Nano-cellulose-OSnCl4-x: Green and natural-based renewable nanocatalyst for one-pot synthesis of 2-amino-3-phenylsulfonyl-4H-pyran derivatives
Subject Areas : Iranian Journal of Catalysis
Sayed Rasul Shafe-Mehrabadi
1
(Department of Chemistry, Yazd Branch, Islamic Azad University, Yazd, Iran)
Bahareh Sadeghi
2
(Department of Chemistry, Central Tehran Branch, Islamic Azad University, Tehran, Iran)
Mohammad Hossein Mosslemin
3
(Department of Chemistry, Yazd Branch, Islamic Azad University, Yazd, Iran)
Saeedeh Hashemian
4
(Department of Chemistry, Yazd Branch, Islamic Azad University, Yazd, Iran)
Keywords:
Abstract :
[1] R. S. Bon, B. Van Vliet, N. E. Sprenkels, R. F. Schmitz, F. J. J. de Kanter, C. V. Stevens, M. Swart, F. Matthias Bickelhaupt, M. B. Groen, R. V. A. Orru, J. Org. Chem. 70 (2005) 3542-3553.
[2] J. Zhu, H. Bienayme, “Multicomponent Reactions” Germany-Weinheim: Wiley‐VCH Verlag GmbH & Co. KgaA, 2005.
[3] A. Dömling, Chem. Rev. 106 (2006) 17-89.
[4] R. W. Armstrong, A. P. Combs, P. A. Tempest, S. D. Brown, T. A. Keating, Acc. Chem. Res. 29 (1996) 123-131.
[5] N. K. Terret, M. Gardner, D. W. Gordon, R. J. Kobylecki, J. Steel, Tetrahedron 51(1995) 8135-8173.
[6] J. Kaur, D. Utreja, E. Malhora, N. Jain, Sh. Sharma, Curr. Org. Chem. 16 (2019) 17-37.
[7] S. Rostamnia, RSC Adv. 5 (2015) 97044-97065.
[8] S. J. Mohr, M. A. Chirigos, F. S. Fuhrman, J. W. Pryor, Cancer Res. 35 (1975) 3750-3754.
[9] A. M. El-Agrody, M. S. Abd El-Latif, N. A. El-Hady, A. H. Fakery, A. H. Bedair, Molecules 6 (2001) 519-257.
[10] A. H. Bedair, N. A. El-Hady, M. S. Abd El-Latif, A. H. Fakery, A. M. El-Agrody, Il Farmaco 55 (2000) 708-717.
[11] A. M. El-Agrody, M. H. El-Hakim, M. S. Abd El-Latif, A. H. Fakery, E. S. M. El-Sayed, K. A. El-Ghareab, Acta Pharm. 50 (2000) 111-120.
[12] A. Martinez-Grau, J. L. Marco, Bioorg. Med. Chem. Lett. 7 (1997) 3165-3170.
[13] C. Medina, M. J. Santos-Martinez, A. Radomski, O. I. Corrigan, M. W. Radomski, Br. J. Pharmacol. 150 (2007) 552-558.
[14] S. Dehghanpoor, B. Sadeghi, M. H. Mosslemin, Russ. J. Org. Chem. 55 (2019) 1957-1960.
[15] B. Sadeghi, M. Bouslik, M. R. Shishehbore, J. Iran. Chem. Soc. 12 (2015) 1801-1808.
[16] A. Dehghani Ashkzari, B. Sadeghi, S. Zavar, Polycycl. Aromat. Compound. 40 (2020) 954-959.
[17] B. Sadeghi, Res. Chem. Intermed. 45 (2019) 4897-4906.
[18] E. Abyar, B. Sadeghi, M. H. Mosslemin, Polycycl. Aromat. Compound. 41 (2021) 920-928.
[19] F. Manouchehri, B. Sadeghi, F. Najafi, M. H. Mosslemin, J. Iran. Chem. Soc. 15 (2018) 1673-1683.
[20] S. R. Shafe-Mehrabadi, B. Sadeghi, M. H. Mosslemin, S. Hashemian, J. Iran. Chem. Soc. 18 (2021) 1137-1145.
[21] M. Kamali-Gharamaleki, B. Sadeghi, M. Rouhani, Z. Mirjafary, React. Kinet. Mech. Catal. 132 (2021) 251-260.
[22] B. F. Mirjalili, A. Bamoniri, S. Nazemian, R. Zare Reshquiyea, J. Nanostruct. 9(1) (2019) 183-189.
[23] J. Safaei-Ghomi, R. Teymuri, H. Shahbazi-Alavi, A. Ziarati, Chin. Chem. Lett. 24 (2013) 921-925.
[24] M. Ding, L. Zhang, H. Guo, M. Zhong, J. Chem. Res. 37 (2013) 780-782.
[25] S.-S. Jin, H. Wang, H.-Y. Guo, Tetrahedron Lett. 54 (2013) 2353-2356.
[26] Y-R. Zhang, J-T. Chen, B. Hao, R. Wang, P-C Ma, Carbohydr. Polym. 240 (2020) 116318.
[27] S. Maiti, J. Jayaramudu, K. Das, S.M. Reddy, R. Sadiku, S.S. Ray, D. liu, Carbohydr. Polym. 98 (2013) 562-567.