-
1
-
-
0029085525
-
Further brominated bis- and tris-indole alkaloids from the deep-water new caledonian marine sponge Orina sp
-
(a) Riccio, R.; Bifulco, G.; Bruno, I. Further brominated bis- and tris-indole alkaloids from the deep-water new caledonian marine sponge Orina sp. J. Nat. Prod. 1995, 58, 1254;
-
(1995)
J. Nat. Prod.
, vol.58
, pp. 1254
-
-
Riccio, R.1
Bifulco, G.2
Bruno, I.3
-
2
-
-
0028605225
-
Vibrindole A, a metabolite of the marine bacterium Vibrio parahaemolyticus, isolated from toxic mucus of the boxfish Ostracion cubicus
-
(b) Bell, R.; Carmelli, S.; Sar, N. Vibrindole A, a metabolite of the marine bacterium Vibrio parahaemolyticus, isolated from toxic mucus of the boxfish Ostracion cubicus. J. Nat. Prod. 1994, 57, 1587;
-
(1994)
J. Nat. Prod.
, vol.57
, pp. 1587
-
-
Bell, R.1
Carmelli, S.2
Sar, N.3
-
3
-
-
0025998158
-
6-Bromotryptamine derivatives from the Gulf of California tunicate Didemnum candidum
-
(c) Fahy, E.; Potts, B. C. M.; Faulkner, D. J.; Smith, K. 6-Bromotryptamine derivatives from the Gulf of California tunicate Didemnum candidum. J. Nat. Prod. 1991, 54, 564.
-
(1991)
J. Nat. Prod.
, vol.54
, pp. 564
-
-
Fahy, E.1
Potts, B.C.M.2
Faulkner, D.J.3
Smith, K.4
-
4
-
-
0037087501
-
Diindolylmethane (DIM) is produced when the substance indole 3-carbinol (I3C) is digested
-
Hong, C.; Firestone, G. L.; Bjelanes, L. F. Diindolylmethane (DIM) is produced when the substance indole 3-carbinol (I3C) is digested. Biochem. Pharmacol. 2002, 63, 1085.
-
(2002)
Biochem. Pharmacol.
, vol.63
, pp. 1085
-
-
Hong, C.1
Firestone, G.L.2
Bjelanes, L.F.3
-
5
-
-
31544460087
-
Oxidized bis(indolyl)- methane: A simple and efficient chromogenic-sensing molecule based on the proton transfer signaling mode
-
Xiaoming, H.; Shuzhen, H.; Liu, K.; Guo, Y.; Jian, X.; Shao, S. Oxidized bis(indolyl)- methane: A simple and efficient chromogenic-sensing molecule based on the proton transfer signaling mode. Org. Lett. 2006, 8, 333.
-
(2006)
Org. Lett.
, vol.8
, pp. 333
-
-
Xiaoming, H.1
Shuzhen, H.2
Liu, K.3
Guo, Y.4
Jian, X.5
Shao, S.6
-
6
-
-
31544464135
-
Inhibition of bladder tumor growth by 1,1-bis(30-indolyl)-1-(p- substitutedphenyl)methanes: A new class of peroxisome proliferator-activated receptor agonists
-
Wassim, K.; Sudhakar, C.; Maen, A.; Gina, N.; Stephen, S.; Ashish, M. K. Inhibition of bladder tumor growth by 1,1-bis(30-indolyl)-1-(p- substitutedphenyl)methanes: A new class of peroxisome proliferator-activated receptor agonists. Cancer Res. 2006, 66, 412.
-
(2006)
Cancer Res.
, vol.66
, pp. 412
-
-
Wassim, K.1
Sudhakar, C.2
Maen, A.3
Gina, N.4
Stephen, S.5
Ashish, M.K.6
-
7
-
-
0035042642
-
Lithium perchlorate-catalyzed reaction of indoles: An expeditious synthesis of bis(indolyl)- methanes
-
Yadav, J. S.; Reddy, B. V. S.; Murthy, C. V. S. R.; Kumar, G. M.; Madan, C. Lithium perchlorate-catalyzed reaction of indoles: An expeditious synthesis of bis(indolyl)- methanes. Synthesis 2001, 5, 783.
-
(2001)
Synthesis
, vol.5
, pp. 783
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Murthy, C.V.S.R.3
Kumar, G.M.4
Madan, C.5
-
8
-
-
0037016927
-
InCl3- and In(otf)x-catalyzed reaction of 3-acetylindolylmethanes and indolylquinoline derivatives
-
Nagarajan, R.; Perumal, P. T. InCl3- and In(otf)x-catalyzed reaction of 3-acetylindolylmethanes and indolylquinoline derivatives. Tetrahedron 2002, 58, 1229.
