-
1
-
-
70350755331
-
-
Fojo, T. Humana Press: Totowa, NJ
-
Jordan, M.; Wilson, L. In The Role of Microtubules in Cell Biology, Neurobiology, and Oncology; Fojo, T., Ed.; Humana Press: Totowa, NJ, 2008; p 47-81.
-
(2008)
The Role of Microtubules in Cell Biology, Neurobiology, and Oncology
, pp. 47-81
-
-
Jordan, M.1
Wilson, L.2
-
2
-
-
70350755331
-
-
Fojo, T. Humana Press: Totowa, NJ
-
Giavazzi, R.; Bonezzi, K.; Taraboletti, G. In The Role of Microtubules in Cell Biology, Neurobiology, and Oncology; Fojo, T., Ed.; Humana Press: Totowa, NJ, 2008; p 519-530.
-
(2008)
The Role of Microtubules in Cell Biology, Neurobiology, and Oncology
, pp. 519-530
-
-
Giavazzi, R.1
Bonezzi, K.2
Taraboletti, G.3
-
3
-
-
1942438028
-
Microtubules as a target for anticancer drugs
-
Jordan, M. A.; Wilson, L. Microtubules as a target for anticancer drugs Nat. Rev. Cancer 2004, 4, 253-265
-
(2004)
Nat. Rev. Cancer
, vol.4
, pp. 253-265
-
-
Jordan, M.A.1
Wilson, L.2
-
4
-
-
77955289715
-
-
Leslie, W. John, J. C. Academic Press: Burlington, MA, Vol. Vol
-
Cormier, A.; Knossow, M.; Wang, C.; Gigant, B. In Methods in Cell Biology; Leslie, W.; John, J. C., Eds.; Academic Press: Burlington, MA, 2010; Vol. Vol. 95, p 373-390.
-
(2010)
Methods in Cell Biology
, vol.95
, pp. 373-390
-
-
Cormier, A.1
Knossow, M.2
Wang, C.3
Gigant, B.4
-
5
-
-
0035942226
-
The binding conformation of Taxol in I-tubulin: A model based on electron crystallographic density
-
Snyder, J. P.; Nettles, J. H.; Cornett, B.; Downing, K. H.; Nogales, E. The binding conformation of Taxol in I-tubulin: A model based on electron crystallographic density Proc. Natl. Acad. Sci. U.S.A. 2001, 98, 5312-5316
-
(2001)
Proc. Natl. Acad. Sci. U.S.A.
, vol.98
, pp. 5312-5316
-
-
Snyder, J.P.1
Nettles, J.H.2
Cornett, B.3
Downing, K.H.4
Nogales, E.5
-
6
-
-
1642401199
-
Insight into tubulin regulation from a complex with colchicine and a stathmin-like domain
-
Ravelli, R. B. G.; Gigant, B.; Curmi, P. A.; Jourdain, I.; Lachkar, S.; Sobel, A.; Knossow, M. Insight into tubulin regulation from a complex with colchicine and a stathmin-like domain Nature 2004, 428, 198-202
-
(2004)
Nature
, vol.428
, pp. 198-202
-
-
Ravelli, R.B.G.1
Gigant, B.2
Curmi, P.A.3
Jourdain, I.4
Lachkar, S.5
Sobel, A.6
Knossow, M.7
-
7
-
-
0024513175
-
Isolation and structure of the strong cell growth and tubulin inhibitor combretastatin A-4
-
Pettit, G. R.; Singh, S. B.; Hamel, E.; Lin, C. M.; Alberts, D. S.; Garcia-Kendall, D. Isolation and structure of the strong cell growth and tubulin inhibitor combretastatin A-4 Experientia 1989, 45, 209-211
-
(1989)
Experientia
, vol.45
, pp. 209-211
-
-
Pettit, G.R.1
Singh, S.B.2
Hamel, E.3
Lin, C.M.4
Alberts, D.S.5
Garcia-Kendall, D.6
-
8
-
-
65549090459
-
A review and update of the current status of the vasculature-disabling agent combretastatin-A4 phosphate (CA4P)
-
Siemann, D. W.; Chaplin, D. J.; Walicke, P. A. A review and update of the current status of the vasculature-disabling agent combretastatin-A4 phosphate (CA4P) Expert Opin. Invest. Drugs 2009, 18, 189-197
-
(2009)
Expert Opin. Invest. Drugs
, vol.18
, pp. 189-197
-
-
Siemann, D.W.1
Chaplin, D.J.2
Walicke, P.A.3
-
9
-
-
84876727508
-
Design of combretastatin A-4 analogs as tubulin targeted vascular disrupting agent with special emphasis on their cis-restricted isomers
-
Rajak, H.; Kumar Dewangan, P.; Patel, V.; Kumar Jain, D.; Singh, A.; Veerasamy, R.; Chander Sharma, P.; Dixit, A. Design of combretastatin A-4 analogs as tubulin targeted vascular disrupting agent with special emphasis on their cis-restricted isomers Curr. Pharm. Des. 2013, 19, 1923-1955
-
(2013)
Curr. Pharm. Des.
