-
1
-
-
0028334469
-
Stereocontrolled synthesis of (f)-hapalindole G
-
(a) Fukuyama, T.; Chen, X. J. Stereocontrolled synthesis of (f)-hapalindole G. J. Am. Chem. Soc. 1994, 116, 3125-3126;
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 3125-3126
-
-
Fukuyama, T.1
Chen, X.J.2
-
3
-
-
0025102581
-
Synthetic studies of marine alkaloids hapalindoles. Part 3. Total synthesis of (±)-hapalindoles H and U
-
DOI 10.1016/S0040-4020(01)96007-7
-
(c) Murakatake, H.; Kimagami, H.; Natsume, M. Synthetic studies of marine alkaloids hapalindoles, Part 3: Total synthesis of (r)-hapalindoles H and U. Tetrahedron 1990, 46, 6351-6360; (Pubitemid 20311620)
-
(1990)
Tetrahedron
, vol.46
, Issue.18
, pp. 6351-6360
-
-
Muratake, H.1
Kumagami, H.2
Natsume, M.3
-
4
-
-
77951219896
-
Bis-and trisindolylmethnanes (BIMS ans TIMS)
-
(d) Shiri, M.; Zolfigol, M.; Kruger, H. G.; Tanbakouchian, Z. Bis-and trisindolylmethnanes (BIMS ans TIMS). Chem. Rev. 2010, 110, 2250-2293.
-
(2010)
Chem. Rev.
, vol.110
, pp. 2250-2293
-
-
Shiri, M.1
Zolfigol, M.2
Kruger, H.G.3
Tanbakouchian, Z.4
-
5
-
-
0037087501
-
Bcl-2 family-mediated apoptotic effects of 3,3′-diindolylmethane (DIM) in human breast cancer cells
-
DOI 10.1016/S0006-2952(02)00856-0, PII S0006295202008560
-
Hong, C.; Firestone, G. L.; Bjelanes, L. F. Bcl-2 family-mediated apoptotic effects of 3,30-diindolylmethane (DIM) in human breast cancer cells. Biochem. Pharmacol. 2002, 63, 1085-1097. (Pubitemid 34267024)
-
(2002)
Biochemical Pharmacology
, vol.63
, Issue.6
, pp. 1085-1097
-
-
Hong, C.1
Firestone, G.L.2
Bjeldanes, L.F.3
-
6
-
-
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, 4719-4722.
-
(1983)
Tetrahedron Lett.
, vol.24
, pp. 4719-4722
-
-
Osawa, T.1
Namiki, M.2
-
7
-
-
31544464135
-
Inhibition of bladder tumor growth by 1,1-bis(3′-indolyl)-1-(p- substitutedphenyl)methanes: A new class of peroxisome proliferator-activated receptor γ agonists
-
DOI 10.1158/0008-5472.CAN-05-2755
-
Kassouf, W.; Chintharlapalli, S.; Abdelrahim, M.; Nelkin, G.; Safe, S.; Kamat, A. M. 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, 412-418. (Pubitemid 43166049)
-
(2006)
Cancer Research
, vol.66
, Issue.1
, pp. 412-418
-
-
Kassouf, W.1
Chintharlapalli, S.2
Abdelrahim, M.3
Nelkin, G.4
Safe, S.5
Kamat, A.M.6
-
8
-
-
0037016927
-
3 catalyzed reactions: Synthesis of 3-acetyl indoles, bis-indolylmethane and indolylquinoline derivatives
-
DOI 10.1016/S0040-4020(01)01227-3, PII S0040402001012273
-
Nagarajan, R.; Perumal, P. T. InCl3-and In(OTf)3-catalyzed reactions: Synthesis of 3-acetyl indoles, bis-indolylmethane, and indolylquinoline derivatives. Tetrahedron 2002, 58, 1229-1232. (Pubitemid 34112600)
-
(2002)
Tetrahedron
, vol.58
, Issue.6
, pp. 1229-1232
-
-
Nagarajan, R.1
Perumal, P.T.2
-
9
-
-
2342483570
-
Dy(OTf) 3 in ionic liquid: An efficient catalytic system for reactions of indole with aldehydes=ketones or imines
-
Mi, X. L.; Luo, S. Z.; He, J. Q.; Cheng, J. P. Dy(OTf)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
-
10
-
-
19944361904
-
3-catalyzed efficient synthesis of β,β- bis(indolyl) ketones by the double indolylation of acetic acid 2-methylene-3-oxobutyl estert
-
DOI 10.1039/b503378k
-
Ma, S.; Yu, S.; Peng, Z. Sc(OTf)3-catalyzed efficient synthesis of bis(indolyl) ketones by the double indolylation of acetic acid 2-methylene-3-oxobutyl ester. Org. Biomol. Chem. 2005, 3, 1933-1936. (Pubitemid 40751364)
-
(2005)
Organic and Biomolecular Chemistry
, vol.3
, Issue.10
, pp. 1933-1936
-
-
Ma, S.1
Yu, S.2
Peng, Z.3
-
11
-
-
0037463441
-
