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The Microbiological Reduction/Oxidation Concept: An Approach to a Chemoenzymatic Preparation of Optically Pure Lactones and Lactonic Synthons

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Bioorganic Chemistry in Healthcare and Technology

Part of the book series: NATO ASI Series ((NSSA,volume 207))

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Abstract

In the recent years, intensive work has been devoted to the efficient preparation of new chiral synthons by asymmetric transformation of prochiral molecules, through enzymic or microbiological catalysis. In this respect, we have developed combined chemical- microbiological reduction and oxidation (Baeyer-Villiger like) methods which allow to obtain either enantiomer of chiral substituted lactones and lactonic synthons.

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References

  1. D. Buisson, R. Azerad, G. Revial and J. D’Angelo, Tetrahedron Lett., 25 (1984) 6005

    Article  CAS  Google Scholar 

  2. J. D’Angelo, G. Revial, R. Azerad and D. Buisson, J. Org. Chem., 51 (1986) 40.

    Article  Google Scholar 

  3. J. Ouazzani-Chahdi, D. Buisson and R. Azerad, Tetrahedron Lett., 28 (1987) 1109.

    Article  CAS  Google Scholar 

  4. P.R. Atkinson, J. Entomol. Soc. South Afr., 43 (1980) 171.

    Google Scholar 

  5. J.P. Vigneron, R. Méric, M. Larchevêque, A. Debal, G. Kunesch, P. Zagatti and M. Gallois, Tetrahedron Lett., 23 (1982) 5051

    Article  CAS  Google Scholar 

  6. T. Uematsu, T. Umemura and K. Mori, AgricBiol. Chem., 47 (1983) 597

    Article  CAS  Google Scholar 

  7. J.P. Vigneron, R. Méric, M. Larchevêque, A. Debal, J.Y. Lallemand, G. Kunesch, P. Zagatti and M. Gallois, Tetrahedron, 40 (1984) 3521

    Article  CAS  Google Scholar 

  8. K. Suzuki, T. Ohkuma, G. Tsuchihashi, Tetrahedron Lett., 26 (1985) 861

    Article  CAS  Google Scholar 

  9. H.G. Davies, S.M. Roberts, B.J. Wakefield and J.A. Winders, J. Chem. Soc. Chem. Commun., (1985) 1166

    Google Scholar 

  10. H. Frauenrath and T. Philipps, Tetrahedron, 42 (1986) 1135

    Article  CAS  Google Scholar 

  11. R.M. Ortuno, R. Mercé and J. Font, Tetrahedron Lett., 27 (1986) 2519

    Article  CAS  Google Scholar 

  12. D.S. Matteson, K.M. Sadhu and M.L. Petterson, J. Am. Chem. Soc., 108 (1986) 810.

    Article  CAS  Google Scholar 

  13. R.D. Stolow, P.M. McDonagh and M.M. Bonaventura, J. Am. Chem. Soc., 86 (1964)2165.

    Article  CAS  Google Scholar 

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© 1991 Plenum Press, New York

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Azerad, R., Buisson, D., Maillot, S., Ouazzani-Chahdi, J. (1991). The Microbiological Reduction/Oxidation Concept: An Approach to a Chemoenzymatic Preparation of Optically Pure Lactones and Lactonic Synthons. In: Pandit, U.K., Alderweireldt, F.C. (eds) Bioorganic Chemistry in Healthcare and Technology. NATO ASI Series, vol 207. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-1354-0_20

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  • DOI: https://doi.org/10.1007/978-1-4684-1354-0_20

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4684-1356-4

  • Online ISBN: 978-1-4684-1354-0

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