, vol.19
, pp. 1923-1955
-
-
Rajak, H.1
Kumar Dewangan, P.2
Patel, V.3
Kumar Jain, D.4
Singh, A.5
Veerasamy, R.6
Chander Sharma, P.7
Dixit, A.8
-
10
-
-
33744820579
-
Medicinal chemistry of combretastatin A4: Present and future directions
-
Tron, G. C.; Pirali, T.; Sorba, G.; Pagliai, F.; Busacca, S.; Genazzani, A. A. Medicinal chemistry of combretastatin A4: Present and future directions J. Med. Chem. 2006, 49, 3033-3044
-
(2006)
J. Med. Chem.
, vol.49
, pp. 3033-3044
-
-
Tron, G.C.1
Pirali, T.2
Sorba, G.3
Pagliai, F.4
Busacca, S.5
Genazzani, A.A.6
-
11
-
-
34248159068
-
Small molecule vascular disrupting agents: Potential new drugs for cancer treatment
-
Cai, S. X. Small molecule vascular disrupting agents: Potential new drugs for cancer treatment Recent Pat. Anti-Cancer Drug Discovery 2007, 23, 79-101
-
(2007)
Recent Pat. Anti-Cancer Drug Discovery
, vol.23
, pp. 79-101
-
-
Cai, S.X.1
-
12
-
-
84862532904
-
Phase i trial of combretastatin A4 phosphate (CA4P) in combination with bevacizumab in patients with advanced cancer
-
Nathan, P.; Zweifel, M.; Padhani, A. R.; Koh, D.-M.; Ng, M.; Collins, D. J.; Harris, A.; Carden, C.; Smythe, J.; Fisher, N.; Taylor, N. J.; Stirling, J. J.; Lu, S.-P.; Leach, M. O.; Rustin, G. J. S.; Judson, I. Phase I trial of combretastatin A4 phosphate (CA4P) in combination with bevacizumab in patients with advanced cancer Clin. Cancer Res. 2012, 18, 3428-3439
-
(2012)
Clin. Cancer Res.
, vol.18
, pp. 3428-3439
-
-
Nathan, P.1
Zweifel, M.2
Padhani, A.R.3
Koh, D.-M.4
Ng, M.5
Collins, D.J.6
Harris, A.7
Carden, C.8
Smythe, J.9
Fisher, N.10
Taylor, N.J.11
Stirling, J.J.12
Lu, S.-P.13
Leach, M.O.14
Rustin, G.J.S.15
Judson, I.16
-
13
-
-
84899956978
-
A phase i pharmacokinetic study of the vascular disrupting agent ombrabulin (AVE8062) and docetaxel in advanced solid tumours
-
Eskens, F. A. L. M.; Tresca, P.; Tosi, D.; Van Doorn, L.; Fontaine, H.; Van der Gaast, A.; Veyrat-Follet, C.; Oprea, C.; Hospitel, M.; Dieras, V. A phase I pharmacokinetic study of the vascular disrupting agent ombrabulin (AVE8062) and docetaxel in advanced solid tumours Br. J. Cancer 2014, 110, 2170-2177
-
(2014)
Br. J. Cancer
, vol.110
, pp. 2170-2177
-
-
Eskens, F.A.L.M.1
Tresca, P.2
Tosi, D.3
Van Doorn, L.4
Fontaine, H.5
Van Der Gaast, A.6
Veyrat-Follet, C.7
Oprea, C.8
Hospitel, M.9
Dieras, V.10
-
14
-
-
77955550424
-
Expeditious synthesis of 1,1-diarylethylenes related to isocombretastatin A-4 (isoCA-4) via palladium-catalyzed arylation of N-tosylhydrazones with aryl triflates
-
Treguier, B.; Hamze, A.; Provot, O.; Brion, J. D.; Alami, M. Expeditious synthesis of 1,1-diarylethylenes related to isocombretastatin A-4 (isoCA-4) via palladium-catalyzed arylation of N-tosylhydrazones with aryl triflates Tetrahedron Lett. 2009, 50, 6549-6552
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 6549-6552
-
-
Treguier, B.1
Hamze, A.2
Provot, O.3
Brion, J.D.4
Alami, M.5
-
15
-
-
64549087206
-
Palladium-catalyzed Markovnikov terminal arylalkynes hydrostannation: Application to the synthesis of 1,1-diarylethylenes
-
Hamze, A.; Veau, D.; Provot, O.; Brion, J. D.; Alami, M. Palladium-catalyzed Markovnikov terminal arylalkynes hydrostannation: Application to the synthesis of 1,1-diarylethylenes J. Org. Chem. 2009, 74, 1337-1340
-
(2009)
