadikonda, P.K.10
-
29
-
-
0036893503
-
Kinase inhibitors and the case for CH⋯O hydrogen bonds in protein-ligand binding
-
Pierce, A. C.; Sandretto, K. L.; Bemis, G. W. Kinase inhibitors and the case for CH⋯O hydrogen bonds in protein-ligand binding Proteins: Struct. Funct. Genet 2002, 49, 567
-
(2002)
Proteins: Struct. Funct. Genet
, vol.49
, pp. 567
-
-
Pierce, A.C.1
Sandretto, K.L.2
Bemis, G.W.3
-
30
-
-
77949799227
-
Intramolecular hydrogen bonding in medicinal chemistry
-
Kuhn, B.; Mohr, P.; Stahl, M. Intramolecular hydrogen bonding in medicinal chemistry J. Med. Chem. 2010, 53, 2601
-
(2010)
J. Med. Chem.
, vol.53
, pp. 2601
-
-
Kuhn, B.1
Mohr, P.2
Stahl, M.3
-
31
-
-
33847655150
-
Classification of water molecules in protein binding sites
-
Barillari, C.; Taylor, J.; Viner, R.; Essex, J. W. Classification of water molecules in protein binding sites J. Am. Chem. Soc. 2007, 129, 2577
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 2577
-
-
Barillari, C.1
Taylor, J.2
Viner, R.3
Essex, J.W.4
-
32
-
-
78650514817
-
Discovery of pyrazolo[1,5 - A ]pyrimidine-based CHK1 inhibitors: A template-based approach-Part 1
-
Dwyer, M. P.; Paruch, K.; Labroli, M.; Alvarez, C.; Keertikar, K. M.; Poker, C.; Rossman, R.; Fischmann, T. O.; Duca, J. S.; Madison, V.; Parry, D.; Davis, N.; Seghezzi, W.; Wiswell, D.; Guzi, T. J. Discovery of pyrazolo[1,5- a ]pyrimidine-based CHK1 inhibitors: A template-based approach-Part 1 Bioorg. Med. Chem. Lett. 2011, 21, 467
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 467
-
-
Dwyer, M.P.1
Paruch, K.2
Labroli, M.3
Alvarez, C.4
Keertikar, K.M.5
Poker, C.6
Rossman, R.7
Fischmann, T.O.8
Duca, J.S.9
Madison, V.10
Parry, D.11
Davis, N.12
Seghezzi, W.13
Wiswell, D.14
Guzi, T.J.15
-
33
-
-
33746256441
-
A highly active catalyst for Suzuki-Miyaura cross-coupling reactions of heteroaryl compounds
-
Billingsley, K. L.; Anderson, K. W.; Buchwald, S. L. A highly active catalyst for Suzuki-Miyaura cross-coupling reactions of heteroaryl compounds Angew. Chem., Int. Ed. 2006, 45, 3484
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 3484
-
-
Billingsley, K.L.1
Anderson, K.W.2
Buchwald, S.L.3
-
34
-
-
0347985383
-
Efficient palladium-catalyzed coupling of aryl chlorides and tosylates with terminal alkynes: Use of a copper cocatalyst inhibits the reaction
-
Gelman, D.; Buchwald, S. L. Efficient palladium-catalyzed coupling of aryl chlorides and tosylates with terminal alkynes: Use of a copper cocatalyst inhibits the reaction Angew. Chem., Int. Ed. 2003, 42, 5993
-
(2003)
Angew. Chem., Int. Ed.
, vol.42
, pp. 5993
-
-
Gelman, D.1
Buchwald, S.L.2
|