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This work is licensed under a Creative Commons Attribution 4.0 International License.
Indium Metal-Induced Reactions: Synthesis of Biologically Active Molecules
Corresponding Author(s) : Bimal Krishna Banik
Asian Journal of Chemistry,
Vol. 30 No. 1 (2018): Vol 30 Issue 1
Abstract
Indium metal has proven to be extremely useful in our research for the synthesis of diverse organic compounds of significant importance.
Keywords
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- (a) B.K. Banik, A. Ghatak and F.F. Becker, J. Chem. Soc., Perkin Trans. 1, 2179 (2000); https://doi.org/10.1039/b002833i. (b) A. Ghatak, F.F. Becker and B.K. Banik, Heterocycles, 53, 2769 (2000); https://doi.org/10.3987/COM-00-9019. (c) S. Chandra, R.N. Yadav, L. Lareeb and B.K. Banik, Chem. Educ., 20,4 (2015).
- A. Ghatak and B.K. Banik, Heterocycl. Lett., 1, 99 (2011).
- (a) B.K. Banik, Heterocyclic Scaffolds I, Topics in Heterocyclic Chemistry, Springer, vol. 22, pp. 1-379 (2010). (b) B.K. Banik, β-Lactams: Synthesis and Biological Evaluation, Topics in Heterocyclic Chemistry, Springer, vol. 30, pp. 1-226 (2012). (c) B.K. Banik, Tetrahedron, 68, 10627 (2012); https://doi.org/10.1016/S0040-4020(12)01701-2. (d) I. Banik and B.K. Banik, Microwave-Induced Chemical Manipulation of β-Lactam, Topics in Heterocyclic Chemistry, Springer, vol. 88, pp. 781-1007 (2012). (e) B.K. Banik, Beta Lactams: Novel Synthetic Pathways and Applications, Springer, pp. 1-419 (2017). (f) P.T. Parvatkar, P.S. Parameswaran and B.K. Banik, ed.: B.K. Banik Solid Phase Synthesis of β-Lactams: Results and Scope; In: Beta Lactams: Novel Synthetic Pathways and Applications, Ed. Spinger, pp. 253-284 (2017). (g) S. Basu and B.K. Banik, ed.: B.K. Banik, Beta Lactams as Clinically Active Molecules, In: Beta Lactams: Novel Synthetic Pathways and Applications, Springer, pp. 285-310 (2017). (h) B.K. Banik, Synthesis and Biological Studies of Novel β-Lactams, CRC Book, pp. 31-72 (2013).
- (a) B.K. Banik, S. Samajdar, I. Banik, O. Zegrocka and F.F. Becker, Heterocycles, 55, 227 (2001); https://doi.org/10.3987/COM-00-9100. (b) I. Banik, S. Samajdar and B.K. Banik, Heterocycl. Lett., 1, 47 (2011).
- S. Samajdar, I. Banik and B.K. Banik, Heterocycl. Lett., 1, 41 (2011).
- B.K. Banik, S. Samajdar and F.F. Becker, Mol. Med. Rep., 3, 319 (2010); https://doi.org/10.3892/mmr_00000259.
- (a) I. Banik, F.F. Becker and B.K. Banik, J. Med. Chem., 46, 12 (2003); https://doi.org/10.1021/jm0255825. (b) B.K. Banik, I. Banik and L. Hackfeld, Heterocycles, 59, 505 (2003); https://doi.org/10.3987/COM-02-S76. (c) B.K. Banik, F.F. Becker and I. Banik, Bioorg. Med. Chem., 12, 2523 (2004); https://doi.org/10.1016/j.bmc.2004.03.033. (d) B.K. Banik, Curr. Med. Chem., 11, 1 (2012); https://doi.org/10.2174/0929867043364892. (e) B.K. Banik, I. Banik and F.F. Becker, Bioorg. Med. Chem., 13, 3611 (2005); https://doi.org/10.1016/j.bmc.2005.03.044. (f) B.K. Banik and F.F. Becker, Mol. Med. Rep., 3, 315 (2010); https://doi.org/10.3892/mmr_00000257. (g) B.K. Banik, I. Banik and F.F. Becker, Eur. J. Med. Chem., 45, 846 (2010); https://doi.org/10.1016/j.ejmech.2009.11.024. (h) B.K. Banik, Int. Innov., 50 (2011). (i) B.K. Banik, Int. Innov., 114 (2012).
