Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
          
          https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000084.xml
        Synthesis  2009(18): 3099-3105  
DOI: 10.1055/s-0029-1216907
   DOI: 10.1055/s-0029-1216907
PAPER
© Georg Thieme Verlag
      Stuttgart ˙ New YorkReaction of N,N-Dioxyenamines with Anhydrides of Carboxylic and Sulfonic Acids; A New Method for the Synthesis of α-Hydroxyoxime Derivatives
Further Information
            
               
                  
                        
                              Received
                              16 April 2009 
                      
Publication Date:
14 July 2009 (online)
            
         
      
   Publication History
Publication Date:
14 July 2009 (online)

Abstract
The reactions of N,N-dioxyenamines with carboxylic and sulfonic acid anhydrides were investigated. A new method for the synthesis of α-hydroxyoxime derivatives via the reaction of N,N-dioxyenamines with trifluoroacetic anhydride is described.
Key words
1,2-oxazine - trifluoroacetic anhydride - hydroxyoxime - enamine - rearrangement
- 1 
             
            Tishkov AA.Lesiv AV.Khomutova YuA.Strelenko YuA.Nesterov ID.Antipin MYu.Ioffe SL.Denmark SE. J. Org. Chem. 2003, 68: 9477
- 2a 
             
            Dilman AD.Tishkov AA.Lyapkalo IM.Ioffe SL.Strelenko YuA.Tartakovsky VA. Synthesis 1998, 181Reference Ris Wihthout Link
- 2b 
             
            Dilman AD.Tishkov AA.Lyapkalo IM.Ioffe SL.Kachala VV.Strelenko YuA.Tartakovsky VA. J. Chem. Soc., Perkin Trans. 1 2000, 2926Reference Ris Wihthout Link
- 3 
             
            Dilman AD.Lyapkalo IM.Ioffe SL.Strelenko YuA.Tartakovsky VA. J. Org. Chem. 2000, 65: 8826
- 4 
             
            Dilman AD.Ioffe SL.Mayr H. J. Org. Chem. 2001, 66: 3196
- 5 
             
            Kunetsky RA.Dilman AD.Struchkova MI.Tartakovsky VA.Ioffe SL. Tetrahedron Lett. 2005, 46: 5203
- 6 
             
            Ustinov AV.Dilman AD.Ioffe SL.Strelenko YuA.Smit WA.Tartakovsky VA. Mendeleev Commun. 2003, 13: 74
- 7 
             
            Dilman AD.Lyapkalo IM.Ioffe SL.Strelenko YuA.Tartakovsky VA. Synthesis 1999, 1767
- 8a 
             
            Feger H.Simchen G. Liebigs Ann. Chem. 1986, 3: 1456Reference Ris Wihthout Link
- 8b 
             
            Makarenkova LM.Bliznets IV.Ioffe SL.Strelenko YuA.Tartakovsky VA. Russ. Chem. Bull. 2000, 49: 1261Reference Ris Wihthout Link
- 8c 
             
            Lesiv AV.Ioffe SL.Strelenko YuA.Tartakovsky VA. Helv. Chim. Acta 2002, 85: 3489Reference Ris Wihthout Link
- 8d 
             
            Semakin AN.Sukhorukov AYu.Lesiv AV.Khomutova YuA.Ioffe SL.Lyssenko KA. Synthesis 2007, 2862Reference Ris Wihthout Link
- 8e 
             
            Lesiv AV.Ioffe SL.Strelenko YuA.Danilenko VM. Russ. Chem. Bull. 2004, 10: 2233Reference Ris Wihthout Link
- 9 
             
            Lesiv AV.Ioffe SL.Strelenko YuA.Bliznets IV.Tartakovsky VA. Mendeleev Commun. 2002, 12: 99
- 10 
             
            Ustinov AV.Dilman AD.Ioffe SL.Belyakov PA.Strelenko YuA. Russ. Chem. Bull. 2002, 8: 1455
- 11 
             
