Spotlight: Supramolecular catalysis
محورهای موضوعی : Iranian Journal of Catalysis
1 - Faculty of Chemistry, Bu-Ali Sina University, Hamedan 6517838683, Iran
کلید واژه: Supramolecular catalysis, Noncovalent intermolecular forces,
چکیده مقاله :
Morteza Torabi was born in 1995 in Hamedan, Iran. He received his B.Sc. in Applied Chemistry (2017) and M.Sc. in Organic Chemistry (2019) from Bu-Ali Sina University under the supervision of Professor Mohammad Ali Zolfigol. He is currently working towards his Ph.D. under the supervision of Professor Mohammad Ali Zolfigol at Bu-Ali Sina University. His research interest is the design, synthesis and characterization of acidic magnetic nanoparticles, magnetic ionic liquids, and urea based compound as catalysts and their applications in organic synthesis.
[1] J. M. Lehn, Chem. Soc. Rev., 36 (2007) 151-160.
[2] I. V. Kolesnichenko, E. V. Anslyn, Chem. Soc. Rev., 46 (2017) 2385-2390.
[3] B. A. Moyer, J. F. Birdwell, P. V. Bonnesen, L. H. Delmau, K.Gloe, (2005). Macrocyclic Chemistry: Current Trends and Future Perspectives. Netherlands: Springer.
[4] B. Wang, E. V. Anslyn, (2011). Chemosensors: principles, strategies, and applications (Vol. 15). John Wiley & Sons.
[5] a) M. Ikeda, Bull. Chem. Soc. Jpn., 86 (2013) 10-24; b) A. Priimagi, G. Cavallo, P. Metrangolo, G. Resnati, Acc. Chem. Res., 46 (2013) 2686- 2695.
[6] S. Erbas-Cakmak, D. A. Leigh, C. T. McTernan, A. L. Nussbaumer, Chem. Rev., 115 (2015) 10081-10206.
[7] Q. Q. Wang, Handbook of Macrocyclic Supramolecular Assembly, (2020) 829-875.
[8] D. Kauerhof, J. Niemeyer, ChemPlusChem, 85 (2020) 889-899.
[9] M. Mastalerz, Acc. Chem. Res., 51(2018) 2411-2422.
[10] E. Alvira, C. Cativiela, J. García, J. Mayoral, Tetrahed. Lett., 36 (1995) 2129-2132.
[11] S. P. Kim, A. G. Leach, K. N. Houk, J. Org. Chem., 67 (2002) 4250-4260.
[12] V. Luzhkov, J. Åqvist, Chem. Phys. Lett., 302 (1999) 267-272.
[13] G. Hattori, T. Hori, Y. Miyake and Y. Nishibayashi, J. Am. Chem. Soc., 129 (2007) 12930-12931.
[14] Y. Li, Y. Feng, Y. M. He, F. Chen, J. Pan, Q. H. Fan, Tetrahedron. Lett., 49 (2008) 2878-2881.
[15] Y. Suzaki, K. Shimada, E. Chihara, T. Saito, Y. Tsuchido, K. Osakada, Org. Lett., 13 (2011) 3774-3777.
[16] Q. Q. Wang, (2020). Handbook of Macrocyclic Supramolecular Assembly, 829-875.
[17] Y. Fang, J. A. Powell, E. Li, Q. Wang, Z. Perry, A. Kirchon, X. Yang, Z. Xiao, C. Zho, L. Zhang, F. Huang, H. C. Zhou, Chem. Soc. Rev., 48 (2019) 4707-4730.
[18] T. Hasell, A. I. Cooper, Nat. Rev. Mater., 1 (2016) 11-14.
[19] A. Pappalardo, R. Puglisi, G. Trusso Sfrazzetto, Catalysts, 9 (2019) 630-651.
[20] Y. Voloshin, I. Belaya, R. Krämer, In The Encapsulation Phenomenon. Springer, Cham (2016) 499-523.
[21] P. Sarkar, S. Sarkar, P. Ghosh, Beilstein J. Org. Chem., 15 (2019) 1505-1514.
[22] M. Yoshizawa, M. Tamura, M. Fujita, Science, 312 (2006) 251-254.
[23] Y. A. Tayade, S. A. Padvi, Y. B. Wagh, D. S. Dalal, Tetrahedron Lett., 56 (2015) 2441-2447.
[24] D. Kauerhof, J. Niemeyer, ChemPlusChem, 85 (2020) 889-899.
[25] J. Simões, Â. de Fátima, A. Sabino, F. Aquino, D. Leite, L. C. Barbosa, S. Fernandes, Org. Biomol. Chem., 29 (2013) 5069-5073.
[26] C. Gaeta, C. Talotta, M. De Rosa, P. La Manna, A. Soriente, P. Neri, Chem. Eur., 25 (2019) 4899-4913.
[27] L. Catti, K. Tiefenbacher, Chem Commun, 51 (2015) 892-894.
[28] Z. Shu, Y. Chen, H. Yu, X. Liao, C. Liu, H. Tang, S. Li, P. Yang, Chem Commun, 55 (2019) 5491-5494.
[29] C. J. Walter, H. L. Anderson, J. K. Sanders, J Chem Soc Chem Comm, 5 (1993) 458-460.
[30] O. Sahin, S. Eymur, A. Uyanik, E. Akceylan, M. Yilmaz, Polycycl. Aromat. Comp., 38 (2018) 168-179.
[31] J. Chen, J. Rebek, Org. Lett., 4 (2002) 327-329.
[32] S. R. Shenoy, F. R. Pinacho Crisóstomo, T. Iwasawa, J. Rebek, J. Am. Chem. Soc., 7 (2008) 0763-0763.