- (a) B.K. Banik, M.S. Manhas and A.K. Bose, Tetrahedron Lett., 38, 5077 (1997); https://doi.org/10.1016/S0040-4039(97)01130-1. (b) B.K. Banik, O. Zegrocka, M.S. Manhas and A.K. Bose, Heterocycles, 46, 173 (1997); https://doi.org/10.3987/COM-97-S66. (c) B.K. Banik, M.S. Manhas and A.K. Bose, J. Org. Chem., 59, 4714 (1994); https://doi.org/10.1021/jo00096a004. (d) B.K. Banik, O. Zegrocka, M.S. Manhas and A.K. Bose, Heterocycles, 78, 2443 (2009); https://doi.org/10.3987/COM-09-11729. (e) B.K. Banik and M.S. Manhas, Tetrahedron, 68, 10769 (2012); https://doi.org/10.1016/j.tet.2012.01.078.
- (a) B.K. Banik, M. Suhendra, I. Banik and F.F. Becker, Synth. Commun., 30, 3745 (2000); https://doi.org/10.1080/00397910008087002. (b) B.K. Banik, I. Banik, S. Samajdar and M. Wilson, Heterocycles, 63, 283 (2004); https://doi.org/10.3987/COM-03-9914. (c) B.K. Banik, I. Banik and F.F. Becker, Org. Synth., 81, 188 (2005); https://doi.org/10.15227/orgsyn.081.0188.
- (a) F.F. Becker and B.K. Banik, Bioorg. Med. Chem. Lett., 8, 2877 (1998); https://doi.org/10.1016/S0960-894X(98)00520-4. (b) B.K. Banik and F.F. Becker, Curr. Med. Chem., 8, 1513 (2001); https://doi.org/10.2174/0929867013372120. (c) B.K. Banik and F.F. Becker, Bioorg. Med. Chem., 9, 593 (2001); https://doi.org/10.1016/S0968-0896(00)00297-2. (d) F.F. Becker, C. Mukhopadhyay, L. Hackfeld, I. Banik and B.K. Banik, Bioorg. Med. Chem., 8, 2693 (2000); https://doi.org/10.1016/S0968-0896(00)00213-3. (e) B.K. Banik, M.S. Venkatraman, I. Banik and M.K. Basu, Tetrahedron Lett., 45, 4737 (2004); https://doi.org/10.1016/j.tetlet.2004.04.087. (f) K.R. Landis-Piwowar, D. Chen, Q.C. Cui, V. Minic, F.F. Becker, B.K. Banik and Q.P. Dou, Int. J. Mol. Med., 17, 931 (2006); https://doi.org/10.3892/ijmm.17.5.931.(g) B.K. Banik, C. Mukhopadhyay, C.R. Logan and F.F. Becker, Synth. Commun., 37, 3895 (2007); https://doi.org/10.1080/00397910701572209. (h) B.K. Banik, C. Mukhopadhyay and F.F. Becker, Oncol. Lett., 1, 309 (2010); https://doi.org/10.3892/ol_00000055. (i) B.K. Banik and F.F. Becker, Eur. J. Med. Chem., 45, 4687 (2010); https://doi.org/10.1016/j.ejmech.2010.07.033. (j) B.K. Banik, M.K. Basu and F.F. Becker, Oncol. Lett., 1, 1033 (2010); https://doi.org/10.3892/ol.2010.167. (k) J. Short and B.K. Banik, Front. Med. Pharm. Chem., 2, 55 (2014); https://doi.org/10.3389/fchem.2014.00055.
- B.K. Banik, I. Banik, L. Hackfeld and F.F. Becker, Heterocycles, 56, 467 (2001); https://doi.org/10.3987/COM-00-S(K)3.
- B.K. Banik, S. Samajdar and I. Banik, Tetrahedron Lett., 44, 1699 (2003); https://doi.org/10.1016/S0040-4039(02)02823-X.
- B.K. Banik, L. Hackfeld and F.F. Becker, Synth. Commun., 31, 1581 (2001); https://doi.org/10.1081/SCC-100104072.
- (a) B.K. Banik, S. Samajdar, A. Ghatak and F.F. Becker, Heterocycles, 55, 1957 (2001); https://doi.org/10.3987/COM-01-9291. (b) B.K. Banik, Chem.-An Indian J., 1, 149 (2003). (c) S. Samajdar and B.K. Banik, Chem.-An Indian J., 1, 230 (2003); (d) B.K. Banik, I. Banik, N. Aounallah and M. Castillo, Tetrahedron Lett., 46, 7065 (2005); https://doi.org/10.1016/j.tetlet.2005.08.034.