J. Org. Chem.
, vol.74
, pp. 1337-1340
-
-
Hamze, A.1
Veau, D.2
Provot, O.3
Brion, J.D.4
Alami, M.5
-
16
-
-
77956570131
-
Pd-catalyzed reaction of sterically hindered hydrazones with aryl halides: Synthesis of tetra-substituted olefins related to iso-combretastatin A4
-
Brachet, E.; Hamze, A.; Peyrat, J. F.; Brion, J. D.; Alami, M. Pd-catalyzed reaction of sterically hindered hydrazones with aryl halides: Synthesis of tetra-substituted olefins related to iso-combretastatin A4 Org. Lett. 2010, 12, 4042-4045
-
(2010)
Org. Lett.
, vol.12
, pp. 4042-4045
-
-
Brachet, E.1
Hamze, A.2
Peyrat, J.F.3
Brion, J.D.4
Alami, M.5
-
17
-
-
44349096338
-
Synthesis and antitumor activity of benzils related to combretastatin A-4
-
Mousset, C.; Giraud, A.; Provot, O.; Hamze, A.; Bignon, J.; Liu, J. M.; Thoret, S.; Dubois, J.; Brion, J. D.; Alami, M. Synthesis and antitumor activity of benzils related to combretastatin A-4 Bioorg. Med. Chem. Lett. 2008, 18, 3266-3271
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 3266-3271
-
-
Mousset, C.1
Giraud, A.2
Provot, O.3
Hamze, A.4
Bignon, J.5
Liu, J.M.6
Thoret, S.7
Dubois, J.8
Brion, J.D.9
Alami, M.10
-
18
-
-
84860349179
-
Conformationnally restricted naphthalene derivatives type isocombretastatin A-4 and isoerianin analogues: Synthesis, cytotoxicity and antitubulin activity
-
Rasolofonjatovo, E.; Provot, O.; Hamze, A.; Rodrigo, J.; Bignon, J.; Wdzieczak-Bakala, J.; Desravines, D.; Dubois, J.; Brion, J.-D.; Alami, M. Conformationnally restricted naphthalene derivatives type isocombretastatin A-4 and isoerianin analogues: Synthesis, cytotoxicity and antitubulin activity Eur. J. Med. Chem. 2012, 52, 22-32
-
(2012)
Eur. J. Med. Chem.
, vol.52
, pp. 22-32
-
-
Rasolofonjatovo, E.1
Provot, O.2
Hamze, A.3
Rodrigo, J.4
Bignon, J.5
Wdzieczak-Bakala, J.6
Desravines, D.7
Dubois, J.8
Brion, J.-D.9
Alami, M.10
-
19
-
-
79952165575
-
Discovery of isoerianin analogues as promising anticancer agents
-
Messaoudi, S.; Hamze, A.; Provot, O.; Treguier, B.; De Losada, J. R.; Bignon, J.; Liu, J. M.; Wdzieczak-Bakala, J.; Thoret, S.; Dubois, J.; Brion, J. D.; Alami, M. Discovery of isoerianin analogues as promising anticancer agents ChemMedChem. 2011, 6, 488-497
-
(2011)
ChemMedChem.
, vol.6
, pp. 488-497
-
-
Messaoudi, S.1
Hamze, A.2
Provot, O.3
Treguier, B.4
De Losada, J.R.5
Bignon, J.6
Liu, J.M.7
Wdzieczak-Bakala, J.8
Thoret, S.9
Dubois, J.10
Brion, J.D.11
Alami, M.12
-
20
-
-
67650760201
-
Isocombretastatins A versus combretastatins A: The forgotten isoCA-4 isomer as a highly promising cytotoxic and antitubulin agent
-
Messaoudi, S.; Tréguier, B.; Hamze, A.; Provot, O.; Peyrat, J.-F.; De Losada, J. R.; Liu, J.-M.; Bignon, J.; Wdzieczak-Bakala, J.; Thoret, S.; Dubois, J.; Brion, J.-D.; Alami, M. Isocombretastatins A versus combretastatins A: The forgotten isoCA-4 isomer as a highly promising cytotoxic and antitubulin agent J. Med. Chem. 2009, 52, 4538-4542
-
(2009)
