References
- Keiichi , S. , Toru , O. and Aki , S. Preparation of aromatic sulfones from sulfinic acids and halides . JP Patent 04120050 . 1992 .
- Caron , G. , Gaillard , P. , Carrupt , P. A. and Testa , B. 1997 . Lipophilicity behavior of model and medicinal compounds containing a sulfide, sulfoxide or sulfone moiety . Helv. Chim. Acta , 80 : 449
- Sun , Z. , Botros , E. , Su , A. , Kim , Y. , Wang , E. , Baturay , N. Z. and Kwon , C. 2000 . Sulfoxide‐containing aromatic nitrogen mustards as hypoxia‐directed bioreductive cytotoxins . J. Med. Chem. , 43 : 4160
- Tashiaki , T. and Takeshi , Y. Heat‐sensitive recording material with excellent coloring and printed image stability . JP Patent 2001260544 . 2001 .
- Tobe , A. , Fujimori , S. , Yamazaki , T. , Sugano , M. , Kikumoto , R. and Nitta , I. Aryl sulfone compounds . EP Patent 194669 . 1986 .
- Merchant , J. R. , Koshti , N. M. and Gupta , A. S. 1982 . Synthesis of sulfones with antitubercular activity . Chem. Ind. , 23 : 955
- Fournier , J. P. , Loiseau , P. , Moreau , R. C. , Narcisse , G. and Choay , P. 1982 . Hypolipemic activity of 2‐hydroxyalkyl and 3‐hydroxyalkyl phenyl sulfones . Eur. J. Med. Chem. Chim. Ther. , 17 : 53
- Mehta , K. J. , Parekh , H. H. and Parikh , A. R. 1988 . Preparation and antimicrobial activity of bis‐(p‐thiazolidinonphrnyl sulfones and α‐(carboxyphenylamino)benzyl aryl sulfides and sulfones . J. Inst. Chem. , 60 : 153
- Giordano , C. , Cavicchioli , S. , Levi , S. and Villa , M. 1991 . Direct conversion of (1s,2s)‐2‐amino‐1‐[(4‐methylthio)phenyl]‐1,3‐propanediol into its enantiomer for efficient synthesis of thiamphenicol and florfenicol . J. Org. Chem. , 56 : 6114
- McMahon , J. B. , Gulakowski , R. J. , Weislow , O. S. , Schultz , R. J. , Narayanan , V. L. , Clanton , D. J. , Pedemonte , R. , Wassmundt , F. W. , Buckheit , R. W. Jr. , Decker , W. D. , White , E. L. , Bader , J. P. and Boyd , M. R. 1993 . Diarylsulfones, a new chemical class of nonnucleoside antiviral inhibitors of human immunodeficiency virus type I release transcriptase . Antimicrob. Agents Chemther. , 37 : 754
- Williams , T. M. , Ciccarone , T. M. , MacTough , S. C. , Rooney , C. S. , Balani , S. K. , Condra , J. H. , Emini , E. A. , Goldman , M. E. , Greenlee , W. J. , Kauffman , L. R. , O'Bnen , J. A. , Sardana , V. V. , Schleif , W. A. , Theoharides , A. D. and Anderson , P. S. 1993 . 5‐chloro‐3‐(phenylsulfonyl)indole‐2‐carboxamide: A novel, non‐nucleoside inhibitor of HIV‐1 reverse transcriptase . J. Med. Chem. , 36 : 1291
- Neamati , N. , Mazumder , A. , Zhao , H. , Sunder , S. , Burke , T. R. Jr. , Schultz , R. J. and Pommier , Y. 1997 . Diarylsulfones, a novel class of human immunodeficiency virus type I integrase inhibitors . Antimicrob. Agents Chemther. , 41 : 385
- Degterev , A. , Lugovskoy , A. , Cardone , M. , Mulley , B. , Wagner , G. , Mitchison , T. and Yuan , J. Y. 2001 . Identification of small‐molecule inhibitors of interaction between the BH3 domain and Bcl‐XL . Nature Cell Biology , 3 : 173
- Feng , W. Y. , Liu , F. T. , Patwari , Y. , Agrawal , S. G. , Newland , A. C. and Jia , L. 2003 . BH3‐domain mimetic compound BH3I‐2' induces rapid damage to the inner mitochondria1 membrane prior to the cytochrome c release from mitochondria . Br. J. Haematol. , 121 : 332
- Gilman , H. , Beaver , N. J. and Meyers , C. H. 1925 . The reaction between aryl sulfonates and organomagnesium halides . J. Am. Chem. Soc. , 47 : 2047
- Baarschers , W. H. 1976 . Reactions of organolithium compounds with sulfonate esters. A novel sulfone synthesis . Can. J. Chem. , 54 : 3056
- Ueda , M. , Uchiyama , K. and Kano , T. 1984 . A new synthesis of diaryl sulfones . Synthesis , : 323
- Turpin , J. A. , Song , Y. , Inman , J. K. , Huang , M. , Wallqvist , A. , Maynard , A. , Covell , D. G. , Rice , W. G. and Appella , E. 1999 . Synthesis and biological properties of novel pyridinioalkanoylthiolesters (PATE) as Anti‐HIV‐1 agents that target the viral nucleocapsid protein zinc fingers . J. Med. Chem. , 42 : 67
- Sato , K. , Hyodo , M. , Aoki , M. , Zheng , X. and Noyori , R. 2001 . Oxidation of sulfides to sulfoxides and sulfones with 30% hydrogen peroxide under organic solvent‐ and halogen‐free conditions . Tetrahedron , 57 : 2469
- Shaabani , A. , Teimouri , F. and Lee , D. G. 2003 . Ion exchange catalysis in oxidation of organic compounds with KMnO4 . Synth. Commun. , 33 : 1057
- Adams , R. , Reifschneider , W. and Ferretti , A. 1973 . 1,2‐bis(n‐butylthio)benzene . Org. Synth. Coll. , V : 107
- Lu , C. , Huges , E. W. and Giguere , P. A. 1941 . The crystal structure of Urea‐hydrogen peroxide addition compound CO(NH2)2 · H2O2 . J. Am. Chem. Soc. , 53 : 1507
- Courtin , A. 1983 . Notiz zur synthese von alkyl‐, cycloalkyl‐ und aryl‐(4‐aminophenyl)‐ sulfonen . Helv. Chim. Acta , 66 : 1046
- Hammick , D. L. and Williams , R. B. 1938 . The mesomeric effect of the sulphoxide group . J. Chem. Soc. , : 211
- Nose , M. and Suzuki , H. 2002 . Convenient one‐pot procedure for converting aryl sulfides to nitroaryl sulfones . Synthesis , 8 : 1065
- Loudon , J. D. 1936 . The action of sulphinates on 2,4‐dinitrodiphenylsulphones . J. Chem. Soc. , : 218
- Heppenstall , M. E. and Smiles , S. 1938 . Aromatic hydroxy‐sulphones . J. Chem. Soc. , : 899
- Moore , G. G. and Harrington , J. C. 1972 . “ Fluoroalkylsulfonamidoaryl compounds as plant growth regulators ” . Ger. Offen 2118190, (Chem. Abstr. 1972, 77, 19402u)