- D. Abrego, D. Banyopadhyay and B.K. Banik, Heterocyclic Lett., 1, 87 (2011).
- (a) B.K. Banik, I. Garcia, F.R. Morales and C. Aguilar, Heterocycl. Commun., 13, 109 (2007); https://doi.org/10.1515/HC.2007.13.2-3.109. (b) B.K. Banik and M. Cardona, Tetrahedron Lett., 47, 7385 (2006); https://doi.org/10.1016/j.tetlet.2006.07.150.
- (a) S. Samajdar, M.K. Basu, F.F. Becker and B.K. Banik, Tetrahedron Lett., 42, 4425 (2001); https://doi.org/10.1016/S0040-4039(01)00752-3. (b) M.K. Basu, S. Samajdar, F.F. Becker and B.K. Banik, Synlett, 319 (2002); https://doi.org/10.1055/s-2002-19774. (c) B.K. Banik, M. Chapa, J. Marquez and M. Cardona, Tetrahedron Lett., 46, 2341 (2005); https://doi.org/10.1016/j.tetlet.2005.01.176. (d) B.K. Banik and R. Garza, Chem. Educ., 12, 75 (2007); (e) I. Banik, S. Samajdar, M.K. Basu and B.K. Banik, Heterocycl. Lett, 1, 111 (2011). (f) N. Srivastava, S.K. Dasgupta and B.K. Banik, Tetrahedron Lett., 44, 1191 (2003); https://doi.org/10.1016/S0040-4039(02)02821-6.
- B.K. Banik, Unpublished Results.
- (a) B.K. Banik, S. Samajdar and I. Banik, J. Org. Chem., 69, 213 (2004); https://doi.org/10.1021/jo035200i. (b) D. Bandyopadhyay, J. Cruz, R.N. Yadav and B.K. Banik, Molecules, 17, 11570 (2012); https://doi.org/10.3390/molecules171011570. (c) D. Bandyopadhyay, G.S. Rivera, I. Salinas, H. Aguilar and B.K. Banik, Molecules, 15, 1082 (2010); https://doi.org/10.3390/molecules15021082. (d) D. Bandyopadhyay, S. Mukherjee and B.K. Banik, Molecules, 15, 2520 (2010); https://doi.org/10.3390/molecules15042520. (e) A. Shaikh and B.K. Banik, Helv. Chim. Acta, 95, 839 (2012); https://doi.org/10.1002/hlca.201100202.
- (a) B.K. Banik, K.J. Barakat, D.R. Wagle, M.S. Manhas and A.K. Bose, J. Org. Chem., 64, 5746 (1999); https://doi.org/10.1021/jo981516s. (b) D. Bandyopadhyay, S. Mukherjee, R. Rodriguez and B.K. Banik, Molecules, 15, 4207 (2010); https://doi.org/10.3390/molecules15064207. (c) D. Bandyopadhyay, J. Cruz and B.K. Banik, Tetrahedron, 68, 10686 (2012); https://doi.org/10.1016/j.tet.2012.06.009. (e) D. Bandyopadhyay, A. Chavez and B.K. Banik, Curr. Med. Chem., (2017); (In press). (f) D. Bandyopadhyay and B.K. Banik,Curr. Med. Chem., (2017); (In press). (g) B.K. Banik, Curr. Med. Chem., (2017); (In press).
- (a) M.K. Basu, F.F. Becker and B.K. Banik, Tetrahedron Lett., 41, 5603 (2000); https://doi.org/10.1016/S0040-4039(00)00917-5. (b) M.K. Basu, F.F. Becker and B.K. Banik, J. Chem. Res., 406 (2000); https://doi.org/10.3184/030823400103167877. (c) D. Bandyopadhyay, S. Mukherjee, L. Turrubiartes and B.K. Banik, Ultrason. Sonochem., 19, 969 (2012); https://doi.org/10.1016/j.ultsonch.2011.11.009.
- D. Bandyopadhyay, Green Synthetic Approaches for Biologically Relevant Heterocycles, Elsevier, pp. 517-552 (2014).