J. Med. Chem.
, vol.52
, pp. 4538-4542
-
-
Messaoudi, S.1
Tréguier, B.2
Hamze, A.3
Provot, O.4
Peyrat, J.-F.5
De Losada, J.R.6
Liu, J.-M.7
Bignon, J.8
Wdzieczak-Bakala, J.9
Thoret, S.10
Dubois, J.11
Brion, J.-D.12
Alami, M.13
-
21
-
-
73449087663
-
Synthesis, biological evaluation of 1,1-diarylethylenes as a novel class of antimitotic agents
-
Hamze, A.; Giraud, A.; Messaoudi, S.; Provot, O.; Peyrat, J.-F.; Bignon, J.; Liu, J.-M.; Wdzieczak-Bakala, J.; Thoret, S.; Dubois, J.; Brion, J.-D.; Alami, M. Synthesis, biological evaluation of 1,1-diarylethylenes as a novel class of antimitotic agents ChemMedChem. 2009, 4, 1912-1924
-
(2009)
ChemMedChem.
, vol.4
, pp. 1912-1924
-
-
Hamze, A.1
Giraud, A.2
Messaoudi, S.3
Provot, O.4
Peyrat, J.-F.5
Bignon, J.6
Liu, J.-M.7
Wdzieczak-Bakala, J.8
Thoret, S.9
Dubois, J.10
Brion, J.-D.11
Alami, M.12
-
22
-
-
84877745532
-
An efficient coupling of N -tosylhydrazones with 2-halopyridines: Synthesis of 2-alpha-styrylpyridines endowed with antitumor activity
-
Lawson, M.; Hamze, A.; Peyrat, J. F.; Bignon, J.; Dubois, J.; Brion, J. D.; Alami, M. An efficient coupling of N -tosylhydrazones with 2-halopyridines: Synthesis of 2-alpha-styrylpyridines endowed with antitumor activity Org. Biomol. Chem. 2013, 11, 3664-3673
-
(2013)
Org. Biomol. Chem.
, vol.11
, pp. 3664-3673
-
-
Lawson, M.1
Hamze, A.2
Peyrat, J.F.3
Bignon, J.4
Dubois, J.5
Brion, J.D.6
Alami, M.7
-
23
-
-
80051992087
-
Synthesis of 2-(1-phenylvinyl)benzofurans and 2-(1-phenylvinyl)indoles as antimitotic agents by a tandem palladium-assisted coupling-cyclization reaction between 1-phenylvinyl iodides and ortho-substituted arylalkynes
-
Tréguier, B.; Rasolofonjatovo, E.; Hamze, A.; Provot, O.; Wdzieczak-Bakala, J.; Dubois, J.; Brion, J.-D.; Alami, M. Synthesis of 2-(1-phenylvinyl)benzofurans and 2-(1-phenylvinyl)indoles as antimitotic agents by a tandem palladium-assisted coupling-cyclization reaction between 1-phenylvinyl iodides and ortho-substituted arylalkynes Eur. J. Org. Chem. 2011, 4868-4876
-
(2011)
Eur. J. Org. Chem.
, pp. 4868-4876
-
-
Tréguier, B.1
Rasolofonjatovo, E.2
Hamze, A.3
Provot, O.4
Wdzieczak-Bakala, J.5
Dubois, J.6
Brion, J.-D.7
Alami, M.8
-
24
-
-
0034611597
-
Novel benzofuran and benzothiophene biphenyls as inhibitors of protein tyrosine phosphatase 1B with antihyperglycemic properties
-
Malamas, M. S.; Sredy, J.; Moxham, C.; Katz, A.; Xu, W.; McDevitt, R.; Adebayo, F. O.; Sawicki, D. R.; Seestaller, L.; Sullivan, D.; Taylor, J. R. Novel benzofuran and benzothiophene biphenyls as inhibitors of protein tyrosine phosphatase 1B with antihyperglycemic properties J. Med. Chem. 2000, 43, 1293-1310
-
(2000)
J. Med. Chem.
, vol.43
, pp. 1293-1310
-
-
Malamas, M.S.1
Sredy, J.2
Moxham, C.3
Katz, A.4
Xu, W.5
McDevitt, R.6
Adebayo, F.O.7
Sawicki, D.R.8
Seestaller, L.9
Sullivan, D.10
Taylor, J.R.11
-
25
-
-
78449284865
-
Potent and selective 5-LO inhibitor bearing benzothiophene pharmacophore: Discovery of MK-5286
-
Li, L.; Berthelette, C.; Chateauneuf, A.; Ouellet, M.; Sturino, C. F.; Wang, Z. Potent and selective 5-LO inhibitor bearing benzothiophene pharmacophore: Discovery of MK-5286 Bioorg. Med. Chem. Lett. 2010, 20, 7440-7443
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 7440-7443
-
-
Li, L.1
Berthelette, C.2
Chateauneuf, A.3
Ouellet, M.4
Sturino, C.F.5
Wang, Z.6
-
26
-
-
77649195497
-
Studies of benzothiophene template as potent factor IXa (FIXa) inhibitors in thrombosis
-
Wang, S.; Beck, R.; Blench, T.; Burd, A.; Buxton, S.; Malic, M.; Ayele, T.; Shaikh, S.; Chahwala, S.; Chander, C.; Holland, R.; Merette, S.; Zhao, L.; Blackney, M.; Watts, A. Studies of benzothiophene template as potent factor IXa (FIXa) inhibitors in thrombosis J. Med. Chem. 2010, 53, 1465-1472
-
(2010)
