-
1
-
-
32344432249
-
New arylthioindoles: Potent inhibitors of tubulin polymerization. 2. structure-activity relationships and molecular modeling studies
-
De Martino, G.; Edler, M.C.; la Regina, R.; Coluccia, A.; Barbera, M.C.; Barrow, D.; Nicholson, R.I.; Chiosis, G.; Brancale, A.; Hamel, E.; et al. New arylthioindoles: Potent Inhibitors of tubulin polymerization. 2. Structure-activity relationships and molecular modeling studies. J. Med. Chem. 2006, 49, 947-954.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 947-954
-
-
De Martino, G.1
Edler, M.C.2
La Regina, R.3
Coluccia, A.4
Barbera, M.C.5
Barrow, D.6
Nicholson, R.I.7
Chiosis, G.8
Brancale, A.9
Hamel, E.10
-
2
-
-
33845199658
-
Inhibition of 5-lipoxygenase by mk886 augments the antitumor activity of celecoxib in human colon cancer cells
-
Cianchi, F.; Cortesini, C.; Magnelli, L.; Fanti, E.; Papucci, L.; Schiavone, N.; Messerini, L.; Vannacci, A.; Capaccioli, S.; Perna, F.; et al. Inhibition of 5-lipoxygenase by MK886 augments the antitumor activity of celecoxib in human colon cancer cells. Mol. Cancer Ther. 2006, 5, 2716-2726.
-
(2006)
Mol. Cancer Ther.
, vol.5
, pp. 2716-2726
-
-
Cianchi, F.1
Cortesini, C.2
Magnelli, L.3
Fanti, E.4
Papucci, L.5
Schiavone, N.6
Messerini, L.7
Vannacci, A.8
Capaccioli, S.9
Perna, F.10
-
3
-
-
23844530173
-
Leukotriene modifiers as potential therapeutics for cardiovascular disease
-
Funk, C.D. Leukotriene modifiers as potential therapeutics for cardiovascular disease. Nat. Rev. Drug Discov. 2005, 4, 664-672.
-
(2005)
Nat. Rev. Drug Discov.
, vol.4
, pp. 664-672
-
-
Funk, C.D.1
-
4
-
-
33744831188
-
Design, molecular modeling, synthesis, and anti-hiv-1 activity of new indolyl aryl sulfones. novel derivatives of the indole-2-carboxamide
-
Ragno, R.; Coluccia, A.; La Regina, G.; De Martino, G.; Piscitelli, F.; Lavecchia, A.; Novellino, E.; Bergamini, A.; Ciaprini, C.; Sinistro, A.; et al. Design, Molecular modeling, Synthesis, And anti-HIV-1 activity of new indolyl aryl sulfones. Novel derivatives of the indole-2-carboxamide. J. Med. Chem. 2006, 49, 3172-3184.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 3172-3184
-
-
Ragno, R.1
Coluccia, A.2
La Regina, G.3
De Martino, G.4
Piscitelli, F.5
Lavecchia, A.6
Novellino, E.7
Bergamini, A.8
Ciaprini, C.9
Sinistro, A.10
-
5
-
-
33644752667
-
Development of a novel, highly efficient halide-catalyzed sulfenylation of indoles
-
Tudge, M.; Tamiya, M.; Savarin, C.; Humphrey, G.R. Development of a novel, highly efficient halide-catalyzed sulfenylation of indoles. Org. Lett. 2006, 8, 565-568.
-
(2006)
Org. Lett.
, vol.8
, pp. 565-568
-
-
Tudge, M.1
Tamiya, M.2
Savarin, C.3
Humphrey, G.R.4
-
6
-
-
34247599799
-
The first entry to 5,6- dihydroxy-3-mercaptoindole, 5-hydroxy-3- mercaptoindole and their 2-carbomethoxy derivatives by a mild thiocyanation/reduction methodology
-
Pezzella, A.; Palma, A.; Iadonisi, A.; Napolitano, A.; d'Ischia, M. The first entry to 5,6- dihydroxy-3-mercaptoindole, 5-hydroxy-3-mercaptoindole and their 2-carbomethoxy derivatives by a mild thiocyanation/reduction methodology. Tetrahedron Lett. 2007, 48, 3883-3886.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 3883-3886
-
-
Pezzella, A.1
Palma, A.2
Iadonisi, A.3
Napolitano, A.4
D'Ischia, M.5
-
7
-
-
17744364542
-
Ferric(iii) chloridepromoted electrophilic thiocyanation of aromatic and heteroaromatic compounds
-
Yadav, J.S.; Reddy, B.V. S.; Krishna, A.D.; Reddy, C.S.; Narsaiah, A.V. Ferric(III) chloridepromoted electrophilic thiocyanation of aromatic and heteroaromatic compounds. Synthesis 2005, 961-964.