- (a) B.K. Banik, Heterocycl. Lett., 4, 441 (2014); (b) B.K. Banik, Heterocycl. Lett., 4, 453 (2014); (c) B.K. Banik, Heterocycl. Lett., 4, 463 (2014); (d) B.K. Banik, Heterocycl. Lett., 4, 467 (2014); (e) B.K. Banik, Asian J. Org. Med. Chem., 1, 1 (2016); https://doi.org/10.14233/ajomc.2016.AJMOC-EIC.
References
(a) B.K. Banik, A. Ghatak and F.F. Becker, J. Chem. Soc., Perkin Trans. 1, 2179 (2000); https://doi.org/10.1039/b002833i. (b) A. Ghatak, F.F. Becker and B.K. Banik, Heterocycles, 53, 2769 (2000); https://doi.org/10.3987/COM-00-9019. (c) S. Chandra, R.N. Yadav, L. Lareeb and B.K. Banik, Chem. Educ., 20,4 (2015).
A. Ghatak and B.K. Banik, Heterocycl. Lett., 1, 99 (2011).
(a) B.K. Banik, Heterocyclic Scaffolds I, Topics in Heterocyclic Chemistry, Springer, vol. 22, pp. 1-379 (2010). (b) B.K. Banik, β-Lactams: Synthesis and Biological Evaluation, Topics in Heterocyclic Chemistry, Springer, vol. 30, pp. 1-226 (2012). (c) B.K. Banik, Tetrahedron, 68, 10627 (2012); https://doi.org/10.1016/S0040-4020(12)01701-2. (d) I. Banik and B.K. Banik, Microwave-Induced Chemical Manipulation of β-Lactam, Topics in Heterocyclic Chemistry, Springer, vol. 88, pp. 781-1007 (2012). (e) B.K. Banik, Beta Lactams: Novel Synthetic Pathways and Applications, Springer, pp. 1-419 (2017). (f) P.T. Parvatkar, P.S. Parameswaran and B.K. Banik, ed.: B.K. Banik Solid Phase Synthesis of β-Lactams: Results and Scope; In: Beta Lactams: Novel Synthetic Pathways and Applications, Ed. Spinger, pp. 253-284 (2017). (g) S. Basu and B.K. Banik, ed.: B.K. Banik, Beta Lactams as Clinically Active Molecules, In: Beta Lactams: Novel Synthetic Pathways and Applications, Springer, pp. 285-310 (2017). (h) B.K. Banik, Synthesis and Biological Studies of Novel β-Lactams, CRC Book, pp. 31-72 (2013).
(a) B.K. Banik, S. Samajdar, I. Banik, O. Zegrocka and F.F. Becker, Heterocycles, 55, 227 (2001); https://doi.org/10.3987/COM-00-9100. (b) I. Banik, S. Samajdar and B.K. Banik, Heterocycl. Lett., 1, 47 (2011).
S. Samajdar, I. Banik and B.K. Banik, Heterocycl. Lett., 1, 41 (2011).
B.K. Banik, S. Samajdar and F.F. Becker, Mol. Med. Rep., 3, 319 (2010); https://doi.org/10.3892/mmr_00000259.
(a) I. Banik, F.F. Becker and B.K. Banik, J. Med. Chem., 46, 12 (2003); https://doi.org/10.1021/jm0255825. (b) B.K. Banik, I. Banik and L. Hackfeld, Heterocycles, 59, 505 (2003); https://doi.org/10.3987/COM-02-S76. (c) B.K. Banik, F.F. Becker and I. Banik, Bioorg. Med. Chem., 12, 2523 (2004); https://doi.org/10.1016/j.bmc.2004.03.033. (d) B.K. Banik, Curr. Med. Chem., 11, 1 (2012); https://doi.org/10.2174/0929867043364892. (e) B.K. Banik, I. Banik and F.F. Becker, Bioorg. Med. Chem., 13, 3611 (2005); https://doi.org/10.1016/j.bmc.2005.03.044. (f) B.K. Banik and F.F. Becker, Mol. Med. Rep., 3, 315 (2010); https://doi.org/10.3892/mmr_00000257. (g) B.K. Banik, I. Banik and F.F. Becker, Eur. J. Med. Chem., 45, 846 (2010); https://doi.org/10.1016/j.ejmech.2009.11.024. (h) B.K. Banik, Int. Innov., 50 (2011). (i) B.K. Banik, Int. Innov., 114 (2012).
