1
Department of hemistry, Faculty of Science, Urumia University, Pstcode 57154, Urumia, I.R. IRAN
2
Departent of Chemistry, Manchester University, Manchester, M13 9PL, ENGLAND
10.30492/ijcce.1996.10131
Abstract
Treatment of 10-bromoanthralin (1) with several thiophenols (2) gave the corresponding 10-arylthioanthralins (3) in high yields. Oxidation of thioanthralins (3a-c) and (3k-m) using an excess of m-chloroperbenzoic acid gave the corresponding sulfones (4a-c) and (4k-m) in good yields. Oxidation of thioanthralins (3d-f) gave a mixture of the corresponding sulfones (4d-f) and anthralin-10,10'-dehydrodimer (5). Oxidation of thioanthralins (3g-j) afforded only anthralin-10,10'-dehydrodimer (5) with no evidence of sulfone.
Khalafy, J., & Pruce, J. M. (1996). Synthesis of New 10-Arylthioanthralins and Oxidation of Thioanthralins to Their Corresponding Sulfones. Iranian Journal of Chemistry and Chemical Engineering, 15(1), 1-7. doi: 10.30492/ijcce.1996.10131
MLA
Jabbar Khalafy; John Malcolm Pruce. "Synthesis of New 10-Arylthioanthralins and Oxidation of Thioanthralins to Their Corresponding Sulfones". Iranian Journal of Chemistry and Chemical Engineering, 15, 1, 1996, 1-7. doi: 10.30492/ijcce.1996.10131
HARVARD
Khalafy, J., Pruce, J. M. (1996). 'Synthesis of New 10-Arylthioanthralins and Oxidation of Thioanthralins to Their Corresponding Sulfones', Iranian Journal of Chemistry and Chemical Engineering, 15(1), pp. 1-7. doi: 10.30492/ijcce.1996.10131
VANCOUVER
Khalafy, J., Pruce, J. M. Synthesis of New 10-Arylthioanthralins and Oxidation of Thioanthralins to Their Corresponding Sulfones. Iranian Journal of Chemistry and Chemical Engineering, 1996; 15(1): 1-7. doi: 10.30492/ijcce.1996.10131
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