-
(2005)
Synthesis
, pp. 961-964
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Krishna, A.D.3
Reddy, C.S.4
Narsaiah, A.V.5
-
8
-
-
23044459885
-
Regioselective thiocyanation of aromatic and heteroaromatic compounds using ammonium thiocyanate and oxone
-
Wu, G.; Liu, Q.; Shen, Y.; Wu, W.; Wu, L. Regioselective thiocyanation of aromatic and heteroaromatic compounds using ammonium thiocyanate and oxone. Tetrahedron Lett. 2005, 46, 5831-5834.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 5831-5834
-
-
Wu, G.1
Liu, Q.2
Shen, Y.3
Wu, W.4
Wu, L.5
-
10
-
-
84855709870
-
-
Derek, W.J., Risto, L., Eds.; Springer-Verlag: Berlin Heidelberg, Germany
-
Alberto, E.E.; Braga, A.L. Selenium and Tellurium Chemistry - From Small Molecules to Biomolecules and Materials; Derek, W.J., Risto, L., Eds.; Springer-Verlag: Berlin Heidelberg, Germany, 2011.
-
(2011)
Selenium and Tellurium Chemistry - From Small Molecules to Biomolecules and Materials;
-
-
Alberto, E.E.1
Braga, A.L.2
-
13
-
-
65349152731
-
Synthesis of vinyl selenides
-
Perin, G.; Lenardão, E.J.; Jacob, R.G.; Panatieri, R.B. Synthesis of vinyl selenides. Chem. Rev. 2009, 109, 1277-1301.
-
(2009)
Chem. Rev.
, vol.109
, pp. 1277-1301
-
-
Perin, G.1
Lenardão, E.J.2
Jacob, R.G.3
Panatieri, R.B.4
-
14
-
-
70350339652
-
Green chemistry with selenium reagents: Development of efficient catalytic reactions
-
Freudendahl, D.M.; Santoro, S.; Shahzad, S.A.; Santi, C.; Wirth, T. Green chemistry with selenium reagents: Development of efficient catalytic reactions. Angew. Chem. Int. Ed. Engl. 2009, 48, 8409-8411.
-
(2009)
Angew. Chem. Int. Ed. Engl.
, vol.48
, pp. 8409-8411
-
-
Freudendahl, D.M.1
Santoro, S.2
Shahzad, S.A.3
Santi, C.4
Wirth, T.5
-
15
-
-
78649931871
-
Organoselenium compounds as catalysts in nature and laboratory
-
Santi, C.; Santoro, S.; Battistelli, B. Organoselenium compounds as catalysts in nature and laboratory. Curr. Org. Chem. 2010, 14, 2442-2462.
-
(2010)
Curr. Org. Chem.
, vol.14
, pp. 2442-2462
-
-
Santi, C.1
Santoro, S.2
Battistelli, B.3
-
16
-
-
69549110385
-
Synthesis of 3-sulfenyl- and 3-selenylindoles by the pd/cu-catalyzed coupling of n,n-dialkyl-2-iodoanilines and terminal alkynes, followed by n-bu4ni-induced electrophilic cyclization
-
Chen, Y.; Cho, C.-H; Shi, F.; Larock, R.C. Synthesis of 3-sulfenyl- and 3-selenylindoles by the Pd/Cu-catalyzed coupling of N,N-dialkyl-2-iodoanilines and terminal alkynes, followed by n-Bu4NI-induced electrophilic cyclization. J. Org. Chem. 2009, 74, 6802-6811.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 6802-6811
-
-
Chen, Y.1
Cho, C.-H.2
Shi, F.3
Larock, R.C.4
-
17
-
-
59649088558
-
A novel synthetic route to 3-sulfenyland 3- selenylindoles by n-bu4ni-induced electrophilic cyclization
-
Chen, Y.; Cho, C.-H.; Shi, F.; Larock, R.C. A novel synthetic route to 3-sulfenyland 3- selenylindoles by n-Bu4NI-induced electrophilic cyclization. Org. Lett. 2009, 11, 173-176.