J. Med. Chem.
, vol.53
, pp. 1465-1472
-
-
Wang, S.1
Beck, R.2
Blench, T.3
Burd, A.4
Buxton, S.5
Malic, M.6
Ayele, T.7
Shaikh, S.8
Chahwala, S.9
Chander, C.10
Holland, R.11
Merette, S.12
Zhao, L.13
Blackney, M.14
Watts, A.15
-
27
-
-
84862277249
-
Novel substituted benzothiophene and thienothiophene carboxanilides and quinolones: Synthesis, photochemical synthesis, DNA-binding properties, antitumor evaluation and 3D-derived QSAR analysis
-
Aleksici M.; Bertosa, B.; Nhili, R.; Uzelac, L.; Jarak, I.; Depauw, S.; David-Cordonnier, M.-H.; Kralj, M.; Tomici S.; Karminski-Zamola, G. Novel substituted benzothiophene and thienothiophene carboxanilides and quinolones: Synthesis, photochemical synthesis, DNA-binding properties, antitumor evaluation and 3D-derived QSAR analysis J. Med. Chem. 2012, 55, 5044-5060
-
(2012)
J. Med. Chem.
, vol.55
, pp. 5044-5060
-
-
Aleksic, M.1
Bertosa, B.2
Nhili, R.3
Uzelac, L.4
Jarak, I.5
Depauw, S.6
David-Cordonnier, M.-H.7
Kralj, M.8
Tomic, S.9
Karminski-Zamola, G.10
-
28
-
-
0033583499
-
A new anti-tubulin agent containing the benzo[b]thiophene ring system
-
Pinney, K. G.; Bounds, A. D.; Dingeman, K. M.; Mocharla, V. P.; Pettit, G. R.; Bai, R.; Hamel, E. A new anti-tubulin agent containing the benzo[b]thiophene ring system Bioorg. Med. Chem. Lett. 1999, 9, 1081-1086
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 1081-1086
-
-
Pinney, K.G.1
Bounds, A.D.2
Dingeman, K.M.3
Mocharla, V.P.4
Pettit, G.R.5
Bai, R.6
Hamel, E.7
-
29
-
-
0037155526
-
Synthesis of 2,3-disubstituted benzo[ b ]thiophenes via palladium-catalyzed coupling and electrophilic cyclization of terminal acetylenes
-
Yue, D.; Larock, R. C. Synthesis of 2,3-disubstituted benzo[ b ]thiophenes via palladium-catalyzed coupling and electrophilic cyclization of terminal acetylenes J. Org. Chem. 2002, 67, 1905-1909
-
(2002)
J. Org. Chem.
, vol.67
, pp. 1905-1909
-
-
Yue, D.1
Larock, R.C.2
-
30
-
-
33746309818
-
Gold-catalyzed intramolecular carbothiolation of alkynes: Synthesis of 2,3-disubstituted benzothiophenes from (α-alkoxy alkyl) (ortho -alkynyl phenyl) sulfides
-
Nakamura, I.; Sato, T.; Yamamoto, Y. Gold-catalyzed intramolecular carbothiolation of alkynes: Synthesis of 2,3-disubstituted benzothiophenes from (α-alkoxy alkyl) (ortho -alkynyl phenyl) sulfides Angew. Chem., Int. Ed. 2006, 45, 4473-4475
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 4473-4475
-
-
Nakamura, I.1
Sato, T.2
Yamamoto, Y.3
-
31
-
-
0035801759
-
The synthesis and tubulin binding activity of thiophene-based analogues of combretastatin A-4
-
Flynn, B. L.; Flynn, G. P.; Hamel, E.; Jung, M. K. The synthesis and tubulin binding activity of thiophene-based analogues of combretastatin A-4 Bioorg. Med. Chem. Lett. 2001, 11, 2341-2343
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 2341-2343
-
-
Flynn, B.L.1
Flynn, G.P.2
Hamel, E.3
Jung, M.K.4
-
32
-
-
0035826341
-
A novel palladium-mediated coupling approach to 2,3-disubstituted benzo[ b ]thiophenes and its application to the synthesis of tubulin binding agents
-
Flynn, B. L.; Verdier-Pinard, P.; Hamel, E. A novel palladium-mediated coupling approach to 2,3-disubstituted benzo[ b ]thiophenes and its application to the synthesis of tubulin binding agents Org. Lett. 2001, 3, 651-654
-
(2001)
Org. Lett.
