-
1
-
-
53749084486
-
Recent advances in the chemistry of indazoles
-
Schmidt, A.; Beutler, A.; Snovydovych, B. Recent advances in the chemistry of indazoles. Eur. J. Org. Chem. 2008, 24, 4073-4095.
-
(2008)
Eur. J. Org. Chem
, vol.24
, pp. 4073-4095
-
-
Schmidt, A.1
Beutler, A.2
Snovydovych, B.3
-
2
-
-
0034684496
-
First combined selective N-and Carylations with boronic acids: Application to the synthesis of 1,3-diarylindazoles
-
Collot, V.; Bovy, P. R.; Rault, S. First combined selective N-and Carylations with boronic acids: application to the synthesis of 1,3-diarylindazoles. Tetrahedron Lett. 2000, 41, 9053-9057.
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 9053-9057
-
-
Collot, V.1
Bovy, P.R.2
Rault, S.3
-
3
-
-
0001688262
-
An improved synthesis of YC-1
-
Gordon, D. W. An improved synthesis of YC-1. Synlett 1998, 10, 1065-1066.
-
(1998)
Synlett
, vol.10
, pp. 1065-1066
-
-
Gordon, D.W.1
-
4
-
-
0026737691
-
A novel synthesis of 3-substituted indazole derivatives
-
Welch, W. M.; Hanau, C. E.; Whalen, W. M. A novel synthesis of 3-substituted indazole derivatives. Synthesis 1992, 10, 937-939.
-
(1992)
Synthesis
, vol.10
, pp. 937-939
-
-
Welch, W.M.1
Hanau, C.E.2
Whalen, W.M.3
-
5
-
-
0037041340
-
Sonogashira cross-coupling reaction of 3-iodoindazoles with various terminal alkynes: A mild and flexible strategy to design 2-aza tryptamines
-
Amautu, A.; Collot, V.; Ros, J. C.; Alayrac, C.; Witulski, B.; Rault, S. Sonogashira cross-coupling reaction of 3-iodoindazoles with various terminal alkynes: a mild and flexible strategy to design 2-aza tryptamines. Tetrahedron Lett. 2002, 43, 2695-2697.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 2695-2697
-
-
Amautu, A.1
Collot, V.2
Ros, J.C.3
Alayrac, C.4
Witulski, B.5
Rault, S.6
-
6
-
-
0034621966
-
Heck cross-coupling reaction of 3-iodoindazoles with methyl acrylate: A mild and flexible strategy to design 2-aza tryptamines
-
Collot, V.; Varlet, D.; Rault, S. Heck cross-coupling reaction of 3-iodoindazoles with methyl acrylate: a mild and flexible strategy to design 2-aza tryptamines. Tetrahedron Lett. 2000, 41, 4363-4366.
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 4363-4366
-
-
Collot, V.1
Varlet, D.2
Rault, S.3
-
7
-
-
78649794334
-
Efficient synthesis of new 3-heteroaryl-1-functionalized 1Hindazoles
-
Fraile, A.; Martín, M. R.; García Ruano, J-L.; Díaz, JA.; Arranz, E. Efficient synthesis of new 3-heteroaryl-1-functionalized 1Hindazoles. Tetrahedron 2011, 67, 100-105.
-
(2011)
Tetrahedron
, vol.67
, pp. 100-105
-
-
Fraile, A.1
Martín, M.R.2
García Ruano, J.-L.3
Díaz, J.A.4
Arranz, E.5
-
8
-
-
45749095896
-
1-[(Imidazolidin-2-yl)imino]indazole. Highly _2/I1 selective agonist: Synthesis, X-ray structure, and biological activity
-
Some recent publications on biological applications of substituted indazoles
-
Some recent publications on biological applications of substituted indazoles: Saczewski, F.; Kornicka, A.; Rybczynska, A.; Hudson, A. L.; Sean Miao, S.; Gdaniec, M.; Boblewski, K.; Lehmann, A. 1-[(Imidazolidin-2-yl)imino]indazole. Highly _2/I1 selective agonist: Synthesis, X-ray structure, and biological activity. J. Med. Chem. 2008, 51, 3599-3606.