-
(2009)
Org. Lett.
, vol.11
, pp. 173-176
-
-
Chen, Y.1
Cho, C.-H.2
Shi, F.3
Larock, R.C.4
-
18
-
-
80054736113
-
Iron-facilitated iodinemediated electrophilic annulation of n,n-dimethyl-2-alkynylanilines with disulfides or diselenides
-
Du, H.-A; Tang, R.-Y; Deng, C.-L; Liu, Y.; Li, J.-H; Zhang, X.-G. Iron-facilitated iodinemediated electrophilic annulation of N,N-dimethyl-2- alkynylanilines with disulfides or diselenides. Adv. Synth. Catal. 2011, 353, 2739-2748.
-
(2011)
Adv. Synth. Catal.
, vol.353
, pp. 2739-2748
-
-
Du, H.-A.1
Tang, R.-Y.2
Deng, C.-L.3
Liu, Y.4
Li, J.-H.5
Zhang, X.-G.6
-
19
-
-
84866375891
-
An efficient synthesis of 2-bromo(chloro)-3- selenyl(sulfenyl)indoles via tandem reactions of 2-(gem-dibromo(chloro)vinyl)anilines with diselenides(disulfides)
-
Liu, J.; Li, P.; Chen, W.; Wang, L. An efficient synthesis of 2-bromo(chloro)-3- selenyl(sulfenyl)indoles via tandem reactions of 2-(gem-dibromo(chloro)vinyl)anilines with diselenides(disulfides). Chem. Commun. 2012, 48, 10052-10054.
-
(2012)
Chem. Commun.
, vol.48
, pp. 10052-10054
-
-
Liu, J.1
Li, P.2
Chen, W.3
Wang, L.4
-
20
-
-
84986511297
-
Synthesis of indoles via amidoselenation
-
Izumi, T.; Sugano, M.; Konno, T. Synthesis of indoles via amidoselenation. J. Heterocycl. Chem. 1992, 29, 899-904.
-
(1992)
J. Heterocycl. Chem.
, vol.29
, pp. 899-904
-
-
Izumi, T.1
Sugano, M.2
Konno, T.3
-
21
-
-
0001763188
-
La transformation d'indolines en indoles et d'autres reactions apparentees
-
Barton, D.H. R.; Lusinchi, X; Milliet, P. La transformation d'indolines en indoles et d'autres reactions apparentees. Tetrahedron Lett. 1982, 23, 4949-4952.
-
(1982)
Tetrahedron Lett.
, vol.23
, pp. 4949-4952
-
-
Barton, D.H.R.1
Lusinchi, X.2
Milliet, P.3
-
22
-
-
0000956311
-
Studies on the reaction of primary and secondary amines with phenylseleninic anhydride and with phenylseleninic acid
-
Barton, D.H. R.; Lusinchi, X.; Milliet, P. Studies on the reaction of primary and secondary amines with phenylseleninic anhydride and with phenylseleninic acid. Tetrahedron 1985, 41, 4727-4738.
-
(1985)
Tetrahedron
, vol.41
, pp. 4727-4738
-
-
Barton, D.H.R.1
Lusinchi, X.2
Milliet, P.3
-
23
-
-
0028070265
-
Aspidosperma alkaloids via cyclization of secodine intermediate: Synthesis of (+/-)-3-oxovincadifformine ethyl ester
-
Danieli, B.; Lesma, G.; Palmisano, G.; Passarella, D.; Silvani, A. Aspidosperma alkaloids via cyclization of secodine intermediate: synthesis of (+/-)-3-oxovincadifformine ethyl ester. Tetrahedron 1994, 50, 6941-6954.
-
(1994)
Tetrahedron
, vol.50
, pp. 6941-6954
-
-
Danieli, B.1
Lesma, G.2
Palmisano, G.3
Passarella, D.4
Silvani, A.5
-
24
-
-
5344256415
-
An improved procedure for the conversion of indolines into indoles
-
Ninomiya, I; Kiguchi, T.; Hashimoto, C. An improved procedure for the conversion of indolines into indoles. Tetrahedron Lett. 1985, 26, 4183-4186.
-
(1985)
Tetrahedron Lett.
