-
1
-
-
0037486826
-
Carbon-Carbon Bond Formations Involving Organochromium(III) Reagents
-
Fürstner, A. Carbon-carbon bond formations involving organochromium(III) reagents. Chem. Rev. 1999, 99, 991-1045. (Pubitemid 129589772)
-
(1999)
Chemical Reviews
, vol.99
, Issue.4
, pp. 991-1045
-
-
Furstner, A.1
-
2
-
-
13644268558
-
Regioselective cross-coupling reactions of multiple halogenated nitrogen-, oxygen-, and sulfur-containing heterocycles
-
DOI 10.1016/j.tet.2004.11.074
-
Schröter, S.; Stock, C.; Bach, T. Regioselective cross-coupling reactions of multiple halogenated nitrogen-, oxygen-, and sulfur-containing heterocycles. Tetrahedron 2005, 61, 2245-2267. (Pubitemid 40228786)
-
(2005)
Tetrahedron
, vol.61
, Issue.9
, pp. 2245-2267
-
-
Schroter, S.1
Stock, C.2
Bach, T.3
-
3
-
-
33846918696
-
Aryl-aryl bond formation by transition-metal-catalyzed direct arylation
-
DOI 10.1021/cr0509760
-
Alberico, D.; Scott, M.E.; Lautens, M. Aryl-aryl bond formation by transition-metal-catalyzed direct arylation. Chem. Rev. 2007, 107, 174-238. (Pubitemid 46237369)
-
(2007)
Chemical Reviews
, vol.107
, Issue.1
, pp. 174-238
-
-
Alberico, D.1
Scott, M.E.2
Lautens, M.3
-
4
-
-
77949587544
-
Cobalt-catalyzed cross-coupling reactions
-
Cahiez, G.; Moyeux, A. Cobalt-catalyzed cross-coupling reactions. Chem. Rev. 2010, 110, 1435-1462.
-
(2010)
Chem. Rev
, vol.110
, pp. 1435-1462
-
-
Cahiez, G.1
Moyeux, A.2
-
5
-
-
79952656192
-
Advances in transition metal (Pd,Ni,Fe)-catalyzed crosscoupling reactions using alkyl-organometallics as reaction partners
-
Jana, R.; Pathak, T.P.; Sigman, M.S. Advances in transition metal (Pd,Ni,Fe)-catalyzed crosscoupling reactions using alkyl-organometallics as reaction partners. Chem. Rev. 2011, 111, 1417-1492.
-
(2011)
Chem. Rev
, vol.111
, pp. 1417-1492
-
-
Jana, R.1
Pathak, T.P.2
Sigman, M.S.3
-
7
-
-
77956908369
-
Exploration of piperidine-4-yl-aminopyrimidines as HIV-1 reverse transcriptase inhibitors. N-Phenyl derivatives with broad potency against resistant mutant viruses
-
Tang, G.; Kertesz, D.J.; Yang, M.; Lin, X.; Wang, Z.; Li, W.; Qiu, Z.; Chen, J.; Mei, J.; Chen, L.; et al. Exploration of piperidine-4-yl- aminopyrimidines as HIV-1 reverse transcriptase inhibitors. N-Phenyl derivatives with broad potency against resistant mutant viruses. Bioorg. Med. Chem. Lett. 2010, 20, 6020-6023.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, pp. 6020-6023
-
-
Tang, G.1
Kertesz, D.J.2
Yang, M.3
Lin, X.4
Wang, Z.5
Li, W.6
Qiu, Z.7
Chen, J.8
Mei, J.9
Chen, L.10
-
8
-
-
34250159423
-
2B adenosine receptor antagonist
-
DOI 10.1021/jm061333v
-
Vidal, B.; Nueda, A.; Esteve, C.; Domenech, T.; Benito, S.; Reinoso, R.F.; Pont, M.; Calbet, M.; Lopez, R.; Cadavid, M.I.; et al. Discovery and characterization of 4'-(2-furyl)-N-pyridin-3-yl-4,5' bipyrimidin-2'-amine (LAS38096), a potent, selective, and efficacious A2B adenosine receptor antagonist. J. Med. Chem. 2007, 50, 2732-2736. (Pubitemid 46896081)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.11
, pp. 2732-2736
-
-
Vidal, B.1
Nueda, A.2
Esteve, C.3
Domenech, T.4
Benito, S.5
Reinoso, R.F.6
Pont, M.7
Calbet, M.8
Lopez, R.9
Cadavid, M.I.10
Loza, M.I.11
Cardenas, A.12
Godessart, N.13
Beleta, J.14
Warrellow, G.15
Ryder, H.16
-
9
-
-
52449106253
-
The identification of 2-(1H-indazol-4-yl)-6-(4- methanesulfonyl- piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class i PI3 kinase for the treatment of cancer
-
Folkes, A.J.; Ahmadi, K.; Alderton, W.K.; Alix, S.; Baker, S.J.; Box, G.; Chuckowree, I.S.; Clarke, P.A.; Depledge, P.; Eccles, S.A.; et al. The identification of 2-(1H-indazol-4-yl)-6-(4- methanesulfonyl-piperazin-1- ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class I PI3 kinase for the treatment of cancer. J. Med. Chem. 2008, 51, 5522-5532.
