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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 35, 2005 - Issue 8
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Original Articles

Reaction of Active Methylene Groups with 1,2‐Di(Bromoseleno)Benzene toward Benzo‐1,3(2H)‐Diselenoles

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Pages 1077-1083 | Received 08 Dec 2004, Published online: 16 Aug 2006

References

  • Paulmier , C. 1986 . Selenium Reagents and Intermediates in Organic Synthesis Oxford : Pergamon Press .
  • Tiecco , M. 2000 . Electrophilic selenium, selenocyclizations . Topics Curr. Chem. , 208 : 7 – 54 .
  • Iwaoka , M. and Tomoda , S. 1994 . “ Benzeneselenenyl chloride ” . In Encyclopedia of Reagents for Organic Synthesis Edited by: Paquette , L. Vol. 1 , 261 – 265 . Chichester : Wiley .
  • Procter , D. J. 2000 . The synthesis of thiols, selenols, sulfides, selenides, sulfoxides, selenoxides, sulfones and selenones . J. Chem. Soc. Perkin Trans 1 , 6 : 835 – 871 .
  • Wirth , T. 1999 . Chiral selenium compounds in organic synthesis . Tetrahedron , 55 ( 1 ) : 1 – 28 .
  • Mugesh , G. and Singh , H. B. 2000 . Synthetic organoselenium compounds as an tioxidants: Glutathione peroxidase activity . Chem. Soc. Rev. , 29 ( 5 ) : 347 – 357 .
  • Mugesh , G. , du Mont , W.‐W. and Sies , H. 2001 . Chemistry of biologically important synthetic organoselenium compounds . Chem. Rev. , 101 ( 7 ) : 2125 – 2179 .
  • Młochowski , J. , Brza¸szcz , M. , Giurg , M. , Palus , J. and Wójtowicz , H. 2003 . Selenium‐promoted oxidation of organic compounds: reaction and mechanisms . Eur. J. Org. Chem. , 22 : 4329 – 4339 .
  • Młochowski , J. , Kloc , K. , Syper , L. , Inglot , A. D. and Piasecki , E. 1993 . Aromatic and azaaromatic diselenides, benzisoselenazolones and related compounds as immunomodulators active in humans: Synthesis and properties . Liebigs Ann. Chem. , 12 : 1293 – 1244 .
  • Młochowski , J. , Gryglewski , R. , Inglot , A. D. , Jakubowski , A. , Juchniewicz , L. and Kloc , K. 1996 . Synthesis and properties of 2‐carboxyalkyl‐1,2‐benzisoselenazol‐3(2H)‐ones and related organoselenium compounds as nitric oxide synthase inhibitors and cytokine inducers . Liebigs Ann. Chem. , 11 : 1751 – 1755 .
  • Kloc , K. , Maliszewska , I. and Młochowski , J. 2003 . Synthesis of 7‐azabenzisoselenazol‐3(2H)‐ones: A new group of selenium containing antimicrobials . Synth. Commun. , 33 ( 21 ) : 3805 – 3815 .
  • Kloc , K. and Młochowski , J. 1999 . Synthesis of organoselenium sulfonamides as new potential cytokine inducers: 2,2′‐diselenobis(benzenesulfonamides) and and 1,3,2‐benzenethiaselenazole 1,1,‐dioxides . Eur. J. Org. Chem. , 1 : 67 – 71 .
  • Kloc , K. and Młochowski , J. 2001 . Selenylation‐acylation of ketones with 2‐chloroselenobenzoyl chloride: A novel route to benzo[b]selenophenes . Tetrahedron Lett. , 42 ( 29 ) : 4899 – 4902 .
  • Kloc , K. , Młochowski , J. , Osajda , K. , Syper , L. and Wójtowicz , H. 2002 . New heterocyclic selenenamides: 1,2,4‐benzoselenadiazin‐3(4H)‐ones and 1,3,2‐benzodiselenazoles . Tetrahedron Lett. , 43 ( 22 ) : 4071 – 4074 .
  • Giurg , M. and Młochowski , J. 1999 . Oxidative ring contraction of cycloalkanones: A facile method for synthesis of medium ring cycloalkanecarboxylic acids . Synth. Commun. , 29 ( 13 ) : 2281 – 2291 .
  • Lambert , C. and Christiaens , L. 1984 . Alternative syntheses of dibenzotetraselenafulvalene, of some of its precursors and of tetraselenoalkenes analogs . Tetrahedron Lett. , 25 ( 8 ) : 833 – 834 .

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