(a) B.K. Banik, M.S. Manhas and A.K. Bose, Tetrahedron Lett., 38, 5077 (1997); https://doi.org/10.1016/S0040-4039(97)01130-1. (b) B.K. Banik, O. Zegrocka, M.S. Manhas and A.K. Bose, Heterocycles, 46, 173 (1997); https://doi.org/10.3987/COM-97-S66. (c) B.K. Banik, M.S. Manhas and A.K. Bose, J. Org. Chem., 59, 4714 (1994); https://doi.org/10.1021/jo00096a004. (d) B.K. Banik, O. Zegrocka, M.S. Manhas and A.K. Bose, Heterocycles, 78, 2443 (2009); https://doi.org/10.3987/COM-09-11729. (e) B.K. Banik and M.S. Manhas, Tetrahedron, 68, 10769 (2012); https://doi.org/10.1016/j.tet.2012.01.078.
(a) B.K. Banik, M. Suhendra, I. Banik and F.F. Becker, Synth. Commun., 30, 3745 (2000); https://doi.org/10.1080/00397910008087002. (b) B.K. Banik, I. Banik, S. Samajdar and M. Wilson, Heterocycles, 63, 283 (2004); https://doi.org/10.3987/COM-03-9914. (c) B.K. Banik, I. Banik and F.F. Becker, Org. Synth., 81, 188 (2005); https://doi.org/10.15227/orgsyn.081.0188.
(a) F.F. Becker and B.K. Banik, Bioorg. Med. Chem. Lett., 8, 2877 (1998); https://doi.org/10.1016/S0960-894X(98)00520-4. (b) B.K. Banik and F.F. Becker, Curr. Med. Chem., 8, 1513 (2001); https://doi.org/10.2174/0929867013372120. (c) B.K. Banik and F.F. Becker, Bioorg. Med. Chem., 9, 593 (2001); https://doi.org/10.1016/S0968-0896(00)00297-2. (d) F.F. Becker, C. Mukhopadhyay, L. Hackfeld, I. Banik and B.K. Banik, Bioorg. Med. Chem., 8, 2693 (2000); https://doi.org/10.1016/S0968-0896(00)00213-3. (e) B.K. Banik, M.S. Venkatraman, I. Banik and M.K. Basu, Tetrahedron Lett., 45, 4737 (2004); https://doi.org/10.1016/j.tetlet.2004.04.087. (f) K.R. Landis-Piwowar, D. Chen, Q.C. Cui, V. Minic, F.F. Becker, B.K. Banik and Q.P. Dou, Int. J. Mol. Med., 17, 931 (2006); https://doi.org/10.3892/ijmm.17.5.931.(g) B.K. Banik, C. Mukhopadhyay, C.R. Logan and F.F. Becker, Synth. Commun., 37, 3895 (2007); https://doi.org/10.1080/00397910701572209. (h) B.K. Banik, C. Mukhopadhyay and F.F. Becker, Oncol. Lett., 1, 309 (2010); https://doi.org/10.3892/ol_00000055. (i) B.K. Banik and F.F. Becker, Eur. J. Med. Chem., 45, 4687 (2010); https://doi.org/10.1016/j.ejmech.2010.07.033. (j) B.K. Banik, M.K. Basu and F.F. Becker, Oncol. Lett., 1, 1033 (2010); https://doi.org/10.3892/ol.2010.167. (k) J. Short and B.K. Banik, Front. Med. Pharm. Chem., 2, 55 (2014); https://doi.org/10.3389/fchem.2014.00055.
B.K. Banik, I. Banik, L. Hackfeld and F.F. Becker, Heterocycles, 56, 467 (2001); https://doi.org/10.3987/COM-00-S(K)3.
B.K. Banik, S. Samajdar and I. Banik, Tetrahedron Lett., 44, 1699 (2003); https://doi.org/10.1016/S0040-4039(02)02823-X.
B.K. Banik, L. Hackfeld and F.F. Becker, Synth. Commun., 31, 1581 (2001); https://doi.org/10.1081/SCC-100104072.
(a) B.K. Banik, S. Samajdar, A. Ghatak and F.F. Becker, Heterocycles, 55, 1957 (2001); https://doi.org/10.3987/COM-01-9291. (b) B.K. Banik, Chem.-An Indian J., 1, 149 (2003). (c) S. Samajdar and B.K. Banik, Chem.-An Indian J., 1, 230 (2003); (d) B.K. Banik, I. Banik, N. Aounallah and M. Castillo, Tetrahedron Lett., 46, 7065 (2005); https://doi.org/10.1016/j.tetlet.2005.08.034.
