Spotlight- Trityl Chloride: As a multi propose reagent
محورهای موضوعی : Iranian Journal of Catalysis
Mahmoud Zarei
1
(Faculty of Chemistry, Bu-Ali Sina University, Hamedan 6517838683, Iran)
کلید واژه:
چکیده مقاله :
Mahmoud Zarei was born in Hamedan, Iran in1986. He received his B.Sc. in Pure Chemistry (2010) from Islamic Azad University Arak and M.Sc. in Organic Chemistry (2013) at Bu-Ali Sina University, Iran. He is currently working towards his Ph.D. under the supervision of Professor Mohammad Ali Zolfigol. His research interest is catalysis, including the application of homogeneous and heterogeneous catalysis in organic synthesis.
[1] (a) F. Crestey, L.K. Ottesen, J.W. Jaroszewski, H. Franzyk, Tetrahedron Lett. 49 (2008) 5890–5893. (b) S.D. Wiedner, E. Vedejs, J. Org. Chem. 77 (2012) 1045−1055. (c) D.A. Straus, C. Zhang, T.D. Tilley, J. Organometal. Chem. 369 (1989) 13-l7. (d) Z. Gholamzadeh, M.R. Naimi-Jamal, A. Maleki, C.R. Chim. 17 (2014) 994–1001. (e) R.L. Harding, T.D.H. Bugg, Tetrahedron Lett. 41 (2000) 2729–2731. (f) K.C. Schreiber, V.P. Fernandez, J. Org. Chem. 26 (1961) 2478−2479. (g) I.N. Redwan, M. Grøtli, J. Org. Chem. 77 (2012) 7071−7075.
[2] T.W. Green, P.G.M. Wuts, Protective Group in Organic Synthesis, 3rd ed., John Wiley and Sons, New York, 1999.
[3] T. Mukaiyama, S. Kobayashi, J. Organomet. Chem. 382 (1990) 39–52.
[4] W.E. Bachmann, C.R. Hauser, B.E. Hudson Jr., Org. Synth. 3 (1955) 841.
[5] (a) Z. Dominguez, H. Dang, M.J. Strouse, M.A. Garcia-Garibay, J. Am. Chem. Soc. 124 (2002) 7719-7727. (b) R.E. Oyler, B.E. Ketz, T.E. Glass, Tetrahedron Lett. 41 (2000) 8247–8250.
[6] V. Kotek, N. Chudıkova, T. Tobrman, D. Dvorak, Org. Lett. 12 (2010) 5724-5727.
[7] (a) A. Khazaei, M.A. Zolfigol, A.R. Moosavi-Zare, F. Abi, A. Zare, H. Kaveh, V Khakyzadeh, M. Kazem-Rostami, A. Parhami, Tetrahedron 69 (2013) 212-218. (b) A. Khazaei, M.A. Zolfigol, A.R. Moosavi-Zare, A. Zare, A. Parhami, A. Khalafi-Nezhad, Appl. Catal. A 386 (2010) 179–187. (c) A. Khazaei, M.A. Zolfigol, A.R. Moosavi-Zare, A. Zare, M. Khojasteh, Z. Asgari, V. Khakyzadeh, A. Khalafi-Nezhad, Catal. Commun. 20 (2012) 54–57. (d) A. Zare, M. Merajoddin, A. Hasaninejad, A.R. Moosavi-Zare, V. Khakyzadeh, C.R. Chim. 16 (2013) 380–384. (e) A. Zare, M. Merajoddin, A.R. Moosavi‐Zare, M. Zarei, Chin. J. Catal. 35 (2014) 85–89.
[8] L. Zou, H.L. Pang, PH Chan, Z.S. Huang, L.Q. Gu, K.Y. Wong. Carbohydr. Res. 343 (2008) 2932–
2938.
[9] (a) J.T. Lundquist, A.D. Satterfield, J.C. Pelletier, Org. Lett. 8(2006) 3915-3918. (b) R. Bernini, M. Maltese, Tetrahedron Lett. 51 (2010) 4113–4116.
[10] M.B.D. Andaloussi, F. Mohr, J. Organometal. Chem. 695 (2010) 1276–1280.
[11] J.C. Kaila, A.B. Baraiya, A.N. Pandya, H.B. Jalani, K.K. Vasu, V. Sudarsanam, Tetrahedron Lett. 50 (2009) 3955–3958.
