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        Synthesis  2001(9): 1308-1310
DOI: 10.1055/s-2001-15232
   DOI: 10.1055/s-2001-15232
SHORTPAPER
© Georg Thieme Verlag Stuttgart · New YorkA Convenient Synthesis of Selenocarboxamides from Nitriles
Further Information
            
               
                  
                        
                              Received
                              5 February 2001 
                      
Publication Date:
29 September 2004 (online)
            
         
      
   Publication History
Publication Date:
29 September 2004 (online)

Abstract
Aromatic and aliphatic nitriles can be conveniently converted into the corresponding selenocarboxamides with monoselenophosphate in aqueous alcohol in 50-94 % yield.
Key words
monoselenophosphate - nitriles - selenocarboxamides
- 1 
             
            Dell CP. In Comprehensive Organic Functional Group Transformations Vol. 5:Moody CJ. Elsevier; Oxford: 1995. p.565-628Reference Ris Wihthout Link
- 2 
             
            Cohen VI. Synthesis 1978, 668
- 3 
             
            Ogawa A.Miyake J.Karasaki Y.Murai S.Sonoda N. J. Org. Chem. 1985, 50: 384
- 4 
             
            Lai L.-L.Reid DH. Synthesis 1993, 870
- 5 
             
            Zhao X.-R.Ruan M.-D.Fan W.-Q.Zhou XJ. Synth. Commun. 1994, 24: 1761
- 6 
             
            Shimada K.Hikage S.Takeishi Y.Takikawa Y. Chem. Lett. 1990, 1403
- 7 
             
            Ishikara H.Yosimura K.Konketsu M. Chem. Lett. 1998, 1287
- 8 
             
            Ruan M.-D.Zhang P.-F.Tao Y.Fan W.-Q. Synth. Commun. 1996, 26: 2617
- 9 
             
            Shimada K.Jin N.Kawaguchi M.Dobashi K.Nagano Y.Fujimura M.Kudoh E.Kai T.Saito N.Masuda J.Iwaya M.Fujisawa H.Aoyagi S.Takikawa Y. Bull. Chem. Soc. Jpn. 1997, 70: 197
- 10 
             
            Li GM.Zingaro RA.Segi M.Reibenspies JH.Nakajima T. Organometallics 1997, 16: 756
- 11 
             
            Li GM.Zingaro RA. J. Chem. Soc., Perkin Trans. 1 1998, 647
- 12 
             
            Hartmann H. Z. Chem. 1971, 11: 60
- 13 
             
            Cohen VI. J. Org. Chem. 1977, 42: 2645
- 14 
             
            Sukhai RS.deJong R.Brandsma L. Synthesis 1977, 888
- 15 
             
            Malek-Yazdi F.Yalpani M. Synthesis 1977, 328
- 16 
             
            Murai T.Ezaka T.Niwa N.Kanda T.Kato S. Synlett 1996, 865
- 17 
             
            Murai T.Ezaka T.Kanda T.Kato S. Chem. Commun. 1996, 1809
- 18 
             
            Otten PA.van derGen A. Recl. Trav. Chim. Pays-Bas 1994, 113: 499
- 19 
             
            Okuma K.Ikari K.Ohta H. Chem. Lett. 1992, 131
- 20 
             
            Kamiñski R.Glass RS.Schroeder TB.Michalski J.Skowroñska A. Bioorg. Chem. 1997, 25: 247
- 21 
             
            Kindel K. Liebigs Ann. Chem. 1923, 431: 187
- 22 
             
            Miko M.ajczyk Kie P.basiñski Basiñski W. J. Org. Chem. 1984, 49: 899
- 23 
             
            Azman A.Drofenik N.Hadzi D.Lukman B. J. Mol. Struct. 1968, 1: 181
- 24 
             
            Stadtman TC.Glass RS. Meth. Enzymol. 1995, 252: 309
- 25 
             
            Borecka B.Chojnowski J.Cypryk M.Michalski J.Zieliñska J. J. Organomet. Chem. 1979, 171: 17
 
    