Aryl diazonium nanomagnetic sulfate and potassium iodide: An iodination process

Tetrahedron Letters

Volumn 55, Issue 27, 2014, Pages 3648-3651

  Kolvari, Eskandar ^a   Amoozadeh, Ali ^a   Koukabi, Nadiya ^a   Otokesh, Somayeh ^a   Isari, Mohsen ^a  

^a SEMNAN UNIVERSITY   (Iran)

Author keywords

Aryl diazonium nanomagnetic sulfate; Aryl iodide; Iodination; Solvent free condition

Indexed keywords

AROMATIC AMINE; ARYLDIAZONIUM NANOMAGNETIC SULFATE; DIAZONIUM COMPOUND; POTASSIUM IODIDE; SODIUM NITRITE; SOLVENT; SULFATE; UNCLASSIFIED DRUG; IODIDE; MAGNETIC NANOPARTICLE;

ARTICLE; CHEMICAL STRUCTURE; DIAZOTIZATION; IODINATION; SYNTHESIS; TEMPERATURE; ARYLATION; COLUMN CHROMATOGRAPHY; CRYSTALLIZATION; REACTION TIME;

EID: 84902213190     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2014.02.073     Document Type: Article

References (22)

1. A.B. Naidu, and G. Sekar Synthesis 2010 579 586
2. T. Pacuszka, and M. Panasiewicz J. Labelled Compd. Radiopharm. 43 2000 1255 1263
3. D.L. Comins, M.F. Baevsky, and H. Hong J. Am. Chem. Soc. 114 1992 10971 10972
4. D.M. Springer, B.-Y. Luh, J. Goodrich, and J.J. Bronson Bioorg. Med. Chem. 11 2003 265 279
5. V.H. Rawal, C. Michoud, and R. Monestel J. Am. Chem. Soc. 115 1993 3030 3031
6. C.Y. Hong, and L.E. Overman Tetrahedron Lett. 35 1994 3453 3456
7. K.C. Nicolaou, J. Xu, F. Murphy, S. Barluenga, O. Baudoin, H.-X. Wei, D.L.F. Gray, and T. Ohshima Angew. Chem., Int. Ed. 38 1999 2447 2451
8. A. Endo, A. Yanagisawa, M. Abe, S. Tohma, T. Kan, and T. Fukuyama J. Am. Chem. Soc. 124 2002 6552 6554
9. J.H. Chang, H.-U. Kang, I.-H. Jung, and C.-G. Cho Org. Lett. 12 2010 2016 2018
10. T. Sandmeyer Ber. Dtsch. Chem. Ges. 17 1884 1633 1635
11. F. Nemati, and A. Elhampour Sci. Iranica 19 2012 1594 1596
12. V.D. Filimonov, N.I. Semenischeva, E.A. Krasnokutskaya, A.N. Tretyakov, H.Y. Hwang, and K.-W. Chi Synthesis 2008 185 187
13. A. Zarei, A.R. Hajipour, and L. Khazdooz Synthesis 2009 941 944
14. D.A. Gorlushko, V.D. Filimonov, E.A. Krasnokutskaya, N.I. Semenischeva, B.S. Go, H.Y. Hwang, E.H. Cha, and K.-W. Chi Tetrahedron Lett. 49 2008 1080 1082
15. A.R. Hajipour, M. Arbabian, and A.E. Ruoho J. Org. Chem. 67 2002 8622 8624
16. G.A. Olah, Q. Wang, G. Sandford, and G.K. Surya Prakash J. Org. Chem. 58 1993 3194 3195
17. S. Agarwal, U. Aware, A. Patil, V. Rohera, M. Ghate, M. Jain, and P. Patel Bull. Korean Chem. Soc. 33 2012 377 378
18. R. Johnsson, A. Meijer, and U. Ellervik Tetrahedron 61 2005 11657 11663
19. H. Zolinger Azo and Diazo Chemistry, Aliphatic and Aromatic Compounds 1961 Interscience Publishers London
20. N. Koukabi, E. Kolvari, M.A. Zolfigol, A. Khazaei, B.S. Shaghasemi, and B. Fasahati Adv. Synth. Catal. 354 2012 2001 2008
21. E.A. Krasnokutskaya, N.I. Semenischeva, V.D. Filimonov, and P. Knochel Synthesis 2007 81 84
22. A. Zarei, A.R. Hajipour, L. Khazdooz, B.F. Mirjalili, and A. Najafi Chermahini Dyes Pigm. 81 2009 240 244