-
(2008)
J. Med. Chem
, vol.51
, pp. 5522-5532
-
-
Folkes, A.J.1
Ahmadi, K.2
Alderton, W.K.3
Alix, S.4
Baker, S.J.5
Box, G.6
Chuckowree, I.S.7
Clarke, P.A.8
Depledge, P.9
Eccles, S.A.10
-
10
-
-
73249124369
-
Discovery of 4-morpholino-6-aryl-1Hpyrazolo[ 3,4-d]pyrimidines as highly potent and selective ATP-competitive inhibitors of the mammalian target of rapamycin (mTOR): Optimization of the 6-aryl substituent
-
Verheijen, J.C.; Richard, D.J.; Curran, K.; Kaplan, J.; Lefever, M.; Nowak, P.; Malwitz, D.J.; Brooijmans, N.; Toral-Barza, L.; Zhang, W.-G.; et al. Discovery of 4-morpholino-6-aryl-1Hpyrazolo[ 3,4-d]pyrimidines as highly potent and selective ATP-competitive inhibitors of the mammalian target of rapamycin (mTOR): optimization of the 6-aryl substituent. J. Med. Chem. 2009, 52, 8010-8024.
-
(2009)
J. Med. Chem
, vol.52
, pp. 8010-8024
-
-
Verheijen, J.C.1
Richard, D.J.2
Curran, K.3
Kaplan, J.4
Lefever, M.5
Nowak, P.6
Malwitz, D.J.7
Brooijmans, N.8
Toral-Barza, L.9
Zhang, W.-G.10
-
11
-
-
77249137785
-
Discovery of (thienopyrimidin-2- yl)aminopyrimidines as potent, selective, and orally available pan-PI3-kinase and dual pan-PI3- kinase/mTOR inhibitors for the treatment of cancer
-
Sutherlin, D.P.; Sampath, D.; Berry, M.; Castanedo, G.; Chang, Z.; Chuckowree, I.; Dotson, J.; Folkes, A.; Friedman, L.; Goldsmith, R.; et al. Discovery of (thienopyrimidin-2- yl)aminopyrimidines as potent, selective, and orally available pan-PI3-kinase and dual pan-PI3- kinase/mTOR inhibitors for the treatment of cancer. J. Med. Chem. 2010, 53, 1086-1097.
-
(2010)
J. Med. Chem
, vol.53
, pp. 1086-1097
-
-
Sutherlin, D.P.1
Sampath, D.2
Berry, M.3
Castanedo, G.4
Chang, Z.5
Chuckowree, I.6
Dotson, J.7
Folkes, A.8
Friedman, L.9
Goldsmith, R.10
-
12
-
-
20844448572
-
Novel and efficient access to phenylamino-pyrimidine type protein kinase C inhibitors utilizing a Negishi cross-coupling strategy
-
DOI 10.1021/jo0505223
-
Stanetty, P.; Hattinger, G.; Schnürch, M.; Mihovilovic, M.D. Novel and efficient access to phenylamino-pyrimidine type protein kinase C inhibitors utilizing a Negishi cross-coupling strategy. J. Org. Chem. 2005, 70, 5215-5220. (Pubitemid 40863927)
-
(2005)
Journal of Organic Chemistry
, vol.70
, Issue.13
, pp. 5215-5220
-
-
Stanetty, P.1
Hattinger, G.2
Schnurch, M.3
Mihovilovic, M.D.4
-
13
-
-
78651479722
-
Synthesis and in vitro and in vivo evaluation of phosphoinositide-3- kinase inhibitors
-
Burger, M.T.; Knapp, M.; Wagman, A.; Ni, Z.-J.; Hendrickson, T.; Atallah, G.; Zhang, Y.; Frazier, K.; Verhagen, J.; Pfister, K.; et al. Synthesis and in vitro and in vivo evaluation of phosphoinositide-3-kinase inhibitors. ACS Med. Chem. Lett. 2011, 2, 34-38.