-
(2008)
J. Med. Chem
, vol.51
, pp. 3599-3606
-
-
Saczewski, F.1
Kornicka, A.2
Rybczynska, A.3
Hudson, A.L.4
Sean Miao, S.5
Gdaniec, M.6
Boblewski, K.7
Lehmann, A.8
-
9
-
-
64349086788
-
Novel Indazole Non-Nucleoside Reverse Transcriptase Inhibitors Using Molecular Hybridization Based on Crystallographic Overlays
-
Jones, L. H.; Allan, G.; Barba, O.; Burt, C.; Corbau, R.; Dupont, T.; Knöchel, T.; Irving, S.; Middleton, D. S.; Mowbray, C. E.; Perros, M.; Ringrose, H.; Swain, N.A.; Webster, R.; Westby, M.; Phillips, C. Novel Indazole Non-Nucleoside Reverse Transcriptase Inhibitors Using Molecular Hybridization Based on Crystallographic Overlays. J. Med. Chem. 2009, 52, 1219-1223.
-
(2009)
J. Med. Chem
, vol.52
, pp. 1219-1223
-
-
Jones, L.H.1
Allan, G.2
Barba, O.3
Burt, C.4
Corbau, R.5
Dupont, T.6
Knöchel, T.7
Irving, S.8
Middleton, D.S.9
Mowbray, C.E.10
Perros, M.11
Ringrose, H.12
Swain, N.A.13
Webster, R.14
Westby, M.15
Phillips, C.16
-
10
-
-
56749177320
-
Indazole-based liver X receptor (LXR) modulators with maintained atherosclerotic lesion reduction activity but diminished stimulation of hepatic triglyceride synthesis
-
Wrobel, J.; Steffan, R.; Bowen, S. M.; Magolda, R.; Matelan, E.; Unwalla, R.; Basso, M.; Clerin, V.; Gardell, S. J.; Nambi, P.; Quinet, E.; Reminick, J. I.; Vlasuk, G. P.; Wang, S.; Feingold, I.; Huselton, C.; Bonn, T.; Farnegardh, M.; Hansson, T.; Nilsson, A. G.; Wilhelmsson, A.; Zamaratski, E.; Evans, M. J. Indazole-based liver X receptor (LXR) modulators with maintained atherosclerotic lesion reduction activity but diminished stimulation of hepatic triglyceride synthesis. J. Med. Chem. 2008, 51, 7161-7168.
-
(2008)
J. Med. Chem
, vol.51
, pp. 7161-7168
-
-
Wrobel, J.1
Steffan, R.2
Bowen, S.M.3
Magolda, R.4
Matelan, E.5
Unwalla, R.6
Basso, M.7
Clerin, V.8
Gardell, S.J.9
Nambi, P.10
Quinet, E.11
Reminick, J.I.12
Vlasuk, G.P.13
Wang, S.14
Feingold, I.15
Huselton, C.16
Bonn, T.17
Farnegardh, M.18
Hansson, T.19
Nilsson, A.G.20
Wilhelmsson, A.21
Zamaratski, E.22
Evans, M.J.23
more..
-
11
-
-
78649815516
-
Design, synthesis, and structure_activity relationships of 3-ethynyl-1H-indazoles as inhibitors of the phosphatidylinositol 3-kinase signaling pathway
-
Barile, E.; De, S. K.; Carlson, C. B.; Chen, V.; Knutzen, C.; Riel-Mehan, M.; Yang, L.; Dahl, R.; Chiang, G.; Pellecchia, M.; Design, synthesis, and structure_activity relationships of 3-ethynyl-1H-indazoles as inhibitors of the phosphatidylinositol 3-kinase signaling pathway. J. Med. Chem. 2010, 53, 8368-8375.
-
(2010)
J. Med. Chem
, vol.53
, pp. 8368-8375
-
-
Barile, E.1
De, S.K.2
Carlson, C.B.3
Chen, V.4
Knutzen, C.5
Riel-Mehan, M.6
Yang, L.7
Dahl, R.8
Chiang, G.9
Pellecchia, M.10
-
12
-
-
23244451883
-
Synthesis of 4-substituted and 3, 4-disubstituted indazole derivatives by palladium crosscoupling reactions
-
El Kazzouli, S.; Bouissane, L.; Khouili, M.; Guillaumet, G. Synthesis of 4-substituted and 3, 4-disubstituted indazole derivatives by palladium crosscoupling reactions. Tetrahedron Lett. 2005, 46, 6163-6167.