-
(2002)
Tetrahedron
, vol.58
, pp. 1229
-
-
Nagarajan, R.1
Perumal, P.T.2
-
9
-
-
2342483570
-
InCl3-catalysed conjugate addition of indoles with electron-deficient olefins
-
Mi, X. L.; Luo, S. Z.; He, J. Q.; Cheng, J. P. InCl3-catalysed conjugate addition of indoles with electron-deficient olefins. Tetrahedron Lett. 2004, 45, 4567.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 4567
-
-
Mi, X.L.1
Luo, S.Z.2
He, J.Q.3
Cheng, J.P.4
-
10
-
-
19944361904
-
Sc(OTf) 3-catalyzed efficient synthesis of b,b-bis(indolyl) ketones by the double indolylation of acetic acid 2-methylene-3-oxobutyl ester
-
Ma, S.; Yu, S.; Peng, Z. Sc(OTf)3-catalyzed efficient synthesis of b,b-bis(indolyl) ketones by the double indolylation of acetic acid 2-methylene-3-oxobutyl ester. Org. Biomol. Chem. 2005, 3, 1933.
-
(2005)
Org. Biomol. Chem.
, vol.3
, pp. 1933
-
-
Ma, S.1
Yu, S.2
Peng, Z.3
-
11
-
-
0037463441
-
Molecular iodine-catalyzed efficient and highly rapid synthesis of bis-indolyl-methane under mild conditions
-
Bandagar, B. P.; Shaikh, K. A. Molecular iodine-catalyzed efficient and highly rapid synthesis of bis-indolyl-methane under mild conditions. Tetrahedron Lett. 2003, 44, 1959.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 1959
-
-
Bandagar, B.P.1
Shaikh, K.A.2
-
12
-
-
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
-
13
-
-
33745933302
-
Zirconyl(IV) chloride-catalysed reaction of indoles: An expeditious synthesis of bis(indolyl) methanes
-
Nagawade, R. R.; Shinde, D. B. Zirconyl(IV) chloride-catalysed reaction of indoles: An expeditious synthesis of bis(indolyl) methanes. Acta Chim. Slov. 2006, 53, 210.
-
(2006)
Acta Chim. Slov.
, vol.53
, pp. 210
-
-
Nagawade, R.R.1
Shinde, D.B.2
-
14
-
-
0034040349
-
A convenient method of synthesis of bis-indolylmethane: Indium trichloride-catalysed reactions of indole with aldehydes and Schiff's bases
-
Babu, G.; Sridhar, N.; Perumal, P. T. A convenient method of synthesis of bis-indolylmethane: Indium trichloride-catalysed 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
-
15
-
-
31044439253
-
Preparation of indolyl methanes catalyzed by metal hydrogen sulphates
-
Firouzabadi, H.; Iranpoor, N.; Ali Jafari, A. Preparation of indolyl methanes catalyzed by metal hydrogen sulphates. J. Mol. Cat. A: Chem. 2006, 244, 168.
-
(2006)
J. Mol. Cat. A: Chem.
, vol.244
, pp. 168
-
-
Firouzabadi, H.1
Iranpoor, N.2
Ali Jafari, A.3
-
16
-
-
0242351853
-
Efficient synthesis of bis(indolyl)methanes catalyzed by Lewis acids in ionic liquids
-
Shun, J. J.; Shun, W.-Y.; Yong, Z.; Teck, L.-P. Efficient synthesis of bis(indolyl)methanes catalyzed by Lewis acids in ionic liquids. Synlett 2003, 2077.
-
(2003)
Synlett
, pp. 2077
-
-
Shun, J.J.1
Shun, W.-Y.2
Yong, Z.3
Teck, L.-P.4
-
17
-
-
4544309609
-
A versatile and practical synthesis of bis-indolyl-methane=bis-indolyl glycoconjugates catalysed by trichloro-1,3,5-triazine
-
Sharma, G. V. M.; Reddy, J. J.; Lakshmi, P. S. A versatile and practical synthesis of bis-indolyl-methane=bis-indolyl glycoconjugates catalysed 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
-
18
-
-
2442680183
-
Potasium hydrogen sulphate-catalyzed reactions of indoles: A mild, expedient synthesis of bis-indolyl methanes
-
Nagarajan, R.; Perumal, P. T. Potasium hydrogen sulphate-catalyzed reactions of indoles: A mild, expedient synthesis of bis-indolyl methanes. Chem. Lett. 2004, 33, 288.
-
(2004)
Chem. Lett.
, vol.33
, pp. 288
-
-
Nagarajan, R.1
Perumal, P.T.2
-
19
-
-
45749105227
-
Lanthanum(III) nitrate hexahydrate: A versatile reagent for the synthesis of bis(indolyl) methanes under solvent-free conditions
-
Selvam, J.; Venkateswarlu, Y. Lanthanum(III) nitrate hexahydrate: A versatile reagent for the synthesis of bis(indolyl) methanes under solvent-free conditions. Synth. Commun. 2008, 38, 1760.
-
(2008)
Synth. Commun.
, vol.38
, pp. 1760
-
-
Selvam, J.1
Venkateswarlu, Y.2
-
20
-
-
41449113889
-
Facile synthesis of bis-indolyl-methanes catalyzed by ferric dodecyl sulfonate [Fe(DS) 3] in water at room temperature
-
Wang, S.-Y.; Ji, S.-J. Facile synthesis of bis-indolyl-methanes catalyzed by ferric dodecyl sulfonate [Fe(DS)3] in water at room temperature. Synth. Commun. 2008, 38, 1291.
-
(2008)
Synth. Commun.
, vol.38
, pp. 1291
-
-
Wang, S.-Y.1
Ji, S.-J.2
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