Molecular iodine-catalyzed efficient and highly rapid synthesis of bis(indolyl)methanes under mild conditions
-
DOI 10.1016/S0040-4039(03)00032-7, PII S0040403903000327
-
Bandagar, 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. (Pubitemid 36183442)
-
(2003)
Tetrahedron Letters
, vol.44
, Issue.9
, pp. 1959-1961
-
-
Bandgar, 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
-
DOI 10.1016/j.tetlet.2005.12.093, PII S0040403905027929
-
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, 1441-1443. (Pubitemid 43151159)
-
(2006)
Tetrahedron Letters
, vol.47
, Issue.9
, pp. 1441-1443
-
-
Deb, M.L.1
Bhuyan, P.J.2
-
13
-
-
33745949373
-
Spectrometric determination of pKa values for somephenolic compounds in acetonitrile-water mixture
-
Hakan, A. A.; Nurullah; Pekcan, G. Spectrometric determination of pKa values for somephenolic compounds in acetonitrile-water mixture. Acta. Chim. Slov. 2006, 53, 210-213.
-
(2006)
Acta. Chim. Slov.
, vol.53
, pp. 210-213
-
-
Hakan, A.A.1
Nurullah2
Pekcan, G.3
-
14
-
-
0034040349
-
A convenient method of synthesis of bisindolylmethanes: 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 indolyl methanes: Indium trichloride-catalyzed reactions of indole with aldehydes and schiff's bases. Synth. Commun. 2000, 30, 1609-1614. (Pubitemid 30205356)
-
(2000)
Synthetic Communications
, vol.30
, Issue.9
, pp. 1609-1614
-
-
Babu, G.1
Sridhar, N.2
Perumal, P.T.3
-
15
-
-
31044439253
-
40), a versatile and a highly water tolerant green Lewis acid catalyzes efficient preparation of indole derivatives
-
DOI 10.1016/j.molcata.2005.09.005, PII S1381116905006370
-
Firouzabadi, H.; Iranpoor, N.; Jafari, A. A. Aluminum dodecatungstophosphate (AlPW12O40), a versatile and a highly water-tolerant green Lewis acid catalyzes efficient preparation of indole derivatives. J. Mol. Cat. A: Chem. 2006, 244, 168-172. (Pubitemid 43121411)
-
(2006)
Journal of Molecular Catalysis A: Chemical
, vol.244
, Issue.1-2
, pp. 168-172
-
-
Firouzabadi, H.1
Iranpoor, N.2
Jafari, A.A.3
-
16
-
-
0242351853
-
Efficient synthesis of bis (indolyl methanes) catalysed by Lewis acids in ionic liquids
-
Ji, S. J.; Zhou, M. F.; Gu, D. G.; Wang, S. Y.; Loh, T. P. Efficient synthesis of bis (indolyl methanes) catalysed 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
-
17
-
-
4544309609
-
A versatile and practical synthesis of bis(indolyl)methanes/bis(indolyl) glycoconjugates catalyzed by trichloro-1,3,5-triazine
-
DOI 10.1016/j.tetlet.2004.08.084, PII S0040403904017952
-
Sharma, G. V. M.; Reddy, J. J.; Lakshmi, P. S. A versatile and practical synthesis of bis(indolyl)methanes=bis(indolyl)glycoconjugates catalyzed by trichloro-1,3,5-triazine. Tetrahedron Lett. 2004, 45, 7729-7732. (Pubitemid 39243360)
-
(2004)
Tetrahedron Letters
, vol.45
, Issue.41
, pp. 7729-7732
-
-
Sharma, G.V.M.1
Janardhan Reddy, J.2
Sree Lakshmi, P.3
Radha Krishna, P.4
-
18
-
-
2442680183
-
Potassium hydrogen sulfate-catalyzed reactions of indoles: A mild, expedient synthesis of bis-indolylmethanes
-
DOI 10.1246/cl.2004.288
-
Nagarajan, R.; Perumal, P. T. Potassium hydrogen sulfate-catalyzed reactions of indoles: A mild, expedient synthesis of bis-indolylmethanes. Chem. Lett. 2004, 33, 288-289. (Pubitemid 38661965)
-
(2004)
Chemistry Letters
, vol.33
, Issue.3
, pp. 288-289
-
-
Nagarajan, R.1
Perumal, P.T.2
-
19
-
-
31444448205
-
An efficient and clean synthesis of bis (indolyl)methanes in a protic solvent at room temperature
-
Mohit, L. D.; Pulak, J. B. An efficient and clean synthesis of bis (indolyl)methanes in a protic solvent at room temperature. Tetrahedron Lett. 2006, 47, 1441-1443.
