-
1
-
-
0000699428
-
Structure elucidation of streptindole, a novel genotoxic metabolite isolated from intestinal bacteria
-
Osawa, T.; Namiki, M. Structure elucidation of streptindole, a novel genotoxic metabolite isolated from intestinal bacteria. Tetrahedron Lett. 1983, 24, 4719.
-
(1983)
Tetrahedron Lett
, vol.24
, pp. 4719
-
-
Osawa, T.1
Namiki, M.2
-
2
-
-
2942559219
-
Zeolite-catalyzed electrophilic substitution reaction of indoles with aldehydes: Synthesis of bis(indolyl)methanes
-
Karthik, M.; Tripathi, A. K.; Gupta, N. M.; Palanichamy, M.; Murugeson, V. Zeolite-catalyzed electrophilic substitution reaction of indoles with aldehydes: Synthesis of bis(indolyl)methanes. Catal. Commun. 2004, 5, 371.
-
(2004)
Catal. Commun
, vol.5
, pp. 371
-
-
Karthik, M.1
Tripathi, A.K.2
Gupta, N.M.3
Palanichamy, M.4
Murugeson, V.5
-
3
-
-
5344239616
-
Lewis acid-catalyzed electrophilic substitution of indole with aldehydes and Schiff's bases under microwave solvent-free irradiation
-
Xia, M.; Wang, S.; Yuan, W. Lewis acid-catalyzed electrophilic substitution of indole with aldehydes and Schiff's bases under microwave solvent-free irradiation. Synth. Commun. 2004, 34, 3175.
-
(2004)
Synth. Commun
, vol.34
, pp. 3175
-
-
Xia, M.1
Wang, S.2
Yuan, W.3
-
4
-
-
0028265837
-
Direct synthesis of aryldipyrromethanes
-
Vigmond, S. J.; Chang, M. C.; Kallury, K. M. R.; Thompson, M. Direct synthesis of aryldipyrromethanes. Tetrahedron Lett. 1994, 35, 2455.
-
(1994)
Tetrahedron Lett
, vol.35
, pp. 2455
-
-
Vigmond, S.J.1
Chang, M.C.2
Kallury, K.M.R.3
Thompson, M.4
-
5
-
-
3943087054
-
Syntheses of some substituted di-indolylmethanes in aqueous medium at room temperature
-
Kamal, A.; Qureshi, A. A. Syntheses of some substituted di-indolylmethanes in aqueous medium at room temperature. Tetrahedron 1963, 19, 513.
-
(1963)
Tetrahedron
, vol.19
, pp. 513
-
-
Kamal, A.1
Qureshi, A.A.2
-
6
-
-
1042298780
-
Facile synthesis of bis(indolyl)-methanes using catalytic amount of iodine at room temperature under solvent-free conditions
-
Ji, S. J.; Wang, S. Y.; Zhang, Y.; Loh, T.-P. Facile synthesis of bis(indolyl)-methanes using catalytic amount of iodine at room temperature under solvent-free conditions. Tetrahedron 2004, 60, 2051.
-
(2004)
Tetrahedron
, vol.60
, pp. 2051
-
-
Ji, S.J.1
Wang, S.Y.2
Zhang, Y.3
Loh, T.-P.4
-
7
-
-
0034040349
-
A convenient method of synthesis of bis-indolylmethanes: Indium trichloride-catalyzed reactions of indole with aldehydes and Schiff's bases
-
Babu, G.; Sridhar, N.; Perumal, P. T. A convenient method of synthesis of bis-indolylmethanes: Indium trichloride-catalyzed reactions of indole with aldehydes and Schiff's bases. Synth. Commun. 2000, 30, 1609.
-
(2000)
Synth. Commun
, vol.30
, pp. 1609
-
-
Babu, G.1
Sridhar, N.2
Perumal, P.T.3
-
8
-
-
0027989477
-
One-flask synthesis of meso-substituted dipyrromethanes and their application in the synthesis of trans-substituted porphyrin building blocks
-
Lee, C. H.; Lindsey, J. S. One-flask synthesis of meso-substituted dipyrromethanes and their application in the synthesis of trans-substituted porphyrin building blocks. Tetrahedron 1994, 50, 11427.
-
(1994)
Tetrahedron
, vol.50
, pp. 11427
-
-
Lee, C.H.1
Lindsey, J.S.2
-
9
-
-
0036166575
-
Electrophilic substitution of indoles catalyzed by triphenyl phosphonium perchlorate: Synthesis of 3-acetyl indoles and bisindolylmethane derivatives
-
Nagarajan, R.; Perumal, P. T. Electrophilic substitution of indoles catalyzed by triphenyl phosphonium perchlorate: Synthesis of 3-acetyl indoles and bisindolylmethane derivatives. Synth. Commun. 2002, 32, 105.
