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Organic synthesis

The Wittig reaction cleans up

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The formation of a phosphine oxide with its strong P=O bond is the driving force for the classical Wittig reaction, but is wasteful and can pose problems during purification. A new development allowing the use of catalytic phosphorus reagents promises to clean up olefination chemistry.

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Figure 1: The development of a catalytic Wittig reaction.

References

  1. Johnson, A. W. Ylides and Imines of Phosphorus (Wiley, 1993).

    Google Scholar 

  2. Pommer, H. Angew. Chem. Int. Ed. Engl. 16, 423–492 (1977).

    Article  Google Scholar 

  3. O'Brien, C. J. et al. Angew. Chem. Int. Ed. 48, 6836–6839 (2009).

    Article  CAS  Google Scholar 

  4. Wittig, G. & Geissler, G. Liebigs Ann. Chem. 580, 44–57 (1953).

    Article  CAS  Google Scholar 

  5. Staudinger, H. & Meyer, J. Helv. Chim. Acta 2, 635 (1919).

    Article  CAS  Google Scholar 

  6. Campbell, T. W., Monagle, J. J. & Foldi, V. S. J. Am. Chem. Soc. 84, 3673–3677 (1962).

    Article  CAS  Google Scholar 

  7. McGonagle, A. E., Marsden, S. P. & McKeever-Abbas, B. Org. Lett. 10, 2589–2591 (2008).

    Article  Google Scholar 

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Marsden, S. The Wittig reaction cleans up. Nature Chem 1, 685–687 (2009). https://doi.org/10.1038/nchem.458

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