, vol.3
, pp. 651-654
-
-
Flynn, B.L.1
Verdier-Pinard, P.2
Hamel, E.3
-
33
-
-
17744415875
-
Diamino benzo[ b ]thiophene derivatives as a novel class of active site directed thrombin inhibitors. 5. Potency, efficacy, and pharmacokinetic properties of modified C-3 side chain derivatives
-
Sall, D. J.; Bailey, D. L.; Bastian, J. A.; Buben, J. A.; Chirgadze, N. Y.; Clemens-Smith, A. C.; Denney, M. L.; Fisher, M. J.; Giera, D. D.; Gifford-Moore, D. S.; Harper, R. W.; Johnson, L. M.; Klimkowski, V. J.; Kohn, T. J.; Lin, H.-S.; McCowan, J. R.; Palkowitz, A. D.; Richett, M. E.; Smith, G. F.; Snyder, D. W.; Takeuchi, K.; Toth, J. E.; Zhang, M. Diamino benzo[ b ]thiophene derivatives as a novel class of active site directed thrombin inhibitors. 5. Potency, efficacy, and pharmacokinetic properties of modified C-3 side chain derivatives J. Med. Chem. 2000, 43, 649-663
-
(2000)
J. Med. Chem.
, vol.43
, pp. 649-663
-
-
Sall, D.J.1
Bailey, D.L.2
Bastian, J.A.3
Buben, J.A.4
Chirgadze, N.Y.5
Clemens-Smith, A.C.6
Denney, M.L.7
Fisher, M.J.8
Giera, D.D.9
Gifford-Moore, D.S.10
Harper, R.W.11
Johnson, L.M.12
Klimkowski, V.J.13
Kohn, T.J.14
Lin, H.-S.15
McCowan, J.R.16
Palkowitz, A.D.17
Richett, M.E.18
Smith, G.F.19
Snyder, D.W.20
Takeuchi, K.21
Toth, J.E.22
Zhang, M.23
more..
-
34
-
-
77955350744
-
MPHT-promoted bromocyclization of ortho-substituted arylalkynes: Application to the synthesis of 2-substituted 3-bromobenzofurans and -benzo[ b ]thiophenes
-
Jacubert, M.; Tikad, A.; Provot, O.; Hamze, A.; Brion, J.-D.; Alami, M. MPHT-promoted bromocyclization of ortho-substituted arylalkynes: Application to the synthesis of 2-substituted 3-bromobenzofurans and -benzo[ b ]thiophenes Eur. J. Org. Chem. 2010, 2010, 4492-4500
-
(2010)
Eur. J. Org. Chem.
, vol.2010
, pp. 4492-4500
-
-
Jacubert, M.1
Tikad, A.2
Provot, O.3
Hamze, A.4
Brion, J.-D.5
Alami, M.6
-
35
-
-
34547212241
-
N -Tosylhydrazones as reagents for cross-coupling reactions: A route to polysubstituted olefins
-
Barluenga, J.; Moriel, P.; Valdes, C.; Aznar, F. N -Tosylhydrazones as reagents for cross-coupling reactions: A route to polysubstituted olefins Angew. Chem., Int. Ed. 2007, 46, 5587-5590
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 5587-5590
-
-
Barluenga, J.1
Moriel, P.2
Valdes, C.3
Aznar, F.4
-
36
-
-
79961219090
-
Tosylhydrazones: New uses for classic reagents in palladium-catalyzed cross-coupling and metal-free reactions
-
For review on tosylhydrazones chemistry, see
-
For review on tosylhydrazones chemistry, see: Barluenga, J.; Valdés, C. Tosylhydrazones: New uses for classic reagents in palladium-catalyzed cross-coupling and metal-free reactions Angew. Chem., Int. Ed. 2011, 50, 7486-7500
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 7486-7500
-
-
Barluenga, J.1
Valdés, C.2
-
37
-
-
80655144655
-
N -Tosylhydrazones: Versatile reagents for metal-catalyzed and metal-free cross-coupling reactions
-
Shao, Z.; Zhang, H. N -Tosylhydrazones: Versatile reagents for metal-catalyzed and metal-free cross-coupling reactions Chem. Soc. Rev. 2012, 41, 560-572
-
(2012)
Chem. Soc. Rev.