            Sukhorokov AYu.Bliznets IV.Lesiv AV.Khomutova YuA.Strelenko TuA.Ioffe SL. Synthesis 2005, 1077
- 12 
             
            Lee JY.Hong Y.-T.Kim S. Angew. Chem. Int. Ed. 2006, 45: 6182
- 14a 
             
            Tabolin AA.Lesiv AV.Khomutova YuA.Belyakov PA.Strelenko YuA.Ioffe SL. Synthesis 2005, 1656Reference Ris Wihthout Link
- 14b 
             
            Feger H.Simchen G. Liebigs Ann. Chem. 1986, 428Reference Ris Wihthout Link
- 15 
             
            Klenov MS.Lesiv AV.Khomutova YuA.Nesterov ID.Ioffe SL. Synthesis 2004, 1159
- 16 
             
            Tabolin AA.Lesiv AV.Khomutova YuA.Nelyubina YuV.Ioffe SL. Tetrahedron 2009, 65: 4578
- For the substitution of silyl group by trifluoroacetyl see:
- 18a 
             
            Aubert C.Begue J.-P. Synthesis 1985, 759Reference Ris Wihthout Link
- 18b 
             
            Stamatov SD.Stawinski J. Synlett 2007, 439Reference Ris Wihthout Link
- 20a 
             
            Miyata O.Koizumi T.Asai H.Iba R.Naito T. Tetrahedron Lett. 2005, 46: 4015Reference Ris Wihthout Link
- 20b 
             
            Moutel S.Shipman M.Martin OR.Ikedac K.Asano N. Tetrahedron: Asymmetry 2005, 16: 487Reference Ris Wihthout Link
- 20c 
             
            Wan X.Doridot G.Joullie MM. Org. Lett. 2007, 9: 977Reference Ris Wihthout Link
- 21a 
             
            Marco JA.Carda M.Murga J.Rodrigues S.Falomir E.Oliva M. Tetrahedron: Asymmetry 1998, 9: 1679Reference Ris Wihthout Link
- 21b 
             
            Dransfield PJ.Gore PM.Prokes I.Shipman M.Slawin AMZ. Org. Biomol. Chem. 2003, 1: 2723Reference Ris Wihthout Link
- 22a 
             
            Hennebohle M.Le Roy P.-Y.Hein M.Ehrler R.Jager V. Z. Naturforsch., B: Chem. Sci. 2004, 59: 451Reference Ris Wihthout Link
- 22b 
             
            Demir AS.Sesenoglu O.Aksoy-Cam H.Kaya H.Aydogan K. Tetrahedron: Asymmetry 2003, 14: 1335Reference Ris Wihthout Link
- 23a 
             
            Tsoungas PS. Heterocycles 2002, 57: 915Reference Ris Wihthout Link
- 23b 
             
            Zimmer R.Collas M.Czerwonka R.Hain U.Reissig H.-U. Synthesis 2008, 237Reference Ris Wihthout Link
- 24 
             
            Gottlieb HE.Kotlyar V.Nudelman A. J. Org. Chem. 1997, 62: 7512
- 25 
             
            Almarego WLF.Chai CLL. In Purification of Laboratory Chemicals 5th ed.: Elsevier; Oxford: 2003. p.370
- 26 
             
            Kunetsky RA.Dilman AD.Struchkova MI.Belyakov PA.Tartakovsky VA.Ioffe SL. Synthesis 2006, 2265
- 27 
             
            Kunetsky RA.Dilman AD.Ioffe SL.Struchkova MI.Strelenko YuA.Tartakovsky VA. Org. Lett. 2003, 5: 4907
References
For BENA nucleophilicity parameter N = 3-5 according to Professor Mayr’s scale, while for ‘classical’ enamines N = ≥ 11 (ref. 4).
17Mikhailov, A. A.; Lesiv, A. V.; Ioffe, S. L. unpublished.
19For discussion of the stereochemistry of the rearrangement of 2 see ref. 16.
 
    