Copyright (c) 2018 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Green Synthesis of Bis(indolyl)methane Derivatives using PEG-400
Corresponding Author(s) : Bhaskar Kuthati
Asian Journal of Chemistry,
Vol. 30 No. 6 (2018): Vol 30 Issue 6
Abstract
Polyethylene glycol (PEG-400) has been considered as an effective and eco-friendly solvent cum activator for the one-pot coupling of indole and aldehydes to produce indole derivatives. The reaction was performed under mild conditions and the versatility of one-pot reaction was confirmed.
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References
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P.R. Singh, D.U. Singh and S.D. Samant, Synth. Commun., 35, 2133 (2005); https://doi.org/10.1080/00397910500180428.
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M.L. Kantam, K. Aziz and P.R. Likhar, Catal. Lett., 98, 117 (2004); https://doi.org/10.1007/s10562-004-7925-5.
L. Mo, Z. Ma and Z. Zhang, Synth. Commun., 35, 1997 (2005); https://doi.org/10.1081/SCC-200066653.
R.R. Nagawade and D.B. Shinde, Bull. Korean Chem. Soc., 26, 1962 (2005); https://doi.org/10.5012/bkcs.2005.26.12.1962.
K. Niknam, M.A. Zolfigol, T. Sadabadi and A. Nejati, J. Iran. Chem. Soc., 3, 318 (2006); https://doi.org/10.1007/BF03245953.
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G. Babu, N. Sridhar and P.T. Perumal, Synth. Commun., 30, 1609 (2000); https://doi.org/10.1080/00397910008087197.
B.P. Bandgar and K.A. Shaikh, J. Chem. Res. (S), 34 (2004); https://doi.org/10.3184/030823404323000701.
X.-L. Mi, S.-Z. Luo, J.-Q. He and J.-P. Cheng, Tetrahedron Lett., 45, 4567 (2004); https://doi.org/10.1016/j.tetlet.2004.04.039.
S.-J. Ji, M.-F. Zhou, D.-G. Gu, Z.-Q. Jiang and T.-P. Loh, Eur. J. Org. Chem., 1584 (2004); https://doi.org/10.1002/ejoc.200300719.
D. Chen, L. Yu and P.G. Wang, Tetrahedron Lett., 37, 4467 (1996); https://doi.org/10.1016/0040-4039(96)00958-6.
F. Shirini, A. Yahyazadeh, M. Abedini and D.I. Langroodi, Bull. Korean Chem. Soc., 31, 1715 (2010); https://doi.org/10.5012/bkcs.2010.31.6.1715.
M.A. Naik, D. Sachdev and A. Dubey, Catal. Commun., 11, 1148 (2010); https://doi.org/10.1016/j.catcom.2010.06.004.
R. Ghorbani-Vaghei, H. Veisi, H. Keypour and A.A. Dehghani-Firouzabadi, Mol. Divers., 14, 87 (2010); https://doi.org/10.1007/s11030-009-9150-z.
K. Niknam, D. Saberi and M. Baghernejad, Phosphorus Sulfur Silicon Rel. Elem., 185, 875 (2010); https://doi.org/10.1080/10426500903019127.
M.A. Zolfigol, A. Khazaei, A.R. Moosavi-Zare and A. Zare, Org. Prep. Proced. Int., 42, 95 (2010); https://doi.org/10.1080/00304940903585495.
L. Iglesias, C. Aguilar, D. Bandyopadhyay and B.K. Banik, Synth. Commun., 40, 3678 (2010); https://doi.org/10.1080/00397910903531631.
G. Meshram and V.D. Patil, Synth. Commun., 40, 29 (2009); https://doi.org/10.1080/00397910902916064.
E. Rafiee, Z. Zolfagharifar, M. Joshaghani and S. Eavani, Appl. Catal. A, 365, 287 (2009); https://doi.org/10.1016/j.apcata.2009.06.030.
A. Karam, J.C. Alonso, T.I. Gerganova, P. Ferreira, N. Bion, J. Barrault and F. Jérome, Chem. Commun., 7000 (2009); https://doi.org/10.1039/b914689j.
C.C. Silveira, S.R. Mendes, F.M. Líbero, E.J. Lenardão and G. Perin, Tetrahedron Lett., 50, 6060 (2009); https://doi.org/10.1016/j.tetlet.2009.08.062.
S. Chandrasekhar, S. Khatun, G. Rajesh and C.R. Reddy, Tetrahedron Lett., 50, 6693 (2009); https://doi.org/10.1016/j.tetlet.2009.09.085.
M.M. Heravi, K. Bakhtiari, A. Fatehi and F.F. Bamoharram, Catal. Commun., 9, 289 (2008); https://doi.org/10.1016/j.catcom.2007.07.039.
S.V. Nadkarni, M.B. Gawande, R.V. Jayaram and J.M. Nagarkar, Catal. Commun., 9, 1728 (2008); https://doi.org/10.1016/j.catcom.2008.01.036.
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P.T. Anastas and J.C. Warner, Green Chemistry Theory and Practice, Oxford University Press, Oxford (1998).
P.T. Anasta and T.C. Williamson, Green Chemistry Frontier in Benign Chemical Synthesis and Processes; Oxford University Press, Oxford (1998).
C. Christ, Production Integrated Environmental Protection and Waste Managements in the Chemical Industry, Wiley-VCH, Weinheim (1999).
Z.H. Zhang, L. Yin, Y.M. Wang, J.Y. Liu and Y. Li, Green Chem., 6, 563 (2004); https://doi.org/10.1039/b410583d.
V.K. Fulwa and V. Manivannan, Tetrahedron, 68, 3927 (2012); https://doi.org/10.1016/j.tet.2012.03.095.
L. Nagarapu, R. Mallepalli, U.N. Kumar, P. Venkateswarlu, R. Bantu and L. Yeramanchi, Tetrahedron Lett., 53, 1699 (2012); https://doi.org/10.1016/j.tetlet.2012.01.045.
B.S. Reddy, A. Naidu and P.K. Dubey, Green Chem. Lett. Rev., 6, 254 (2013); https://doi.org/10.1080/17518253.2012.742142.
P. Ramesh and K. Bhaskar, Asian J. Chem., 28, 2517 (2016); https://doi.org/10.14233/ajchem.2016.20061.
P. Ramesh and K. Bhaskar, Asian J. Org. Med. Chem., 2, 61 (2016); https://doi.org/10.14233/ajomc.2016.AJOMC-P18.
P. Ramesh and K. Bhaskar, Der Pharm. Lett., 8, 1 (2016).
Y.-H. Hui, Y.-C. Chen, H.-W. Gong and Z.-F. Xie, Chinese Chem. Lett., 25, 163 (2014); https://doi.org/10.1016/j.cclet.2013.09.010.
Z.-B. Xie, D.-Z. Sun, G.-F. Jiang and Z.-G. Le, Molecules, 19, 19665 (2014); https://doi.org/10.3390/molecules191219665.
T.M. Kubczyk, S.M. Williams, J.R. Kean, T.E. Davies, S.H. Taylor and A.E. Graham, Green Chem., 13, 2320 (2011); https://doi.org/10.1039/C1GC15669A.