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 1441-1443
-
-
Mohit, L.D.1
Pulak, J.B.2
-
20
-
-
5344239616
-
Lewis acid catalyzed electrophilic substitution of indole with aldehydes and Schiff's bases under microwave solvent-free irradiation
-
DOI 10.1081/SCC-200028611
-
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, 3175-3182. (Pubitemid 39350079)
-
(2004)
Synthetic Communications
, vol.34
, Issue.17
, pp. 3175-3182
-
-
Xia, M.1
Wang, S.-H.2
Yuan, W.-B.3
-
21
-
-
34547961672
-
A solvent-free protocol for facile condensation of indoles with carbonyl compounds using silica chloride as a new, highly efficient, and mild catalyst
-
DOI 10.1139/V07-051
-
Hasaninejad, A.; Zare, A.; Sharghi, H.; Shekouhy, M.; Khalifeh, R.; Ben, A. S.; Zare, A. R. M. A solvent-free protocol for condensation of indoles with carbonyl compounds using silica chloride as a new, highly efficient, and mild catalyst. Can. J. Chem. 2007, 85, 416-420. (Pubitemid 47265052)
-
(2007)
Canadian Journal of Chemistry
, vol.85
, Issue.6
, pp. 416-420
-
-
Hasaninejad, A.1
Zare, A.2
Sharghi, H.3
Shekouhy, M.4
Khalifeh, R.5
Beni, A.S.6
Zare, A.R.M.7
-
22
-
-
34547607567
-
P2O5=SiO2 as an efficient, mild, and heterogeneous catalytic system for the condensation of indoles with carbonyl compounds under solvent-free condensations
-
Hasaninejad, A.; Zare, A.; Sharghi, H.; Niknam, K.; Shekouhy, M. P2O5=SiO2 as an efficient, mild, and heterogeneous catalytic system for the condensation of indoles with carbonyl compounds under solvent-free condensations. Arkivoc 2007, 39-50.
-
(2007)
Arkivoc
, pp. 39-50
-
-
Hasaninejad, A.1
Zare, A.2
Sharghi, H.3
Niknam, K.4
Shekouhy, M.5
-
23
-
-
39749096607
-
Trityl chloride as a novel and efficient organic atalyst for room temperature preparation of bis(indolyl) methanes under solvent-free conditions in neutral media
-
Khalafi Nazhad, A.; Parhami, A.; Zare, A.; Moosavi Zare, A. R.; Haraninejad, A.; Panahi, F. Trityl chloride as a novel and efficient organic atalyst for room temperature preparation of bis(indolyl) methanes under solvent-free conditions in neutral media. Synthesis 2008, 4, 617-621.
-
(2008)
Synthesis
, vol.4
, pp. 617-621
-
-
Khalafi Nazhad, A.1
Parhami, A.2
Zare, A.3
Zare, M.R.A.4
Haraninejad, A.5
Panahi, F.6
-
24
-
-
67650723297
-
An eco-friendly procedure for the efficient synthesis of bis(indolyl) methanes in aqueous media
-
Sobhani, S.; Safaei, E.; Hasaninejad, A. R.; Rezazadeh, S. An eco-friendly procedure for the efficient synthesis of bis(indolyl) methanes in aqueous media. J. Organomet. Chem. 2009, 694, 3027-3031.
