-
1
-
-
0028605225
-
Vibrindole A: A metabolite of the marine bacterium, vibrio parahaemolyticus, isolated from the toxic mucus of the boxfish ostracion cubicus
-
(a) Bell, R.; Carmeli, S.; Sar, N. Vibrindole A: A metabolite of the marine bacterium, vibrio parahaemolyticus, isolated from the toxic mucus of the boxfish ostracion cubicus. J. Nat. Prod. 1994, 57, 1587-1590;
-
(1994)
J. Nat. Prod.
, vol.57
, pp. 1587-1590
-
-
Bell, R.1
Carmeli, S.2
Sar, N.3
-
2
-
-
0025998158
-
6-Bromotryptamine derivatives from the gulf of California tunicate didemnum candidum
-
(b) Fahy, E.; Porn, B. C. M.; Faulkner, D. J.; Smith, K. 6-Bromotryptamine derivatives from the gulf of California tunicate didemnum candidum. J. Nat. Prod. 1991, 54, 564-569;
-
(1991)
J. Nat. Prod.
, vol.54
, pp. 564-569
-
-
Fahy, E.1
Porn, B.C.M.2
Faulkner, D.J.3
Smith, K.4
-
3
-
-
0034041015
-
Indolyl carboxylic acids by condensation of indoles with α-keto acidc
-
(c) Garbe, T. R.; Kobayashi, M.; Shimizu, N.; Takesue, N.; Ozawa, M.; Yukawa, H. Indolyl carboxylic acids by condensation of indoles with α-keto acidc. J. Nat. Prod. 2000 (63), 596-598.
-
(2000)
J. Nat. Prod.
, vol.63
, pp. 596-598
-
-
Garbe, T.R.1
Kobayashi, M.2
Shimizu, N.3
Takesue, N.4
Ozawa, M.5
Yukawa, H.6
-
5
-
-
0030297325
-
3,3′-diindolylmethane induces apoptosis in human cancer cells
-
Ge, X.; Yannai, S.; Rennert, G.; Gruener, N.; Fares, F. A. 3,3′-Diindolylmethane induces apoptosis in human cancer cells. Biochem. Biophys. Res. Commun. 1996, 228, 153-158.
-
(1996)
Biochem. Biophys. Res. Commun.
, vol.228
, pp. 153-158
-
-
Ge, X.1
Yannai, S.2
Rennert, G.3
Gruener, N.4
Fares, F.A.5
-
6
-
-
0035691856
-
A sojourn in the synthesis and bioactivity of diindolylalkanes
-
Chakrabarty, M.; Basak, R.; Harigaya, Y. A sojourn in the synthesis and bioactivity of diindolylalkanes. Heterocycles 2001, 55, 2431-2447.
-
(2001)
Heterocycles
, vol.55
, pp. 2431-2447
-
-
Chakrabarty, M.1
Basak, R.2
Harigaya, Y.3
-
7
-
-
3943087054
-
Synthesis of some substituted di-indolylmethanes in aqueous medium at room temperature
-
Kamal, A.; Qureshi, A. A. Synthesis of some substituted di-indolylmethanes in aqueous medium at room temperature. Tetrahedron 1963, 19, 513-520.
-
(1963)
Tetrahedron
, vol.19
, pp. 513-520
-
-
Kamal, A.1
Qureshi, A.A.2
-
8
-
-
0034040349
-
A convenient method of synthesis of bis-indolylmethanes: Indium trichloride-catalysed reactions of indole with aldehydes and Schiffs bases
-
Babu, G.; Sridhar, N.; Perumal, P. T. A convenient method of synthesis of bis-indolylmethanes: Indium trichloride-catalysed reactions of indole with aldehydes and Schiffs bases. Synth. Commun. 2000, 30, 1609-1614.
-
(2000)
Synth. Commun.