, vol.26
, pp. 4183-4186
-
-
Ninomiya, I.1
Kiguchi, T.2
Hashimoto, C.3
-
25
-
-
49049128635
-
Reaction of 2-acylphenylselenocyanates with hydroxylamine and phenylhydrazine
-
Ames, D.E.; Singh, A.G.; Smyth, W.F. Reaction of 2- acylphenylselenocyanates with hydroxylamine and phenylhydrazine. Tetrahedron 1983, 39, 831-833.
-
(1983)
Tetrahedron
, vol.39
, pp. 831-833
-
-
Ames, D.E.1
Singh, A.G.2
Smyth, W.F.3
-
26
-
-
77956943946
-
Iron-catalyzed sulfenylation of indoles with disulfides promoted by a catalytic amount of iodine
-
Fang, X.L.; Tang, R.Y.; Zhong, P.; Li, J.H. Iron-catalyzed sulfenylation of indoles with disulfides promoted by a catalytic amount of iodine. Synthesis 2009, 4183-4189.
-
(2009)
Synthesis
, pp. 4183-4189
-
-
Fang, X.L.1
Tang, R.Y.2
Zhong, P.3
Li, J.H.4
-
27
-
-
37249093419
-
Novel brønsted acid catalyzed three-component alkylations of indoles with n-phenylselenophthalimide and styrenes
-
Zhao, X.; Yu, Z.; Xu, T.; Wu, P.; Yu, H. Novel Brønsted acid catalyzed three-component alkylations of indoles with N-phenylselenophthalimide and styrenes. Org. Lett. 2007, 9, 5263-5266.
-
(2007)
Org. Lett.
, vol.9
, pp. 5263-5266
-
-
Zhao, X.1
Yu, Z.2
Xu, T.3
Wu, P.4
Yu, H.5
-
28
-
-
84868494249
-
Efficient synthesis of 3-selanyl- and 3-sulfanylindoles employing trichloroisocyanuric acid and dichalcogenides
-
Silveira, C.C.; Mendes, S.R.; Wolf, L.; Martins, G.M.; von Mühlen, L. Efficient synthesis of 3-selanyl- and 3-sulfanylindoles employing trichloroisocyanuric acid and dichalcogenides. Tetrahedron 2012, 68, 10464-10469.
-
(2012)
Tetrahedron
, vol.68
, pp. 10464-10469
-
-
Silveira, C.C.1
Mendes, S.R.2
Wolf, L.3
Martins, G.M.4
Von Mühlen, L.5
-
29
-
-
80053295209
-
Advances on biomass pretreatment using ionic liquids: An overview
-
Tadesse, H.; Luque, R. Advances on biomass pretreatment using ionic liquids: An overview. Energy Environ. Sci. 2011, 4, 3913-3929.
-
(2011)
Energy Environ. Sci.
, vol.4
, pp. 3913-3929
-
-
Tadesse, H.1
Luque, R.2
-
30
-
-
0347417134
-
Room-temperature ionic liquids. solvents for synthesis and catalysis
-
Welton, T. Room-temperature ionic liquids. Solvents for synthesis and catalysis. Chem. Rev. 1999, 99, 2071-2083.
-
(1999)
Chem. Rev.
, vol.99
, pp. 2071-2083
-
-
Welton, T.1
-
31
-
-
0036809725
-
Ionic liquid (molten salt) phase organometallic catalysis
-
Dupont, J.; Souza, R.F.; Suarez, P.A.Z. Ionic liquid (molten salt) phase organometallic catalysis. Chem. Rev. 2002, 102, 3667-3692.
-
(2002)
Chem. Rev.
, vol.102
, pp. 3667-3692
-
-
Dupont, J.1
Souza, R.F.2
Suarez, P.A.Z.3
-
33
-
-
47349086495
-
Ionic liquids in heterocyclic synthesis
-
Martins, M.A. P.; Frizzo, C.P.; Moreira, D.N.; Zanatta, N.; Bonacorso, H.G. Ionic Liquids in Heterocyclic Synthesis. Chem. Rev. 2008, 108, 2015-2050.
-
(2008)
Chem. Rev.