-
(2011)
ACS Med. Chem. Lett
, vol.2
, pp. 34-38
-
-
Burger, M.T.1
Knapp, M.2
Wagman, A.3
Ni, Z.-J.4
Hendrickson, T.5
Atallah, G.6
Zhang, Y.7
Frazier, K.8
Verhagen, J.9
Pfister, K.10
-
14
-
-
74849136062
-
Synthesis, biological evaluation, x-ray structure, and pharmacokinetics of aminopyrimidine c-jun-N-terminal kinase (JNK) inhibitors
-
Kamenecka, T.; Jiang, R.; Song, X.; Duckett, D.; Chen, W.; Ling, Y.Y.; Habel, J.; Laughlin, J.D.; Chambers, J.; Figuera-Losada, M.; et al. Synthesis, biological evaluation, x-ray structure, and pharmacokinetics of aminopyrimidine c-jun-N-terminal kinase (JNK) inhibitors. J. Med. Chem. 2010, 53, 419-431.
-
(2010)
J. Med. Chem
, vol.53
, pp. 419-431
-
-
Kamenecka, T.1
Jiang, R.2
Song, X.3
Duckett, D.4
Chen, W.5
Ling, Y.Y.6
Habel, J.7
Laughlin, J.D.8
Chambers, J.9
Figuera-Losada, M.10
-
15
-
-
56749178895
-
Cis-4-(Piperazin-1-yl)-5,6,7a,8,9,10,11,11aoctahydrobenzofuro[ 2,3-h]quinazolin-2-amine (A-987306), a new histamine H4R antagonist that blocks pain responses against carrageenan-induced hyperalgesia
-
Liu, H.; Altenbach, R.J.; Carr, T.L.; Chandran, P.; Hsieh, G.C.; Lewis, L.G.R.; Manelli, A.M.; Milicic, I.; Marsh, K.C.; Miller, T.R.; et al. cis-4-(Piperazin-1-yl)-5,6,7a,8,9,10,11,11aoctahydrobenzofuro[ 2,3-h]quinazolin-2-amine (A-987306), a new histamine H4R antagonist that blocks pain responses against carrageenan-induced hyperalgesia. J. Med Chem. 2008, 51, 7094-7098.
-
(2008)
J. Med Chem
, vol.51
, pp. 7094-7098
-
-
Liu, H.1
Altenbach, R.J.2
Carr, T.L.3
Chandran, P.4
Hsieh, G.C.5
Lewis, L.G.R.6
Manelli, A.M.7
Milicic, I.8
Marsh, K.C.9
Miller, T.R.10
-
16
-
-
34547556499
-
Novel vanilloid receptor-1 antagonists: 3. The identification of a second-generation clinical candidate with improved physicochemical and pharmacokinetic properties
-
DOI 10.1021/jm070191h
-
Wang, H.-L.; Katon, J.; Balan, C.; Bannon, A.W.; Bernard, C.; Doherty, E.M.; Dominguez, C.; Gavva, N.R.; Gore, V.; Ma, V.; et al. Novel vanilloid receptor-1 antagonists: 3. The identification of a second-generation clinical candidate with improved physicochemical and pharmacokinetic properties. J. Med. Chem. 2007, 50, 3528-3539. (Pubitemid 47195461)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.15
, pp. 3528-3539
-
-
Wang, H.-L.1
Katon, J.2
Balan, C.3
Bannon, A.W.4
Bernard, C.5
Doherty, E.M.6
Dominguez, C.7
Gavva, N.R.8
Gore, V.9
Ma, V.10
Nishimura, N.11
Surapaneni, S.12
Tang, P.13
Tamir, R.14
Thiel, O.15
Treanor, J.J.S.16
Norman, M.H.17
-
17
-
-
42949108141
-
Design and synthesis of peripherally restricted transient receptor potential vanilloid 1 (TRPV1) antagonists
-
DOI 10.1021/jm7014638
-
Tamayo, N.; Liao, H.; Stec, M.M.; Wang, X.; Chakrabarti, P.; Retz, D.; Doherty, E.M.; Surapaneni, S.; Tamir, R.; Bannon, A.W.; et al. Design and synthesis of peripherally restricted transient receptor potential vanilloid 1 (TRPV1) antagonists. J. Med. Chem. 2008, 51, 2744-2757. (Pubitemid 351620796)
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, Issue.9
, pp. 2744-2757
-
-
Tamayo, N.1
Liao, H.2
Stec, M.M.3
Wang, X.4
Chakrabarti, P.5
Retz, D.6
Doherty, E.M.7
Surapaneni, S.8
Tamir, R.9
Bannon, A.W.10
Gavva, N.R.11
Norman, M.H.12
-
18
-
-
0035914021
-
Arylation of halogenated pyrimidines via a suzuki coupling reaction
-
DOI 10.1021/jo010573+
-
Schomaker, J.M.; Delia, T.J. Arylation of halogenated pyrimidines via Suzuki coupling. J. Org. Chem. 2001, 66, 7125-7128. (Pubitemid 32983102)
-
(2001)
Journal of Organic Chemistry
, vol.66
, Issue.21
, pp. 7125-7128
-
-
Schomaker, J.M.1
Delia, T.J.2
-
19
-
-
0037112673
-
Palladium-catalyzed coupling reactions of aryl chlorides
-
Littke, A.F.; Fu, G.C. Palladium-catalyzed coupling reactions of aryl chlorides. Angew. Chem. Int. Ed. 2002, 41, 4179-4211.