-
(2009)
J. Organomet. Chem.
, vol.694
, pp. 3027-3031
-
-
Sobhani, S.1
Safaei, E.2
Hasaninejad, A.R.3
Rezazadeh, S.4
-
25
-
-
42449137901
-
Magnesium sulfate as an efficient and very cheap reagent for the preparation of bis (indolyl) methane
-
Hasaninejad, A.; Parhami, A.; Zare, A.; Khalafi Nezhad, A.; Shirazi, A. N.; Zare, A. R. M. Magnesium sulfate as an efficient and very cheap reagent for the preparation of bis (indolyl) methane. Pol. J. Chem. 2008, 82, 565-569.
-
(2008)
Pol. J. Chem.
, vol.82
, pp. 565-569
-
-
Hasaninejad, A.1
Parhami, A.2
Zare, A.3
Khalafi Nezhad, A.4
Shirazi, A.N.5
Zare, A.R.M.6
-
26
-
-
0032546116
-
Polyethylene glycol (PEG) as polymeric support and phase-transfer catalyst in the soluble polymer liquid phase synthesis of α-amino esters
-
DOI 10.1016/S0040-4039(97)10722-5, PII S0040403997107225
-
Sauvagnat, B.; Lamaty, F.; Lazro, R.; Martinez, J. Polyethylene glycol (PEG) as polymeric support and phase-transfer catalyst in the soluble polymer liquid-phase synthesis of a-amino esters. Tetrahedron Lett. 1998, 39, 821-824. (Pubitemid 28055347)
-
(1998)
Tetrahedron Letters
, vol.39
, Issue.8
, pp. 821-824
-
-
Sauvagnat, B.1
Lamaty, F.2
Lazaro, R.3
Martinez, J.4
-
27
-
-
31744432111
-
3H as catalyst for 3,4-dihydropyrimidones via Biginelli reaction under microwave and solvent-free conditions
-
DOI 10.1080/00397910500383519, PII RH466368L7M22442
-
(a) Wang, X.; Quan, Z.; Wang, F.; Wang, M.; Zhang, L. PEG-SO3H as catalyst for 3,4-dihydropyrimidones via Biginelli reaction under microwave and solvent-free conditions. Synth. Commun. 2006, 36, 451-456; (Pubitemid 43175901)
-
(2006)
Synthetic Communications
, vol.36
, Issue.4
, pp. 451-456
-
-
Wang, X.1
Quan, Z.2
Wang, F.3
Wang, M.4
Zhang, Z.5
Li, Z.6
-
28
-
-
50649094669
-
PEG-SO3H as soluble acidic polymeric catalyst for regioselective ring opening of epoxides: A highefficiency synthetic approach to b-hydroxy thiocynates
-
(b) Kisat, A. K.; Mehrjardi, M. F. PEG-SO3H as soluble acidic polymeric catalyst for regioselective ring opening of epoxides: A highefficiency synthetic approach to b-hydroxy thiocynates. Synth. Commun. 2008, 38, 2995-3002;
-
(2008)
Synth. Commun.
, vol.38
, pp. 2995-3002
-
-
Kisat, A.K.1
Mehrjardi, M.F.2
-
29
-
-
67349148913
-
PEG-SO3H as catalyst for the Beckmann rearrangement and dehydration of oximes
-
(c) Wang, X. C.; Li, L.; Quan, Z. J.; Gong, H. P.; Ye, H. L.; Cao, X. F. PEG-SO3H as catalyst for the Beckmann rearrangement and dehydration of oximes. Chin. Chem. Lett. 2009, 20, 651-655;
-
(2009)
Chin. Chem. Lett.
, vol.20
, pp. 651-655
-
-
Wang, X.C.1
Li, L.2
Quan, Z.J.3
Gong, H.P.4
Ye, H.L.5
Cao, X.F.6
-
30
-
-
39549111678
-
PEG-SO3H as eco-friendly polymeric catalyst for regioselective ring opening of epoxides using thiocyanate anion in water: An efficient route to synthesis of b-hydroxy thiocyanate
-
(d) Kisat, A. K.; Mehrjardi, M. F. PEG-SO3H as eco-friendly polymeric catalyst for regioselective ring opening of epoxides using thiocyanate anion in water: An efficient route to synthesis of b-hydroxy thiocyanate. Catal. Commun. 2008, 9, 1497-1500;
-
(2008)
Catal. Commun.