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 6163-6167
-
-
El Kazzouli, S.1
Bouissane, L.2
Khouili, M.3
Guillaumet, G.4
-
13
-
-
84870601851
-
Direct C3-arylations of 1H-indazoles
-
Benyahia, A. Naas, M. El Kazzouli, S.; Essassi, EM. Guillaumet, G. Direct C3-arylations of 1H-indazoles. Eur. J. Org. Chem. 2012, 2012, 36, 7075-7081.
-
(2012)
Eur. J. Org. Chem
, vol.2012
, Issue.36
, pp. 7075-7081
-
-
Benyahia, A.1
Naas, M.2
El Kazzouli, S.3
Essassi, E.M.4
Guillaumet, G.5
-
14
-
-
22544486271
-
New and efficient synthesis of bi-and trisubstituted indazoles
-
Bouissane, L.; El Kazzouli, S.; Rakib, E.M.; Khouili, M.; Guillaumet, G. New and efficient synthesis of bi-and trisubstituted indazoles. Tetrahedron 2005, 61, 8218-8225.
-
(2005)
Tetrahedron
, vol.61
, pp. 8218-8225
-
-
Bouissane, L.1
El Kazzouli, S.2
Rakib, E.M.3
Khouili, M.4
Guillaumet, G.5
-
15
-
-
30344440110
-
Synthesis and biological evaluation of N-(7-indazolyl)benzenesulfonamide derivatives as potent cell cycle inhibitors
-
Bouissane, L.; El Kazzouli, S.; Léonce, S.; Pfeiffer, B.; Rakib, E.M.; Khouili, M.; Guillaumet, G. Synthesis and biological evaluation of N-(7-indazolyl)benzenesulfonamide derivatives as potent cell cycle inhibitors. Bioorg. Med. Chem. 2006, 14, 1078-1088.
-
(2006)
Bioorg. Med. Chem
, vol.14
, pp. 1078-1088
-
-
Bouissane, L.1
El Kazzouli, S.2
Léonce, S.3
Pfeiffer, B.4
Rakib, E.M.5
Khouili, M.6
Guillaumet, G.7
-
16
-
-
77954315944
-
Synthesis of 1,3-diarylsubstituted indazoles utilizing a Suzuki cross-coupling/deprotection/Narylation sequence
-
Salovich, J. M.; Lindsley, C. W.; Hopkins, C. R. Synthesis of 1,3-diarylsubstituted indazoles utilizing a Suzuki cross-coupling/deprotection/Narylation sequence Tetrahedron Lett., 2010, 51, 3796-3799.
-
(2010)
Tetrahedron Lett
, vol.51
, pp. 3796-3799
-
-
Salovich, J.M.1
Lindsley, C.W.2
Hopkins, C.R.3
-
17
-
-
34848907405
-
Synthesis of polysubstitued imidazo[1,2-a]pyridines via microwave-assisted one-pot cyclization/Suzuki coupling/palladium-catalyzed heteroarylation
-
For publications on Suzuki-Miyaura cross-coupling see
-
For publications on Suzuki-Miyaura cross-coupling see: Koubachi, J.; El Kazzouli, S.; Berteina-Raboin, S.; Mouaddib, A.; Guillaumet, G. Synthesis of polysubstitued imidazo[1,2-a]pyridines via microwave-assisted one-pot cyclization/Suzuki coupling/palladium-catalyzed heteroarylation. J. Org. Chem. 2007, 72, 7650-7655.
-
(2007)
J. Org. Chem
, vol.72
, pp. 7650-7655
-
-
Koubachi, J.1
El Kazzouli, S.2
Berteina-Raboin, S.3
Mouaddib, A.4
Guillaumet, G.5
-
18
-
-
36949028304
-
Supported synthesis and functionnalization of 2'-deoxyuridine by Suzuki-Miyaura cross-coupling
-
El Kazzouli, S.; Berteina-Raboin, S.; Agrofoglio, L. Supported synthesis and functionnalization of 2'-deoxyuridine by Suzuki-Miyaura cross-coupling. Nucleosides, Nucleotides Nucleic Acids 2007, 26, 1395-1398.