, vol.30
, pp. 1609-1614
-
-
Babu, G.1
Sridhar, N.2
Perumal, P.T.3
-
9
-
-
0037016927
-
3-catalyzed reaction: Synthesis of 3-acetyl indoles, bis-indolymethane and indolyquinoline derivatives
-
3-catalyzed reaction: Synthesis of 3-acetyl indoles, bis-indolymethane and indolyquinoline derivatives. Tetrahedron 2002, 58, 1229-1232.
-
(2002)
Tetrahedron
, vol.58
, pp. 1229-1232
-
-
Nagarajan, R.1
Perumal, P.T.2
-
10
-
-
1842450325
-
3 catalysed synthesis of bis(indolyl)methanes in water under mild conditions
-
3 catalysed synthesis of bis(indolyl)methanes in water under mild conditions. J. Chem. Res. Synop. 2004, 34-36.
-
(2004)
J. Chem. Res. Synop.
, pp. 34-36
-
-
Bandgar, B.P.1
Shaikh, K.A.2
-
11
-
-
2342483570
-
3 in ionic liquid: An efficient catalytic system for reactions of indole with aldehydes/ketones or imines
-
3 in ionic liquid: An efficient catalytic system for reactions of indole with aldehydes/ketones or imines. Tetrahedron Lett. 2004, 45, 4567-4570.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 4567-4570
-
-
Mi, X.-L.1
Luo, S.-Z.2
He, J.-Q.3
Cheng, J.-P.4
-
12
-
-
0030600171
-
Lewis acid-catalyzed reactions in protic media. Lanthanide-catalyzed reactions of indoles with aldehydes or ketones
-
Chen, D.; Yu, L.; Wang, P. G. Lewis acid-catalyzed reactions in protic media. Lanthanide-catalyzed reactions of indoles with aldehydes or ketones. Tetrahedron Lett. 1996, 37, 4467-4470.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 4467-4470
-
-
Chen, D.1
Yu, L.2
Wang, P.G.3
-
13
-
-
0035042642
-
Lithium perchlorate-catalysed ractions of indoles: An expeditious synthesis of bis(indolyl)methanes
-
Yadav, J. S.; Reddy, B. V. S.; Murthy, Ch. V. S. R.; Kumar, G. M.; Madan, Ch. Lithium perchlorate-catalysed ractions of indoles: An expeditious synthesis of bis(indolyl)methanes. Synthesis 2001, 783-787.
-
(2001)
Synthesis
, pp. 783-787
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Murthy, Ch.V.S.R.3
Kumar, G.M.4
Madan, Ch.5
-
14
-
-
5344239616
-
Lewis acid-catalyzed electrophilic substitution of indole with aldehydes and Schiffs bases under microwave solvent-free irradiation
-
Xia, M.; Wang, S.-B.; Yuan, W.-B. Lewis acid-catalyzed electrophilic substitution of indole with aldehydes and Schiffs bases under microwave solvent-free irradiation. Synth. Commun. 2004, 34, 3175-3182.
-
(2004)
Synth. Commun.
, vol.34
, pp. 3175-3182
-
-
Xia, M.1
Wang, S.-B.2
Yuan, W.-B.3
-
15
-
-
1042298780
-
Facile synthesis of bis(indolyl)-methanes using catalytic amount of iodine at room temperature under solvent-free conditions
-
(a) 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, 2051-2055;
-
(2004)
Tetrahedron
, vol.60
, pp. 2051-2055
-
-
Ji, S.-J.1
Wang, S.-Y.2
Zhang, Y.3
Loh, T.-P.4
-
16
-
-
0037463441
-
Molecular iodine-catalyzed efficient and highly rapid synthesis of bis(indolyl)methanes under mild conditions
-
(b) Bandgar, B. P.; Shaikh, K. A. Molecular iodine-catalyzed efficient and highly rapid synthesis of bis(indolyl)methanes under mild conditions. Tetrahedron Lett. 2003, 44, 1959-1961.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 1959-1961
-
-
Bandgar, B.P.1
Shaikh, K.A.2
-
17
-
-
0036745995
-
N-Bromosuccinimide-catalyzed condensations of indoles with carbonyl compounds under solvent-free conditions
-
Koshima, H.; Matsuaka, W. N-Bromosuccinimide-catalyzed condensations of indoles with carbonyl compounds under solvent-free conditions. J. Heterocycl. Chem. 2002, 39, 1089-1091.
