Spotlight: Use of 1,3-dioxan-5-one derivatives in organic synthesis
محورهای موضوعی : Iranian Journal of Catalysis
Mohammad Javad Poursharifi
1
(Department of Chemistry, Science and Research Branch, Islamic Azad University, Tehran 1477893855, Iran.)
کلید واژه: Mannich reaction, Diels-Alder cycloaddition, Baylis-Hillman reaction, Claisen-Schmidt condensation, Dihydroxyacetone, 1, 3-Dioxan-5-one,
چکیده مقاله :
Mohammad Javad Poursharifi was born in 1971 in Ray City, Iran. He obtained his B.Sc. (1994) from Kharazmi University, Tehran. He then completed his M.Sc. studies in Organic Chemistry (2008) from Islamic Azad University, Saveh Branch, Iran. Currently, he is working towards his Ph.D. under the supervision of Professor Mohammad Majid Mojtahedi and Professor Mahmood M. Hashemi at Islamic Azad University, Science and Research Branch. His research involves synthetic applications of 1,3-dioxan-5-one derivatives.
[1] A.R. Massah, R.J. Kalbasi, M. Toghyani, Iran. J. Catal. 2 (2012) 41-49.
[2] R. Thayumanavan, B. Dhevalapally, K. Sakthivel, F. Tanaka, C.F. Barbas, III, Tetrahedron Lett. 43 (2002) 3817-3820.
[3] D. Basavaiah, G. Veeraraghavaiah, Chem. Soc. Rev. 41 (2012) 68-78.
[4] A. Dhakshinamoorthy, M. Alvaro, H, Garcia, Adv. Synth. Catal. 352 (2010) 711-717.
[5] D. Enders, M. Voith, A. Lenzen, Angew. Chem. Int. Ed. 44 (2005) 1304-1325.
[6] D. Enders, S. Breukers, L.F. Reichenbach, Encyclopedia of Reagents for Organic Synthesis, John Wiley & Sons, 2001.
[7] C. Grondal, D. Enders, Adv. Synth. Catal. 349 (2007) 694-702.
[8] N. Palyam, M. Majewski, J. Org. Chem. 74 (2009) 4390-4392.
[9] M. Yasuda, Y. Saga, T. Tokunaga, S. Itoh, S. Aoki, Tetrahedron 75 (2019) 757-777.
[10] M.J. Poursharifi, M.M. Mojtahedi, M.S. Abaee, M.M. Hashemi, Heterocyclic Commun. 25 (2019) 85-90.
[11] J.M. Trajkovic, Z. Ferjancic, R.N. Saicic, Tetrahedron 73 (2017) 2629-2632.
[12] M.M. Mojtahedi, M. Mehraban, K. Darvishi, M.S. Abaee, Heterocyclic Commun. 23 (2017) 91-95.
[13] M.M. Mojtahedi, K. Darvishi, M.S. Abaee, M.R. Halvagar, Can. J. Chem. 95 (2017) 785-791.
[14] J. Marjanovic Trajkovic, V. Milanovic, Z. Ferjancic, R.N. Saicic, Eur. J. Org. Chem. (2017) 6146-6153.
[15] D. Sánchez, H. Carneros, A. Castro-Alvarez, E. Llàcer, F. Planas, J. Vilarrasa, Tetrahedron Lett. 57 (2016) 5254-5258.
[16] H. Lago-Santomé, R. Meana-Pañeda, R. Alonso, J. Org. Chem. 79 (2014) 4300-4305.
[17] D. Sánchez, D. Bastida, J. Burés, C. Isart, O. Pineda, J. Vilarrasa, Org. Lett. 14 (2012) 536-539.
[18] H. Zhang, S.S.V. Ramasastry, F. Tanaka, C.F. Barbas III, Adv. Synth. Catal 350 (2008) 791-796.
[19] M.S. Abaee, M.M. Mojtahedi, V. Hamidi, A.W. Mesbah, W. Massa, Synthesis 40 (2008) 2122-2126.
[20] R.A. Aungst Jr, R.L. Funk, Org. Lett. 3 (2001) 3553-3555.
[21] Y. Yoshimura, K. Asami, H. Matsui, H. Tanaka, H. Takahata, Org. Lett. 8 (2006) 6015-6018.