-
(2007)
Nucleosides, Nucleotides Nucleic Acids
, vol.26
, pp. 1395-1398
-
-
El Kazzouli, S.1
Berteina-Raboin, S.2
Agrofoglio, L.3
-
19
-
-
77957698670
-
A new palladium precatalyst allows for the fast Suzuki_Miyaura coupling reactions of unstable polyfluorophenyl and 2-heteroaryl boronic Acids
-
Kinzel, T.; Zhang, Y.; Buchwald, S. L. A new palladium precatalyst allows for the fast Suzuki_Miyaura coupling reactions of unstable polyfluorophenyl and 2-heteroaryl boronic Acids. J. Am. Chem. Soc. 2010, 132, 14073-14073.
-
(2010)
J. Am. Chem. Soc
, vol.132
, pp. 14073
-
-
Kinzel, T.1
Zhang, Y.2
Buchwald, S.L.3
-
20
-
-
77955156824
-
A modular sydnone cycloaddition/ Suzuki-Miyaura cross-coupling strategy to unsymmetrical 3,5-bis(hetero)aromatic pyrazoles
-
Delaunay, T.; Genix, P.; Es-Sayed, M.; Vors, JP.; Monteiro, N.; Balme, G. A modular sydnone cycloaddition/ Suzuki-Miyaura cross-coupling strategy to unsymmetrical 3,5-bis(hetero)aromatic pyrazoles. Org. Lett. 2010, 12, 3328-3331.
-
(2010)
Org. Lett
, vol.12
, pp. 3328-3331
-
-
Delaunay, T.1
Genix, P.2
Es-Sayed, M.3
Vors, J.P.4
Monteiro, N.5
Balme, G.6
-
22
-
-
0033612127
-
Suzuki-type cross-coupling reaction of 3-iodoindazoles with aryl boronic acids: A general and flexible route to 3-arylindazoles
-
Collot, V.; Dallemagne, P.; Bovy, P. R.; Rault, S. Suzuki-type cross-coupling reaction of 3-iodoindazoles with aryl boronic acids: A general and flexible route to 3-arylindazoles; Tetrahedron 1999, 55, 6917-6917.
-
(1999)
Tetrahedron
, vol.55
, pp. 6917
-
-
Collot, V.1
Dallemagne, P.2
Bovy, P.R.3
Rault, S.4
-
23
-
-
84555188469
-
Design, synthesis and biological evaluation of trypanosoma brucei trypanothione synthetase inhibitors
-
Spinks, D.; Torrie, L.S.; Thompson, S.; Harrison, J.R.; Frearson, J.A.; Read, K.D.; Fairlamb, A.H.; Wyatt, P.G.; Gilbert, I.H. Design, synthesis and biological evaluation of trypanosoma brucei trypanothione synthetase inhibitors. ChemMedChem. 2012, 7, 95-106.
-
(2012)
ChemMedChem
, vol.7
, pp. 95-106
-
-
Spinks, D.1
Torrie, L.S.2
Thompson, S.3
Harrison, J.R.4
Frearson, J.A.5
Read, K.D.6
Fairlamb, A.H.7
Wyatt, P.G.8
Gilbert, I.H.9
-
24
-
-
33750529730
-
3-(Indol-2-yl)indazoles as chek1 kinase inhibitors: Optimization of potency and selectivity via substitution at C6
-
Fraley, M. E.; Steen, J. T.; Brnardic, E. J.; Arrington, K. L.; Spencer, K. L.; Hanney, B. A.; Kim, Y.; Hartman, G. D.; Stirdivant, S. M.; Drakas, B. A. Rickert, K.; Walsh, E. S.; Hamilton, K.; Buser, C. A.; Hardwick, J.; Tao, W.; Beck, S.C.; Mao, X.; Lobell, R. B.; Sepp-Lorenzino, L.; Yan, Y.; Ikuta, M.; Munshi, S. K.; Kuoc, L. C.; Kreatsoulas, C. 3-(Indol-2-yl)indazoles as chek1 kinase inhibitors: Optimization of potency and selectivity via substitution at C6 Bioorg. Med. Chem. Lett. 2006, 16, 6049-6053.