-
(2002)
J. Heterocycl. Chem.
, vol.39
, pp. 1089-1091
-
-
Koshima, H.1
Matsuaka, W.2
-
18
-
-
2442680183
-
Potassium hydrogen sulfate-catalyzed reactions of indoes: A mild, expedient synthesis of bis-indlylmethanes
-
Nagarajan, R.; Perumal, P. T. Potassium hydrogen sulfate-catalyzed reactions of indoes: A mild, expedient synthesis of bis-indlylmethanes. Chem. Lett. 2004, 33, 288-289.
-
(2004)
Chem. Lett.
, vol.33
, pp. 288-289
-
-
Nagarajan, R.1
Perumal, P.T.2
-
19
-
-
0242573177
-
Silica-supported sodium hydrogen sulfate and amberlyst-15: Two efficient heterogenes catalysts for facile synthesis of bis- And tris(1H-indol-3-yl) methanes from indoles and carbonyl compounds
-
Ramesh, C.; Baneree, J.; Pal, R.; Das, B. Silica-supported sodium hydrogen sulfate and amberlyst-15: Two efficient heterogenes catalysts for facile synthesis of bis- and tris(1H-indol-3-yl)methanes from indoles and carbonyl compounds. Adv. Synth. Catal. 2003, 345, 557-559.
-
(2003)
Adv. Synth. Catal.
, vol.345
, pp. 557-559
-
-
Ramesh, C.1
Baneree, J.2
Pal, R.3
Das, B.4
-
20
-
-
0036166575
-
Electrophilic substition of indoles catalysed by triphenyl phoponium perchlorate: Synthesis of 3-acetyl indoles and bis-indolyl-methane derivatives
-
Nagarajan, R.; Perumal, P. T. Electrophilic substition of indoles catalysed by triphenyl phoponium perchlorate: Synthesis of 3-acetyl indoles and bis-indolyl-methane derivatives. Synth. Commun. 2002, 32, 105-109.
-
(2002)
Synth. Commun.
, vol.32
, pp. 105-109
-
-
Nagarajan, R.1
Perumal, P.T.2
-
21
-
-
0037628959
-
Electrophilic substitution reactions of indoles with carbonyl compounds usng ceric ammonium nitrate: A novel and efficient method for the synthesis of di- and tri-indolylmethanes
-
Ramesh, C.; Ravindranath, N.; Das, B. Electrophilic substitution reactions of indoles with carbonyl compounds usng ceric ammonium nitrate: A novel and efficient method for the synthesis of di- and tri-indolylmethanes. J. Chem. Res. Synop. 2003, 72-74.
-
(2003)
J. Chem. Res. Synop.
, pp. 72-74
-
-
Ramesh, C.1
Ravindranath, N.2
Das, B.3
-
22
-
-
2942559219
-
Zeolite-catalyzed electrophilic substitution reactions of indoles with aldehydes: Synthesis of bis(indolyl)methanes
-
(a) Karthik, M.; Tripathi, A. K.; Gupta, N. M.; Palanichamy, M.; Murugesan, V. Zeolite-catalyzed electrophilic substitution reactions of indoles with aldehydes: Synthesis of bis(indolyl)methanes. Catal. Commn. 2004, 5, 371-375;
-
(2004)
Catal. Commn.
, vol.5
, pp. 371-375
-
-
Karthik, M.1
Tripathi, A.K.2
Gupta, N.M.3
Palanichamy, M.4
Murugesan, V.5
-
23
-
-
0242268029
-
Zeolite-catalyzed synthesis of bis(indolyl)methanes
-
(b) Reddy, A. V.; Ravinder, K.; Reddy, V. L. N.; Goud, T. V.; Ravikanth, V.; Venkateseswarlu, Y. Zeolite-catalyzed synthesis of bis(indolyl)methanes. Synth. Commun. 2003, 33, 3687-3694.
