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        Synthesis  2007(11): 1624-1628  
DOI: 10.1055/s-2007-966055
   DOI: 10.1055/s-2007-966055
PAPER
© Georg Thieme Verlag Stuttgart · New YorkFacile Preparation of Polyfluoroalkylated Aldimines from Polyfluoroalkanoic Acids
Further Information
            
               
                  
                        
                              Received
                              15 March 2007 
                      
Publication Date:
11 May 2007 (online)
            
         
      
   Publication History
Publication Date:
11 May 2007 (online)

Abstract
Polyfluoroalkylated aldimines were prepared by reducing polyfluoroalkyl imidoyl chlorides, which are readily available from polyfluoroalkanoic acids, with LTBA (lithium tri-tert-butoxyaluminum hydride).
Key words
fluorine - aldimine - imidoyl chloride - reduction - hydride
- β-Lactam:
- 1a 
             
            Enders D.Reinhold U. Tetrahedron: Asymmetry 1997, 8: 1895
- 1b 
             
            Bloch R. Chem. Rev. 1998, 98: 1407
- 1c 
             
            Kobayashi S.Ishitani H. Chem. Rev. 1999, 99: 1069
- Taxol:
- 1d 
             
            Kuznetsova L.Ungureanu IM.Pepe A.Zanardi I.Wu X.Ojima I. J. Fluorine Chem. 2004, 125: 487
- 1e 
             
            Battaglia A.Bernacki RJ.Bertucci C.Bombardelli E.Cimitan S.Ferlini C.Fontana G.Guerrini A.Riva A. J. Med. Chem. 2003, 46: 4822
- Aziridine:
- 1f 
             
            Crousse B.Narizuka S.Bonnet-Delpon D.Begue J.-P. Synlett 2001, 679
- 2a 
             
            Ingrassia L.Mulliez M. Synthesis 1999, 1731
- 2b 
             
            Abouabdellah A.Bégué J.-P.Bonnet-Delpon D.Nga TTT. J. Org. Chem. 1997, 62: 8826
- 2c 
             
            Arnone A.Bruche L.Panzeri W.Pesenti C.Viani F.Zucca C. J. Chem. Res., Synop. 2002, 131
- 2d 
             
            Guanti G.Banfi L.Narisano E.Scolastico C.Bosone E. Synthesis 1985, 609
- 3a 
             
            Henne AL.Pelley RL.Alm RM. J. Am. Chem. Soc. 1950, 72: 3370
- 3b 
             
            Braid M.Iserson H.Lawlor FE. J. Am. Chem. Soc. 1954, 76: 4027
- 3c 
             
            Ogden RP.Thomas GK. J. Am. Chem. Soc. 1954, 76: 300
- 3d 
             
            Husted DR.Ahlbrecht AH. J. Am. Chem. Soc. 1952, 74: 5422
- 3e 
             
            Ono N.Kawamura H.Maruyama K. Bull. Chem. Soc. Jpn. 1989, 62: 3386
- 4 
             
            Tamura K.Mizukami H.Maeda K.Watanabe H.Uneyama K. J. Org. Chem. 1993, 58: 32Reference Ris Wihthout Link
- 5a 
             
            Tanaka M.Kobayashi T. Synthesis 1985, 967
- 5b 
             
            Alper H.Tanaka M. Synthesis 1978, 781
- 5c 
             
            Jousseaume B.Vilcot N.Ricci A.Tiekink ERT. J. Chem. Soc., Perkin Trans. 1 1994, 2283
- 6a 
             
            Karady S.Amato JS.Weinstock LM.Sletzinger M. Tetrahedron Lett. 1978, 403
- 6b 
             
            Luo JK.Zektzer AS.Castle RN. J. Heterocycl. Chem. 1991, 28: 737
 
    