, vol.41
, pp. 560-572
-
-
Shao, Z.1
Zhang, H.2
-
38
-
-
84871079763
-
Synthesis, biological evaluation, and structure-activity relationships of tri- and tetrasubstituted olefins related to isocombretastatin A-4 as new tubulin inhibitors
-
Aziz, J.; Brachet, E.; Hamze, A.; Peyrat, J.-F.; Bernadat, G.; Morvan, E.; Bignon, J.; Wdzieczak-Bakala, J.; Desravines, D.; Dubois, J.; Tueni, M.; Yassine, A.; Brion, J.-D.; Alami, M. Synthesis, biological evaluation, and structure-activity relationships of tri- and tetrasubstituted olefins related to isocombretastatin A-4 as new tubulin inhibitors Org. Biomol. Chem. 2013, 11, 430-442
-
(2013)
Org. Biomol. Chem.
, vol.11
, pp. 430-442
-
-
Aziz, J.1
Brachet, E.2
Hamze, A.3
Peyrat, J.-F.4
Bernadat, G.5
Morvan, E.6
Bignon, J.7
Wdzieczak-Bakala, J.8
Desravines, D.9
Dubois, J.10
Tueni, M.11
Yassine, A.12
Brion, J.-D.13
Alami, M.14
-
39
-
-
84883777681
-
2-N Bond formation via ligand-free Pd-catalyzed oxidative coupling reaction of N -tosylhydrazones and indole derivatives
-
2-N Bond formation via ligand-free Pd-catalyzed oxidative coupling reaction of N -tosylhydrazones and indole derivatives J. Org. Chem. 2013, 78, 8485-8495
-
(2013)
J. Org. Chem.
, vol.78
, pp. 8485-8495
-
-
Roche, M.1
Frison, G.2
Brion, J.-D.3
Provot, O.4
Hamze, A.5
Alami, M.6
-
40
-
-
84874070986
-
Catalytic three-component one-pot reaction of hydrazones, dihaloarenes, and amines
-
Roche, M.; Hamze, A.; Brion, J.-D.; Alami, M. Catalytic three-component one-pot reaction of hydrazones, dihaloarenes, and amines Org. Lett. 2013, 15, 148-151
-
(2013)
Org. Lett.
, vol.15
, pp. 148-151
-
-
Roche, M.1
Hamze, A.2
Brion, J.-D.3
Alami, M.4
-
41
-
-
84872580639
-
Synthesis of ortho/ortho-substituted 1,1-diarylethylenes through cross-coupling reactions of sterically encumbered hydrazones and aryl halides
-
Roche, M.; Hamze, A.; Provot, O.; Brion, J.-D.; Alami, M. Synthesis of ortho/ortho-substituted 1,1-diarylethylenes through cross-coupling reactions of sterically encumbered hydrazones and aryl halides J. Org. Chem. 2013, 78, 445-454
-
(2013)
J. Org. Chem.
, vol.78
, pp. 445-454
-
-
Roche, M.1
Hamze, A.2
Provot, O.3
Brion, J.-D.4
Alami, M.5
-
42
-
-
84884499589
-
3-N bond formation via reductive coupling of N -tosylhydrazones with anilines
-
3-N bond formation via reductive coupling of N -tosylhydrazones with anilines Adv. Synth. Catal. 2013, 355, 2417-2429
-
(2013)
Adv. Synth. Catal.
, vol.355
, pp. 2417-2429
-
-
Aziz, J.1
Brion, J.-D.2
Hamze, A.3
Alami, M.4
-
43
-
-
84888298330
-
Gold versus palladium: A regioselective cycloisomerization of aromatic enynes
-
Aziz, J.; Frison, G.; Le Menez, P.; Brion, J. D.; Hamze, A.; Alami, M. Gold versus palladium: A regioselective cycloisomerization of aromatic enynes Adv. Synth. Catal. 2013, 355, 3425-3436
-
(2013)
Adv. Synth. Catal.
, vol.355
, pp. 3425-3436
-
-
Aziz, J.1
Frison, G.2
Le Menez, P.3
Brion, J.D.4
Hamze, A.5
Alami, M.6
-
44
-
-
9644285669
-
A convenient synthesis of acetylenes: Catalytic substitutions of acetylenic hydrogen with bromoalkenes, iodoarenes and bromopyridines
-
Sonogashira, K.; Tohda, Y.; Hagihara, N. A convenient synthesis of acetylenes: Catalytic substitutions of acetylenic hydrogen with bromoalkenes, iodoarenes and bromopyridines Tetrahedron Lett. 1975, 16, 4467-4470
-
(1975)
Tetrahedron Lett.