, vol.9
, pp. 1497-1500
-
-
Kisat, A.K.1
Mehrjardi, M.F.2
-
31
-
-
61849181999
-
PS-PEGSO3H as an efficient catalyst for 3,4-dihydropyrimidones via Biginelli reaction
-
(e) Quan, Z.-J.; Da, Y.-X.; Zang, Z., Wang, X. C. PS-PEGSO3H as an efficient catalyst for 3,4-dihydropyrimidones via Biginelli reaction. Catal. Commun. 2009, 10, 1146-1148.
-
(2009)
Catal. Commun.
, vol.10
, pp. 1146-1148
-
-
Quan, Z.-J.1
Da, Y.-X.2
Zang, Z.3
Wang, X.C.4
-
32
-
-
2442492149
-
Synthesis and characterization of bis(indolyl) methanes, tris(indolyl)methane, and new diindolylcarzolylmethanes mediated by Zeokarb-225, a novel, recyclable, eco-benign heterogenous catalyst
-
Magesh, C. J.; Rajagopal, A.; Karthik, M. Synthesis and characterization of bis(indolyl) methanes, tris(indolyl)methane, and new diindolylcarzolylmethanes mediated by Zeokarb-225, a novel, recyclable, eco-benign heterogenous catalyst. Appl. Catal. A 2004, 266, 1-10.
-
(2004)
Appl. Catal. A
, vol.266
, pp. 1-10
-
-
Magesh, C.J.1
Rajagopal, A.2
Karthik, M.3
-
33
-
-
84897571107
-
Synthesis of bis(indolyl) methanes using recyclable PEG-supported sulfonic acid as catalyst
-
Sheng, S.-R.; Wang, Q.-Y.; Dang, Y.; Liu, Y.-L.; Cai, M.-Z. Synthesis of bis(indolyl) methanes using recyclable PEG-supported sulfonic acid as catalyst. Catal. Lett. 2009, 128, 418-422.
-
(2009)
Catal. Lett.
, vol.128
, pp. 418-422
-
-
Sheng, S.-R.1
Wang, Q.-Y.2
Dang, Y.3
Liu, Y.-L.4
Cai, M.-Z.5
-
34
-
-
70349777320
-
Alum-catalyzed simple and efficient synthesis of bis(indolyl)methane by ultrasound approach
-
Sonar, S. S.; Sadaphal, S. A.; Kategaonkar, A. H.; Pokalwar, R. U.; Shingate, B. B.; Shingare, M. S. Alum-catalyzed simple and efficient synthesis of bis(indolyl)methane by ultrasound approach. Bull. Korean Chem. Soc. 2009, 30, 825-828.
-
(2009)
Bull. Korean Chem. Soc.
, vol.30
, pp. 825-828
-
-
Sonar, S.S.1
Sadaphal, S.A.2
Kategaonkar, A.H.3
Pokalwar, R.U.4
Shingate, B.B.5
Shingare, M.S.6
-
35
-
-
33845984969
-
A new catalytic method for the preparation of bis-indolyl and tris-indolyl methanes in aqueous media
-
DOI 10.1016/j.catcom.2006.06.012, PII S1566736706002147
-
Zolfigol, M. A.; Salchi, S. P.; Shiri, M.; Tanbakouchian, Z. A new catalytic method for the preparation of bis-indolyl methanes and tris-indolyl methanes in aqueous media. Catal. Commun. 2007, 8, 173-178. (Pubitemid 46043569)
-
(2007)
Catalysis Communications
, vol.8
, Issue.2
, pp. 173-178
-
-
Zolfigol, M.A.1
Salehi, P.2
Shiri, M.3
Tanbakouchian, Z.4
-
36
-
-
57749196357
-
A mild and versatile synthesis of bis(indolyl)methanes and tris(indolyl) alkanes ctalised by antimony trichloride
-
Kundu, P.; Maiti, G. A mild and versatile synthesis of bis(indolyl)methanes and tris(indolyl) alkanes ctalised by antimony trichloride. Indian J. Chem. 2008, 47B, 1402-1406.
-
(2008)
Indian J. Chem.
, vol.47 B
, pp. 1402-1406
-
-
Kundu, P.1
Maiti, G.2
|