-
(2002)
Angew. Chem. Int. Ed
, vol.41
, pp. 4179-4211
-
-
Littke, A.F.1
Fu, G.C.2
-
20
-
-
13444263825
-
Catalysts for cross-coupling reactions with non-activated alkyl halides
-
DOI 10.1002/anie.200461432
-
Frisch, A.C.; Beller, M. Catalysts for cross-coupling reactions with non-activated alkyl halides. Angew. Chem. Int. Ed. 2005, 44, 674-688. (Pubitemid 40203976)
-
(2005)
Angewandte Chemie - International Edition
, vol.44
, Issue.5
, pp. 674-688
-
-
Frisch, A.C.1
Beller, M.2
-
21
-
-
33846893890
-
Carbon-carbon coupling reactions catalyzed by heterogeneous palladium catalysts
-
DOI 10.1021/cr0505674
-
Yin, L.; Liebscher, J. Carbon-carbon coupling reactions catalyzed by heterogeneous palladium catalysts. Chem. Rev. 2007, 107, 133-173. (Pubitemid 46223705)
-
(2007)
Chemical Reviews
, vol.107
, Issue.1
, pp. 133-173
-
-
Yin, L.1
Liebscher, J.2
-
22
-
-
84989481284
-
Use of sacrificial anodes in electrochemical functionalization of organic halides
-
Chaussard, J.; Folest, J.-C.; Nédélec, J.-Y.; Périchon, J.; Sibille, S.; Troupel, M. Use of sacrificial anodes in electrochemical functionalization of organic halides. Synthesis 1990, 5, 369-381.
-
(1990)
Synthesis
, vol.5
, pp. 369-381
-
-
Chaussard, J.1
Folest, J.-C.2
Nédélec, J.-Y.3
Périchon, J.4
Sibille, S.5
Troupel, M.6
-
23
-
-
34547122209
-
Preparation of functionalized aryl- and heteroarylpyridazines by nickel-catalyzed electrochemical cross-coupling reactions
-
DOI 10.1021/jo070429+
-
Sengmany, S.; Léonel, E.; Polissaint, F.; Nédélec, J.-Y.; Pipelier, M.; Thobie-Gautier, C.; Dubreuil, D. Preparation of functionalized aryl- and heteroarylpyridazines by nickel-catalyzed electrochemical cross-coupling reactions. J. Org. Chem. 2007, 72, 5631-5636. (Pubitemid 47104665)
-
(2007)
Journal of Organic Chemistry
, vol.72
, Issue.15
, pp. 5631-5636
-
-
Sengmany, S.1
Leonel, E.2
Polissaint, F.3
Nedelec, J.-Y.4
Pipelier, M.5
Thobie-Gautier, C.6
Dubreuil, D.7
-
24
-
-
77950930483
-
Some mechanistic aspects of a nickel-catalyzed electrochemical cross-coupling between aryl halides and substituted chloropyridazines
-
Urgin, K.; Barhdadi, R.; Condon, S.; Léonel, E.; Pipelier, M.; Blot, V.; Thobie-Gautier, C.; Dubreuil, D. Some mechanistic aspects of a nickel-catalyzed electrochemical cross-coupling between aryl halides and substituted chloropyridazines. Electrochimica Acta 2010, 55, 4495-4500.