-
(2003)
Synth. Commun.
, vol.33
, pp. 3687-3694
-
-
Reddy, A.V.1
Ravinder, K.2
Reddy, V.L.N.3
Goud, T.V.4
Ravikanth, V.5
Venkateseswarlu, Y.6
-
24
-
-
0037182271
-
Dry reaction of indoles with carbonyl compounds on montmorillonite K10 clay: A mild, expedient synthesis of diindolylalkanes and vibrindole A
-
(a) Chakrabarty, M.; Gosh, N.; Basak, R.; Harigaya, Y. Dry reaction of indoles with carbonyl compounds on montmorillonite K10 clay: A mild, expedient synthesis of diindolylalkanes and vibrindole A. Tetrahedron Lett. 2002, 43, 4075-4078;
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 4075-4078
-
-
Chakrabarty, M.1
Gosh, N.2
Basak, R.3
Harigaya, Y.4
-
25
-
-
0242606991
-
Infrared-assisted eco-friendly selective synthesis of diindolylmethanes
-
(b) Penieres-Carrillo, G.; García-Estrada, J. G.; Gutiérrez-Ramírez, J. L.; Alvarez-Toledano, C. Infrared-assisted eco-friendly selective synthesis of diindolylmethanes. Green Chem. 2003, 5, 337-339.
-
(2003)
Green Chem.
, vol.5
, pp. 337-339
-
-
Penieres-Carrillo, G.1
García-Estrada, J.G.2
Gutiérrez- Ramírez, J.L.3
Alvarez-Toledano, C.4
-
26
-
-
9744285166
-
An efficient procedure for the preparation of mono- and di-bis-indolyl methanes catalyzed by molibdatophosphoric acid
-
Zolfigol, M. A.; Salehi, P.; Shirl, 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, 2273-2277.
-
(2004)
Phosphorus, Sulfur Silicon Relat. Elem.
, vol.179
, pp. 2273-2277
-
-
Zolfigol, M.A.1
Salehi, P.2
Shirl, M.3
-
27
-
-
0242607159
-
Efficient and eco-friendly process for the synthesis of bis(1H-indol-3-yl)methanes using ionic liquids
-
Yadav, J. S.; Reddy, B. V. S.; Sunitha, S. Efficient and eco-friendly process for the synthesis of bis(1H-indol-3-yl)methanes using ionic liquids. Adv. Synth. Catal. 2003, 345, 349-352.
-
(2003)
Adv. Synth. Catal.
, vol.345
, pp. 349-352
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Sunitha, S.3
-
29
-
-
4544309609
-
A versatile and practical synhesis of bis(indoyl)methanes/bis(indolyl) glycoconjugates catalyzed by trichloro01,3-5-triazine
-
Sharma, G. V. M.; Reddy, J. J.; Lakshmi, P. S.; Krishna, P. R. A versatile and practical synhesis of bis(indoyl)methanes/bis(indolyl) glycoconjugates catalyzed by trichloro01,3-5-triazine. Tetrahedron Lett. 2004, 45, 7729-7732.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 7729-7732
-
-
Sharma, G.V.M.1
Reddy, J.J.2
Lakshmi, P.S.3
Krishna, P.R.4
-
30
-
-
7044234960
-
Hexamethylenetetraamine-bromine-catalyzed rapid and efficient synthesis of bis(indolyl)methanes
-
Bandgar, B. P.; Bettigeri, S. V.; Joshi, N. S. Hexamethylenetetraamine- bromine-catalyzed rapid and efficient synthesis of bis(indolyl)methanes. Monatsh. Chem. 2004, 135, 1265-1273.
-
(2004)
Monatsh. Chem.