-
(2002)
Synth. Commun
, vol.32
, pp. 105
-
-
Nagarajan, R.1
Perumal, P.T.2
-
11
-
-
9744285166
-
An efficient procedure for the preparation of mono- and di- bis-indolyl methanes catalyzed by molibdatophosphoric acid
-
Zolfigol, M. A.; Salehi, P.; Shiri, M. An efficient procedure for the preparation of mono- and di- bis-indolyl methanes catalyzed by molibdatophosphoric acid. Phosphorus Sulfur Silicon Relat. Elem. 2004, 179, 2273.
-
(2004)
Phosphorus Sulfur Silicon Relat. Elem
, vol.179
, pp. 2273
-
-
Zolfigol, M.A.1
Salehi, P.2
Shiri, M.3
-
12
-
-
4544309609
-
A versatile and practical synthesis of bis(indolyl)methanes/bis(indolyl) glycoconjugates catalyzed by trichloro-1,3,5-triazine
-
Sharma, G. V. M.; Reddy, J. J.; Lakshmi, P. S.; Krishna, P. R. A versatile and practical synthesis of bis(indolyl)methanes/bis(indolyl) glycoconjugates catalyzed by trichloro-1,3,5-triazine. Tetrahedron Lett. 2004, 45, 7729.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 7729
-
-
Sharma, G.V.M.1
Reddy, J.J.2
Lakshmi, P.S.3
Krishna, P.R.4
-
13
-
-
0347929603
-
Structure of the second polymorph of niobium pentachloride
-
Cotton, F. A.; Kibala, P. A.; Matusz, M.; Sandor, R. B. W. Structure of the second polymorph of niobium pentachloride. Acta Cryst. 1991, 47, 2435.
-
(1991)
Acta Cryst
, vol.47
, pp. 2435
-
-
Cotton, F.A.1
Kibala, P.A.2
Matusz, M.3
Sandor, R.B.W.4
-
14
-
-
12744251087
-
Niobium pentachloride in organic synthesis: Applications and perspectives
-
Kleber, C.; Andrade, Z. Niobium pentachloride in organic synthesis: Applications and perspectives. Curr. Org. Synth. 2004, 1, 333.
-
(2004)
Curr. Org. Synth
, vol.1
, pp. 333
-
-
Kleber, C.1
Andrade, Z.2
-
15
-
-
33750702149
-
Recent applications of niobium catalysts in organic synthesis
-
Kleber, C.; Andrade, Z.; Rocha, R. O. Recent applications of niobium catalysts in organic synthesis. Mini-Rev. Org. Chem. 2006, 3, 271.
-
(2006)
Mini-Rev. Org. Chem
, vol.3
, pp. 271
-
-
Kleber, C.1
Andrade, Z.2
Rocha, R.O.3
-
16
-
-
0037575807
-
Lewis acid catalysis of the Diels-Alder reaction using niobium and tantalum chlorides in the presence of coordinating ligands
-
Howarth, J.; Gillespie, K. Lewis acid catalysis of the Diels-Alder reaction using niobium and tantalum chlorides in the presence of coordinating ligands. Molecules 2000, 5, 993.
-
(2000)
Molecules
, vol.5
, pp. 993
-
-
Howarth, J.1
Gillespie, K.2
-
17
-
-
0011165604
-
Niobium pentachloride-catalysed ring opening of epoxides
-
Constantino, M. G.; Lacerda, Jr., V.; Aragao, V. Niobium pentachloride-catalysed ring opening of epoxides. Molecules 2001, 6, 770.
-
(2001)
Molecules
, vol.6
, pp. 770
-
-
Constantino, M.G.1
Lacerda Jr., V.2
Aragao, V.3
-
18
-
-
0035840404
-
Niobium(V) chloride-mediated allylation of aldehydes: Scope and stereoselectivity
-
Andrade, C. K. Z.; Azevedo, N. R. Niobium(V) chloride-mediated allylation of aldehydes: Scope and stereoselectivity. Tetrahedron Lett. 2001, 42, 6473.
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 6473
-
-
Andrade, C.K.Z.1
Azevedo, N.R.2
-
19
-
-
33847056248
-
5-catalyzed one-pot Mannich-type reaction: Three-component synthesis of b-amino carbonyl compounds
-
5-catalyzed one-pot Mannich-type reaction: Three-component synthesis of b-amino carbonyl compounds. Tetrahedron Lett. 2007, 48, 2071.