-
(2010)
Electrochimica Acta
, vol.55
, pp. 4495-4500
-
-
Urgin, K.1
Barhdadi, R.2
Condon, S.3
Léonel, E.4
Pipelier, M.5
Blot, V.6
Thobie-Gautier, C.7
Dubreuil, D.8
-
25
-
-
0343851067
-
Electrochemical cross-coupling between functionalized aryl halides and 2-chloropyrimidine or 2-chloropyrazine catalyzed by nickel 2,2'-bipyridine complex
-
PII S0040403999020377
-
Gosmini, C.; Nédélec, J.-Y.; Périchon, J. Electrochemical cross-coupling between functionalized aryl halides and 2-chloropyrimidine or 2-chloropyrazine catalyzed by nickel 2,2'-bipyridine complex. Tetrahedron Lett. 2000, 41, 201-203. (Pubitemid 30014601)
-
(2000)
Tetrahedron Letters
, vol.41
, Issue.2
, pp. 201-203
-
-
Gosmini, C.1
Nedelec, J.Y.2
Perichon, J.3
-
26
-
-
0035825062
-
Cobalt-catalyzed electrochemical cross-coupling of functionalized phenyl halides with 4-chloroquinoline derivatives
-
DOI 10.1016/S0040-4039(00)01936-5, PII S0040403900019365
-
Le Gall, E.; Gosmini, C.; Nédélec, J.-Y.; Périchon, J. Cobalt-catalyzed electrochemical crosscoupling of functionalized phenyl halides with 4-chloroquinoline derivatives. Tetrahedron Lett. 2001, 42, 267-269. (Pubitemid 32332679)
-
(2001)
Tetrahedron Letters
, vol.42
, Issue.2
, pp. 267-269
-
-
Le Gall, E.1
Gosmini, C.2
Nedelec, J.-Y.3
Perichon, J.4
-
27
-
-
72049089060
-
2,4-Diaminopyrimidines as histamine H4 receptor ligands-Scaffold optimization and pharmacological characterization
-
Sander, K.; Kottke, T.; Tanrikulu, Y.; Proschak, E.; Weizel, L.; Schneider, E.H.; Seifert, R.; Schneider, G.; Stark, H. 2,4-Diaminopyrimidines as histamine H4 receptor ligands-Scaffold optimization and pharmacological characterization. Bioorg. Med. Chem. 2009, 17, 7186-7196.
-
(2009)
Bioorg. Med. Chem
, vol.17
, pp. 7186-7196
-
-
Sander, K.1
Kottke, T.2
Tanrikulu, Y.3
Proschak, E.4
Weizel, L.5
Schneider, E.H.6
Seifert, R.7
Schneider, G.8
Stark, H.9
-
28
-
-
0001419923
-
Organic electroreductive coupling reactions using transition metal complexes as catalysts
-
Nédélec, J.-Y.; Périchon, J.; Troupel, M. Organic electroreductive coupling reactions using transition metal complexes as catalysts. Top. Curr. Chem. 1997, 185, 141-173.
-
(1997)
Top. Curr. Chem
, vol.185
, pp. 141-173
-
-
Nédélec, J.-Y.1
Périchon, J.2
Troupel, M.3
-
29
-
-
28744437194
-
Efficient N-p-methoxyphenyl amine deprotection through anodic oxidation
-
DOI 10.1021/jo051867o
-
De Lamo Marin, S.; Martens, T.; Mioskowski, C. Royer, J. Efficient N-p-methoxyphenyl amine deprotection through anodic oxidation. J. Org. Chem. 2005, 70, 10592-10595. (Pubitemid 41759940)
-
(2005)
Journal of Organic Chemistry
, vol.70
, Issue.25
, pp. 10592-10595
-
-
De Marin, S.L.1
Martens, T.2
Mioskowski, C.3
Royer, J.4
-
30
-
-
0000418155
-
Electrochimie de complexes du nickel associés à la 22'-bipyridine dans le solvant N-méthylpyrrolidinone
-
Troupel, M.; Rollin, Y.; Sock, O.; Meyer, G.; Périchon, J. Electrochimie de complexes du nickel associés à la 2,2'-bipyridine dans le solvant N-méthylpyrrolidinone. New J. Chem. 1986, 10, 593-599.
-
(1986)
New J. Chem
, vol.10
, pp. 593-599
-
-
Troupel, M.1
Rollin, Y.2
Sock, O.3
Meyer, G.4
Périchon, J.5
-
31
-
-
33748463567
-
Efficient microwave-assisted synthesis of highly functionalized pyrimidine derivatives
-
DOI 10.1016/j.tet.2006.08.065, PII S0040402006013512
-
Hartung, C.G.; Backes, A.C.; Felber, B.; Missioy, A.; Philipp, A. Efficient microwave-assisted synthesis of highly functionalized pyrimidine derivatives. Tetrahedron 2006, 62, 10055-10064. (Pubitemid 44349152)
-
(2006)
Tetrahedron
, vol.62
, Issue.43
, pp. 10055-10064
-
-
Hartung, C.G.1
Backes, A.C.2
Felber, B.3
Missio, A.4
Philipp, A.5
|