, vol.108
, pp. 2015-2050
-
-
Martins, M.A.P.1
Frizzo, C.P.2
Moreira, D.N.3
Zanatta, N.4
Bonacorso, H.G.5
-
34
-
-
33748426457
-
Selenium and tellurium-based ionic liquids and their use in the synthesis of octahydroacridines
-
Lenardão, E.J.; Mendes, S.R.; Ferreira, P.C.; Perin, G.; Silveira, C.C.; Jacob, R.G. Selenium- and tellurium-based ionic liquids and their use in the synthesis of octahydroacridines. Tetrahedron Lett. 2006, 47, 7439-7442.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 7439-7442
-
-
Lenardão, E.J.1
Mendes, S.R.2
Ferreira, P.C.3
Perin, G.4
Silveira, C.C.5
Jacob, R.G.6
-
35
-
-
67650931358
-
Selenonium ionic liquid as efficient catalyst for the baylis-hillman reaction
-
Lenardão, E.J.; Feijó, J.O.; Thurow, S.; Perin, G.; Jacob, R.G.; Silveira, C.C. Selenonium ionic liquid as efficient catalyst for the Baylis-Hillman reaction. Tetrahedron Lett. 2009, 50, 5215-5217.
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 5215-5217
-
-
Lenardão, E.J.1
Feijó, J.O.2
Thurow, S.3
Perin, G.4
Jacob, R.G.5
Silveira, C.C.6
-
36
-
-
39249084454
-
Selenonium ionic liquid as an efficient catalyst for the synthesis of thioacetals under solvent-free conditions
-
Lenardão, E.J.; Borges, E.L.; Mendes, S.R.; Perin, G.; Jacob, R.G. Selenonium ionic liquid as an efficient catalyst for the synthesis of thioacetals under solvent-free conditions. Tetrahedron Lett. 2008, 49, 1919-1921.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 1919-1921
-
-
Lenardão, E.J.1
Borges, E.L.2
Mendes, S.R.3
Perin, G.4
Jacob, R.G.5
-
37
-
-
0037112582
-
Ionic liquids containing anionic selenium species: Applications for the oxidative carbonylation of aniline
-
For the synthesis of [bmim][SeO2(OCH3)] see: Kim, H.S.; Kim, Y.J.; Lee, H.; Park, K.Y.; Lee, C.; Chin, C.S. Ionic Liquids Containing Anionic Selenium Species: Applications for the Oxidative Carbonylation of Aniline. Angew. Chem. Int. Ed. Engl. 2002, 41, 4300-4303.
-
(2002)
Angew. Chem. Int. Ed. Engl.
, vol.41
, pp. 4300-4303
-
-
Kim, H.S.1
Kim, Y.J.2
Lee, H.3
Park, K.Y.4
Lee, C.5
Chin, C.S.6
-
38
-
-
78651110462
-
Base-free oxidation of thiols to disulfides using selenium ionic liquid
-
Thurow, S.; Pereira, V.A.; Martinez, D.M.; Alves, D.; Perin, G.; Jacob, R.G.; Lenardão, E.J. Base-free oxidation of thiols to disulfides using selenium ionic liquid. Tetrahedron Lett. 2011, 52, 640-643.
-
(2011)
Tetrahedron Lett.
, vol.52
, pp. 640-643
-
-
Thurow, S.1
Pereira, V.A.2
Martinez, D.M.3
Alves, D.4
Perin, G.5
Jacob, R.G.6
Lenardão, E.J.7
-
39
-
-
84859782750
-
Synthesis of vinyl sulfides under base-free conditions using selenium ionic liquid
-
Thurow, S.; Ostosi, N.T.; Mendes, S.R.; Jacob, R.G.; Lenardão, E.J. Synthesis of vinyl sulfides under base-free conditions using selenium ionic liquid. Tetrahedron Lett. 2012, 53, 2651-2653.
-
(2012)
Tetrahedron Lett.
, vol.53
, pp. 2651-2653
-
-
Thurow, S.1
Ostosi, N.T.2
Mendes, S.R.3
Jacob, R.G.4
Lenardão, E.J.5
-
40
-
-
0001591616
-
N-phenylselenophthalimide (npsp) a valuable selenenylating agent
-
Nicolaou, K.C.; Petatis, N.A.; Claremon, D.A. N-Phenylselenophthalimide (NPSP) a valuable selenenylating agent. Tetrahedron 1985, 41, 4835-4841.
-
(1985)
Tetrahedron
, vol.41
, pp. 4835-4841
-
-
Nicolaou, K.C.1
Petatis, N.A.2
Claremon, D.A.3
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