-
(2006)
Bioorg. Med. Chem. Lett
, vol.16
, pp. 6049-6053
-
-
Fraley, M.E.1
Steen, J.T.2
Brnardic, E.J.3
Arrington, K.L.4
Spencer, K.L.5
Hanney, B.A.6
Kim, Y.7
Hartman, G.D.8
Stirdivant, S.M.9
Drakas, B.A.10
Rickert, K.11
Walsh, E.S.12
Hamilton, K.13
Buser, C.A.14
Hardwick, J.15
Tao, W.16
Beck, S.C.17
Mao, X.18
Lobell, R.B.19
Sepp-Lorenzino, L.20
Yan, Y.21
Ikuta, M.22
Munshi, S.K.23
Kuoc, L.C.24
Kreatsoulas, C.25
more..
-
25
-
-
33744790585
-
Efficient and simple synthesis of 3-aryl-1H-pyrazoles
-
Gérard, A-L.; Bouillon, A.; Mahatsekake, C.; Collota, V.; Rault, S. Efficient and simple synthesis of 3-aryl-1H-pyrazoles. Tetrahedron Lett. 2006, 47, 4665-4669.
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 4665-4669
-
-
Gérard, A.-L.1
Bouillon, A.2
Mahatsekake, C.3
Collota, V.4
Rault, S.5
-
26
-
-
80054782808
-
Design, synthesis and insight into the structure-activity relationship of 1,3-disubstituted indazoles as novel HIF-1 inhibitors
-
An, H.; Kim, N-J.; Jung, J-W.; Jang, H.; Park, J-W.; Suh, Y-G. Design, synthesis and insight into the structure-activity relationship of 1,3-disubstituted indazoles as novel HIF-1 inhibitors Bioorg. Med. Chem. Lett. 2011, 21, 6297-6300.
-
(2011)
Bioorg. Med. Chem. Lett
, vol.21
, pp. 6297-6300
-
-
An, H.1
Kim, N.-J.2
Jung, J.-W.3
Jang, H.4
Park, J.-W.5
Suh, Y.-G.6
-
27
-
-
72049120102
-
2,4-Diaminopyrimidine MK2 inhibitors. Part II: Structure-based inhibitor optimization
-
Harris, C. M.; Ericsson, A. M.; Argiriadi, M. A.; Barberis, C.; Borhani, D. W.; Burchat, A.; Calderwood, D. J.; Cunha, G. A.; Dixon, R. W.; Frank, K. E.; Johnson, E. F.; Kamens, J.; Kwak, S.; Li, B.; Mullen, K. D.; Perron, D. C.; Wang, L.; Wishart, N.; Wu, X.; Zhang, X.; Zmetra, T. R.; Talanian, R. V. 2,4-Diaminopyrimidine MK2 inhibitors. Part II: Structure-based inhibitor optimization Bioorg. Med. Chem. Lett. 2010, 20, 334-337.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, pp. 334-337
-
-
Harris, C.M.1
Ericsson, A.M.2
Argiriadi, M.A.3
Barberis, C.4
Borhani, D.W.5
Burchat, A.6
Calderwood, D.J.7
Cunha, G.A.8
Dixon, R.W.9
Frank, K.E.10
Johnson, E.F.11
Kamens, J.12
Kwak, S.13
Li, B.14
Mullen, K.D.15
Perron, D.C.16
Wang, L.17
Wishart, N.18
Wu, X.19
Zhang, X.20
Zmetra, T.R.21
Talanian, R.V.22
more..
-
28
-
-
58149355914
-
Efficient and scalable synthesis of 3,5,7-trisubstituted 1Hindazoles as potent IKK2 inhibitors
-
Lin, X.; Busch-Peterson, J.; Deng, J.; Edwards, C.; Zang, Z.; Kerns, J. K. Efficient and scalable synthesis of 3,5,7-trisubstituted 1Hindazoles as potent IKK2 inhibitors. Synlett, 2008, 20, 3216-3216.