, vol.16
, pp. 4467-4470
-
-
Sonogashira, K.1
Tohda, Y.2
Hagihara, N.3
-
45
-
-
0027378315
-
An efficient palladium-catalyzed reaction of vinyl and aryl halides or triflates with terminal alkynes
-
Alami, M.; Ferri, F.; Linstrumelle, G. An efficient palladium-catalyzed reaction of vinyl and aryl halides or triflates with terminal alkynes Tetrahedron Lett. 1993, 34, 6403-6406
-
(1993)
Tetrahedron Lett.
, vol.34
, pp. 6403-6406
-
-
Alami, M.1
Ferri, F.2
Linstrumelle, G.3
-
46
-
-
84989498349
-
A convenient synthesis of ethynylarenes and diethynylarenes
-
Takahashi, S.; Kuroyama, Y.; Sonogashira, K.; Hagihara, N. A convenient synthesis of ethynylarenes and diethynylarenes Synthesis 1980, 1980, 627-630
-
(1980)
Synthesis
, vol.1980
, pp. 627-630
-
-
Takahashi, S.1
Kuroyama, Y.2
Sonogashira, K.3
Hagihara, N.4
-
47
-
-
70349335573
-
Solution-phase parallel synthesis of a multi-substituted benzo[ b ]thiophene library
-
Cho, C.-H.; Neuenswander, B.; Lushington, G. H.; Larock, R. C. Solution-phase parallel synthesis of a multi-substituted benzo[ b ]thiophene library J. Comb. Chem. 2009, 11, 900-906
-
(2009)
J. Comb. Chem.
, vol.11
, pp. 900-906
-
-
Cho, C.-H.1
Neuenswander, B.2
Lushington, G.H.3
Larock, R.C.4
-
48
-
-
33747793704
-
The selective reaction of aryl halides with KOH: Synthesis of phenols, aromatic ethers, and benzofurans
-
Anderson, K. W.; Ikawa, T.; Tundel, R. E.; Buchwald, S. L. The selective reaction of aryl halides with KOH: Synthesis of phenols, aromatic ethers, and benzofurans J. Am. Chem. Soc. 2006, 128, 10694-10695
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 10694-10695
-
-
Anderson, K.W.1
Ikawa, T.2
Tundel, R.E.3
Buchwald, S.L.4
-
49
-
-
38349078209
-
One-pot hydrosilylation-protodesilylation of functionalized diarylalkynes: A highly selective access to Z-stilbenes. Application to the synthesis of combretastatin A-4
-
Giraud, A.; Provot, O.; Hamzé, A.; Brion, J.-D.; Alami, M. One-pot hydrosilylation-protodesilylation of functionalized diarylalkynes: A highly selective access to Z-stilbenes. Application to the synthesis of combretastatin A-4 Tetrahedron Lett. 2008, 49, 1107-1110
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 1107-1110
-
-
Giraud, A.1
Provot, O.2
Hamzé, A.3
Brion, J.-D.4
Alami, M.5
-
50
-
-
33947717991
-
The concise synthesis of chalcone, indanone and indenone analogues of combretastatin A4
-
Kerr, D. J.; Hamel, E.; Jung, M. K.; Flynn, B. L. The concise synthesis of chalcone, indanone and indenone analogues of combretastatin A4 Bioorg. Med. Chem. 2007, 15, 3290-3298
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 3290-3298
-
-
Kerr, D.J.1
Hamel, E.2
Jung, M.K.3
Flynn, B.L.4
-
51
-
-
24944515311
-
A common pharmacophore for a diverse set of colchicine site inhibitors using a structure-based approach
-
Nguyen, T. L.; McGrath, C.; Hermone, A. R.; Burnett, J. C.; Zaharevitz, D. W.; Day, B. W.; Wipf, P.; Hamel, E.; Gussio, R. A common pharmacophore for a diverse set of colchicine site inhibitors using a structure-based approach J. Med. Chem. 2005, 48, 6107-6116
-
(2005)
J. Med. Chem.
, vol.48
, pp. 6107-6116
-
-
Nguyen, T.L.1
McGrath, C.2
Hermone, A.R.3
Burnett, J.C.4
Zaharevitz, D.W.5
Day, B.W.6
Wipf, P.7
Hamel, E.8
Gussio, R.9
-
52
-
-
0001237322
-
Tosylhydrazone salt pyrolyses: Phenyldiazomethanes
-
Creary, X.; Tam, W. W.; Albizati, K. F.; Stevens, R. V. Tosylhydrazone salt pyrolyses: Phenyldiazomethanes Org. Synth. 1986, 64, 207
-
(1986)
Org. Synth.
, vol.64
, pp. 207
-
-
Creary, X.1
Tam, W.W.2
Albizati, K.F.3
Stevens, R.V.4
|