CrossRef enabled

PAC Archives

Archive →

Pure Appl. Chem., 2007, Vol. 79, No. 11, pp. 2047-2057

http://dx.doi.org/10.1351/pac200779112047

Electrolysis for the benign conversion of renewable feedstocks

Hans J. Schäfer, Michael Harenbrock, Elisabeth Klocke, Mark Plate and Andreas Weiper-Idelmann

Institute of Organic Chemistry, University of Münster, D-48149 Münster, Correns-Strasse 40, Germany

References

  • 1. E. J. Corey, X.-M. Cheng. The Logic of Chemical Synthesis, John Wiley, New York (1989).
  • 2. J. Fuhrhop, G. Penzlin. Organic Synthesis, 2nd ed., VCH, Weinheim (1994).
  • 3. H. Lund, O. Hammerich (Eds.). Organic Electrochemistry, 4th ed., Marcel Dekker, New York (2001).
  • 4. H. J. Schafer (Ed.). Organic Electrochemistry, Vol. 8 in Encyclopedia of Electrochemistry, A. J. Bard, M. Stratmann (Eds.), Wiley-VCH, Weinheim (2004).
  • 5. (a). H. Lund. Organic Electrochemistry, 4th ed., H. Lund, O.Hammerich (Eds.), Chap. 5, Marcel Dekker, New York (2001);
  • 5. (b). J. Jorissen. Chap. 2 in H.J.Schafer (Ed.), Organic Electrochemistry, Vol. 8 in Encyclopedia of Electrochemistry, A. J. Bard, M. Stratmann (Eds.), Wiley-VCH, Weinheim (2004);
  • 5. (c). H. Putter. Organic Electrochemistry, 4th ed., H. Lund, O.Hammerich (Eds.), Chap. 31, Marcel Dekker, New York (2001).
  • 6. (a). H. J. Schafer. Top. Curr. Chem. 152, 91 (1990);
  • 6. (b). S. Torii, H. Tanaka. In Organic Electrochemistry, 4th ed., H. Lund, O. Hammerich (Eds.), Chap. 14, Marcel Dekker, New York (2001).
  • 7. M. aus dem Kahmen, H. J. Schafer, A. Weiper. Acta Chem. Scand., Ser. B 52, 672 (1998).
  • 8. H. J. Schafer, U. Jensen-Korte. Liebigs Ann. Chem. 1532 (1982).
  • 9. A. Weiper, H. J. Schafer. Angew. Chem. 29, 195 (1990). (http://dx.doi.org/10.1002/anie.199001951)
  • 10. S. Torii. Electroorganic Reduction Synthesis, Chap. 12, Wiley-VCH, Weinheim (2006).
  • 11. S. Kratschmer, H. J. Schafer, R. Frohlich. J. Electroanal. Chem. 507, 2 (2001). (http://dx.doi.org/10.1016/S0022-0728(01)00470-3)
  • 12. W. J. Dejarlais, L. E. Gast, J. C. Cowan. J. Am. Oil Chem. Soc. 50, 108 (1973). (http://dx.doi.org/10.1007/BF02633559)
  • 13. F. D. Gunstone, J. L. Harwood, F. B. Padley. The Lipid Handbook, pp. 11, 244, Chapman and Hall, London (1986).
  • 14. A. E. de Nooy, A. C. Besemer, H. van Bekkum. Synthesis 1153 (1996). (http://dx.doi.org/10.1055/s-1996-4369)
  • 15. S. D. Rychnovsky, R. Vaidyanathan, T. Beauchamp, R. Lin, P. J. Farmer. J. Org. Chem. 64, 6745 (1999). (http://dx.doi.org/10.1021/jo990636c)
  • 16. K. Schnatbaum, H. J. Schafer. Synthesis 864 (1999). (http://dx.doi.org/10.1055/s-1999-3464)
  • 17. M. Schamann, H. J. Schafer. Eur. J. Org. Chem. 351 (2003). (http://dx.doi.org/10.1002/ejoc.200390041)
  • 18. M. Schamann, H. J. Schafer. Electrochim. Acta 50, 4956 (2005). (http://dx.doi.org/10.1016/j.electacta.2005.02.077)
  • 19. P. T. Anastas, J. C. Warner. Green Chemistry, p. 30, Oxford University Press, Oxford (1998).
  • 20. M. Harenbrock, A. Matzeit, H. J. Schafer. Liebigs Ann. 55 (1996).
  • 21. X-ray structure by R. Frohlich. Organisch-Chemisches Institut, Universitat Munster in L. Klocke. Ph.D. thesis, University of Munster (1992).
  • 22. M. Plate. Ph.D. thesis, University of Munster (1997).