-
(2008)
Synlett
, vol.20
, pp. 3216
-
-
Lin, X.1
Busch-Peterson, J.2
Deng, J.3
Edwards, C.4
Zang, Z.5
Kerns, J.K.6
-
29
-
-
85196433524
-
Preparation of indazole derivatives as JNK enzyme inhibitors US Patent
-
01 Jul
-
Bhagwat, S. S.; Satoh, Y.; Sakata, S. T.; Buhr, C. A.; Albers, R.; Sapienza, J.; Plantevin, V.; Chao, Q.; Sahasrabudhe, K.; Ferri, R. Preparation of indazole derivatives as JNK enzyme inhibitors US Patent, Appl. Publ., 20040127536, 01 Jul 2004.
-
(2004)
Appl. Publ
, pp. 20040127536
-
-
Bhagwat, S.S.1
Satoh, Y.2
Sakata, S.T.3
Buhr, C.A.4
Albers, R.5
Sapienza, J.6
Plantevin, V.7
Chao, Q.8
Sahasrabudhe, K.9
Ferri, R.10
-
30
-
-
0038607286
-
Product class 2: 1H-and 2H-indazoles
-
Stadlbauer, W. Product class 2: 1H-and 2H-indazoles. Sci. Synth. 2002, 12, 227-340.
-
(2002)
Sci. Synth
, vol.12
, pp. 227-340
-
-
Stadlbauer, W.1
-
31
-
-
0001611428
-
Phase transfer catalyzed synthesis of indazoles from o-alkylbenzenediazonium tetrafluoroborates
-
Bartsch, R. A.; Yang, I-W. Phase transfer catalyzed synthesis of indazoles from o-alkylbenzenediazonium tetrafluoroborates. J. Heterocyclic Chem. 1984, 20, 1063-1064.
-
(1984)
J. Heterocyclic Chem
, vol.20
, pp. 1063-1064
-
-
Bartsch, R.A.1
Yang, I.-W.2
-
32
-
-
84980123949
-
Ueber Bildung von Indazolen aus nitrirten orthomethylirten Aminen
-
Noelting, E. Ueber Bildung von Indazolen aus nitrirten orthomethylirten Aminen. Berichte 1904, 37, 2556-2597.
-
(1904)
Berichte
, vol.37
, pp. 2556-2597
-
-
Noelting, E.1
-
33
-
-
84864995412
-
New hypotheses for the binding mode of 4-and 7-substituted indazoles in the active site of neuronal nitric oxide synthase
-
Lohou, E.; Sopkova-de Oliveira Santos, J.; Schumann-Bard, P.; Boulouard, M.; Stiebing, S.; Rault, S.; Collot, V. New hypotheses for the binding mode of 4-and 7-substituted indazoles in the active site of neuronal nitric oxide synthase Bioorg. Med. Chem. 2012, 20, 5296-5304.
-
(2012)
Bioorg. Med. Chem
, vol.20
, pp. 5296-5304
-
-
Lohou, E.1
Sopkova-De Oliveira Santos, J.2
Schumann-Bard, P.3
Boulouard, M.4
Stiebing, S.5
Rault, S.6
Collot, V.7
-
34
-
-
44449090492
-
Inhibitory effects of a series of 7-substituted-indazoles toward nitric oxide synthases: Particular potency of 1H-indazole-7-carbonitrile
-
Cottyn, B.; Acher, F.; Ramassamy, B.; Alvey, L.; Lepoivre, M.; Frapart, Y.; Stuehr, D.; Mansuy, D.; Boucher, J-L.; Vichard, D. Inhibitory effects of a series of 7-substituted-indazoles toward nitric oxide synthases: Particular potency of 1H-indazole-7-carbonitrile. Bioorg. Med. Chem. 2008, 16, 5962-5973.
-
(2008)
Bioorg. Med. Chem
, vol.16
, pp. 5962-5973
-
-
Cottyn, B.1
Acher, F.2
Ramassamy, B.3
Alvey, L.4
Lepoivre, M.5
Frapart, Y.6
Stuehr, D.7
Mansuy, D.8
Boucher, J.-L.9
Vichard, D.10
|