D. Abrego, D. Banyopadhyay and B.K. Banik, Heterocyclic Lett., 1, 87 (2011).
(a) B.K. Banik, I. Garcia, F.R. Morales and C. Aguilar, Heterocycl. Commun., 13, 109 (2007); https://doi.org/10.1515/HC.2007.13.2-3.109. (b) B.K. Banik and M. Cardona, Tetrahedron Lett., 47, 7385 (2006); https://doi.org/10.1016/j.tetlet.2006.07.150.
(a) S. Samajdar, M.K. Basu, F.F. Becker and B.K. Banik, Tetrahedron Lett., 42, 4425 (2001); https://doi.org/10.1016/S0040-4039(01)00752-3. (b) M.K. Basu, S. Samajdar, F.F. Becker and B.K. Banik, Synlett, 319 (2002); https://doi.org/10.1055/s-2002-19774. (c) B.K. Banik, M. Chapa, J. Marquez and M. Cardona, Tetrahedron Lett., 46, 2341 (2005); https://doi.org/10.1016/j.tetlet.2005.01.176. (d) B.K. Banik and R. Garza, Chem. Educ., 12, 75 (2007); (e) I. Banik, S. Samajdar, M.K. Basu and B.K. Banik, Heterocycl. Lett, 1, 111 (2011). (f) N. Srivastava, S.K. Dasgupta and B.K. Banik, Tetrahedron Lett., 44, 1191 (2003); https://doi.org/10.1016/S0040-4039(02)02821-6.
B.K. Banik, Unpublished Results.
(a) B.K. Banik, S. Samajdar and I. Banik, J. Org. Chem., 69, 213 (2004); https://doi.org/10.1021/jo035200i. (b) D. Bandyopadhyay, J. Cruz, R.N. Yadav and B.K. Banik, Molecules, 17, 11570 (2012); https://doi.org/10.3390/molecules171011570. (c) D. Bandyopadhyay, G.S. Rivera, I. Salinas, H. Aguilar and B.K. Banik, Molecules, 15, 1082 (2010); https://doi.org/10.3390/molecules15021082. (d) D. Bandyopadhyay, S. Mukherjee and B.K. Banik, Molecules, 15, 2520 (2010); https://doi.org/10.3390/molecules15042520. (e) A. Shaikh and B.K. Banik, Helv. Chim. Acta, 95, 839 (2012); https://doi.org/10.1002/hlca.201100202.
(a) B.K. Banik, K.J. Barakat, D.R. Wagle, M.S. Manhas and A.K. Bose, J. Org. Chem., 64, 5746 (1999); https://doi.org/10.1021/jo981516s. (b) D. Bandyopadhyay, S. Mukherjee, R. Rodriguez and B.K. Banik, Molecules, 15, 4207 (2010); https://doi.org/10.3390/molecules15064207. (c) D. Bandyopadhyay, J. Cruz and B.K. Banik, Tetrahedron, 68, 10686 (2012); https://doi.org/10.1016/j.tet.2012.06.009. (e) D. Bandyopadhyay, A. Chavez and B.K. Banik, Curr. Med. Chem., (2017); (In press). (f) D. Bandyopadhyay and B.K. Banik,Curr. Med. Chem., (2017); (In press). (g) B.K. Banik, Curr. Med. Chem., (2017); (In press).
(a) M.K. Basu, F.F. Becker and B.K. Banik, Tetrahedron Lett., 41, 5603 (2000); https://doi.org/10.1016/S0040-4039(00)00917-5. (b) M.K. Basu, F.F. Becker and B.K. Banik, J. Chem. Res., 406 (2000); https://doi.org/10.3184/030823400103167877. (c) D. Bandyopadhyay, S. Mukherjee, L. Turrubiartes and B.K. Banik, Ultrason. Sonochem., 19, 969 (2012); https://doi.org/10.1016/j.ultsonch.2011.11.009.
D. Bandyopadhyay, Green Synthetic Approaches for Biologically Relevant Heterocycles, Elsevier, pp. 517-552 (2014).
(a) B.K. Banik, Heterocycl. Lett., 4, 441 (2014); (b) B.K. Banik, Heterocycl. Lett., 4, 453 (2014); (c) B.K. Banik, Heterocycl. Lett., 4, 463 (2014); (d) B.K. Banik, Heterocycl. Lett., 4, 467 (2014); (e) B.K. Banik, Asian J. Org. Med. Chem., 1, 1 (2016); https://doi.org/10.14233/ajomc.2016.AJMOC-EIC.