, vol.135
, pp. 1265-1273
-
-
Bandgar, B.P.1
Bettigeri, S.V.2
Joshi, N.S.3
-
31
-
-
1542285883
-
Ion exchange resin-catalyzed condensation of indole and carbonyl compounds-synthesis of bis-indolylmethanes
-
Feng, X.-L.; Guan, C.-J.; Zhao, C.-X. Ion exchange resin-catalyzed condensation of indole and carbonyl compounds-Synthesis of bis-indolylmethanes. Synth. Commun. 2004, 34, 487-492.
-
(2004)
Synth. Commun.
, vol.34
, pp. 487-492
-
-
Feng, X.-L.1
Guan, C.-J.2
Zhao, C.-X.3
-
32
-
-
0242351853
-
Efficient synthesis of bis(indolyl)methanes catalyzed by Lewis acids in ionic liquids
-
(a) Ji, S.-J.; Zhou, M.-F.; Gu, D.-G.; Wang, S.-Y.; Loh, T.-P. Efficient synthesis of bis(indolyl)methanes catalyzed by Lewis acids in ionic liquids. Synlett 2003, 2077-2079;
-
(2003)
Synlett
, pp. 2077-2079
-
-
Ji, S.-J.1
Zhou, M.-F.2
Gu, D.-G.3
Wang, S.-Y.4
Loh, T.-P.5
-
34
-
-
0347357688
-
Selective bromination with copper(II) bromide
-
(a) King, L. C.; Ostrum, G. K. Selective bromination with copper(II) bromide. J. Org. Chem. 1964, 29, 3459-3461;
-
(1964)
J. Org. Chem.
, vol.29
, pp. 3459-3461
-
-
King, L.C.1
Ostrum, G.K.2
-
35
-
-
3042968942
-
Reactions of some organic compounds with cupric bromide
-
(b) Fort, A. W. Reactions of some organic compounds with cupric bromide. J. Org. Chem. 1961, 26, 765-767;
-
(1961)
J. Org. Chem.
, vol.26
, pp. 765-767
-
-
Fort, A.W.1
-
36
-
-
4644227875
-
Bromination of 17-oxo steroids with cupric bromide
-
(c) Glazier, E. R. Bromination of 17-oxo steroids with cupric bromide. J. Org. Chem. 1962, 27, 2937-2938;
-
(1962)
J. Org. Chem.
, vol.27
, pp. 2937-2938
-
-
Glazier, E.R.1
-
37
-
-
0242320438
-
2-mediated halogenation of alkylidenecyclopropanes: A highly efficient and stereo-selective method for the preparation of Z-2,4-dihalobutenes
-
2-mediated halogenation of alkylidenecyclopropanes: A highly efficient and stereo-selective method for the preparation of Z-2,4-dihalobutenes. Synlett 2003, 2080-2082.
-
(2003)
Synlett
, pp. 2080-2082
-
-
Zhou, H.W.1
Huang, X.2
Chen, W.L.3
-
38
-
-
0010589993
-
Reaction of cycloalkanones with copper(II) halide. III. Reaction of cyclohexanones and steroidal ketones with copper(II) halide in ethylene glycol
-
(a) Satoh, J. Y.; Yokoyama, C. T.; Haruta, A. M. Reaction of cycloalkanones with copper(II) halide. III. Reaction of cyclohexanones and steroidal ketones with copper(II) halide in ethylene glycol. Chem. Lett. 1974, 1521-1522;
-
(1974)
Chem. Lett.
, pp. 1521-1522
-
-
Satoh, J.Y.1
Yokoyama, C.T.2
Haruta, A.M.3
-
39
-
-
4143139730
-
Room temperature aerobic copper-catalysed selective oxidation of primary alcohols to aldehydes
-
(b) Gamez, P.; Arends, I. W. C. E.; Sheldon, R. A.; Reedijk, J. Room temperature aerobic copper-catalysed selective oxidation of primary alcohols to aldehydes. Adv. Synth. Catal. 2004, 346, 805-811.
-
(2004)
Adv. Synth. Catal.
, vol.346
, pp. 805-811
-
-
Gamez, P.1
Arends, I.W.C.E.2
Sheldon, R.A.3
Reedijk, J.4
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