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 2071
-
-
Wang, R.1
Li, B.G.2
Huang, T.K.3
Shi, L.4
Lu, X.X.5
-
20
-
-
35348993725
-
Niobium(V) pentachloride: An efficient catalyst for C, N, O, and S-nucleophilic substitution reactions of benzylic alcohols
-
Yadav, J. S.; Bhunia, D. C.; Krishna, K. V.; Srihari, P. Niobium(V) pentachloride: An efficient catalyst for C, N, O, and S-nucleophilic substitution reactions of benzylic alcohols. Tetrahedron Lett. 2007, 48, 8306.
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 8306
-
-
Yadav, J.S.1
Bhunia, D.C.2
Krishna, K.V.3
Srihari, P.4
-
21
-
-
36348970206
-
A convenient synthesis of bis(indolyl)methanes catalyzed by diphosphooctadecatungstic acid
-
Heravi, M. M.; Bakhtiari, K.; Fatehi, A.; Bamoharram, F. F. A convenient synthesis of bis(indolyl)methanes catalyzed by diphosphooctadecatungstic acid. Catal. Commun. 2008, 9, 289.
-
(2008)
Catal. Commun
, vol.9
, pp. 289
-
-
Heravi, M.M.1
Bakhtiari, K.2
Fatehi, A.3
Bamoharram, F.F.4
-
22
-
-
34447279557
-
Preparation of indolylmethanes catalyzed by metal hydrogen sulfates
-
Niknam, K.; Zolfigol, M. A.; Sadabadi, T.; Nejati, A. Preparation of indolylmethanes catalyzed by metal hydrogen sulfates. J. Iranian Chem. Soc. 2006, 3, 318.
-
(2006)
J. Iranian Chem. Soc
, vol.3
, pp. 318
-
-
Niknam, K.1
Zolfigol, M.A.2
Sadabadi, T.3
Nejati, A.4
-
23
-
-
26444589070
-
An efficient and practical synthesis of bis(indolyl)methanes catalyzed by aminosulfonic acid under ultrasound
-
Li, J. T.; Dai, H. G.; Xu, W. Z.; Li, T. S. An efficient and practical synthesis of bis(indolyl)methanes catalyzed by aminosulfonic acid under ultrasound. Ultrasonics Sonochem. 2006, 13, 24.
-
(2006)
Ultrasonics Sonochem
, vol.13
, pp. 24
-
-
Li, J.T.1
Dai, H.G.2
Xu, W.Z.3
Li, T.S.4
-
24
-
-
39449108320
-
12-Tungstophosphoric acid supported on zirconia as an efficient and heterogeneous catalyst for the synthesis of bis(indolyl)methanes and tris(indolyl)methanes
-
Satam, J. R.; Parghi, K. D.; Jayaram, R. V. 12-Tungstophosphoric acid supported on zirconia as an efficient and heterogeneous catalyst for the synthesis of bis(indolyl)methanes and tris(indolyl)methanes. Catal. Commun. 2008, 9, 1071.
-
(2008)
Catal. Commun
, vol.9
, pp. 1071
-
-
Satam, J.R.1
Parghi, K.D.2
Jayaram, R.V.3
-
25
-
-
31444448205
-
An efficient and clean synthesis of bis(indolyl)-methanes in a protic solvent at room temperature
-
Deb, M. L.; Bhuyan, P. J. An efficient and clean synthesis of bis(indolyl)-methanes in a protic solvent at room temperature. Tetrahedron Lett. 2006, 47, 1441.
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 1441
-
-
Deb, M.L.1
Bhuyan, P.J.2
-
26
-
-
34248348657
-
Ammonium chloride-catalyzed one-pot synthesis of diindolylmethanes under solvent-free conditions
-
Azizian, J.; Teimouri, F.; Mohammadizadeh, M. R. Ammonium chloride-catalyzed one-pot synthesis of diindolylmethanes under solvent-free conditions. Catal. Commun. 2007, 8, 1117.
-
(2007)
Catal. Commun
, vol.8
, pp. 1117
-
-
Azizian, J.1
Teimouri, F.2
Mohammadizadeh, M.R.3
-
27
-
-
33646864765
-
-
2O/silica gel as a new, efficient, and a highly water-tolerant catalyst system for facile condensation of indoles with carbonyl compounds under solvent-free conditions. J. Mol. Catal. A: Chem. 2006, 253, 249.
-
2O/silica gel as a new, efficient, and a highly water-tolerant catalyst system for facile condensation of indoles with carbonyl compounds under solvent-free conditions. J. Mol. Catal. A: Chem. 2006, 253, 249.
-
-
-
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