Diastereoselective asymmetric cyclopropanation of (S)-(+)-α-(diethoxyphosphoryl)vinyl p-tolyl sulfoxide

(Note: The full text of this document is currently only available in the PDF Version )

Wanda H. Midura, Jerzy A. Krysiak, Marian Mikołajczyk, Michał W. Wieczorek and Wiesław R. Majzner


Abstract

The title sulfoxide 1 reacts with fully deuterated dimethylsulfoxonium methylide, diphenylsulfonium isopropylide and diphenyldiazomethane to form the corresponding cyclopropanes 4 as single diastereoisomers; the chirality of the cyclopropane (+)-4c obtained from 1 and diphenyldiazomethane is (SS,SC) as determined by X-ray diffraction analysis; based on experimental data, the steric course of the asymmetric cyclopropanation is proposed.


References

  1. M. Mikołajczyk, J. Drabowicz and P. Kiełbasiński, Chiral Sulfur Reagents: Applications in Asymmetric and Stereoselective Synthesis, CRC Press, Boca Raton, 1997 Search PubMed.
  2. A.-H. Li, L.-X. Dai and V. K. Aggarwal, Chem. Rev., 1997, 97, 2341 CrossRef CAS.
  3. M. Mikołajczyk and W. H. Midura, Tetrahedron: Asymmetry, 1992, 3, 1515 CrossRef CAS.
  4. W. H. Midura and M. Mikołajczyk, Phosphorus, Sulfur, Silicon, 1994, 95–96, 397.
  5. H. U. Reissig, in The Chemistry of Cyclopropyl Group, ed. S. Patai and Z. Rappoport, Wiley, New York 1987, ch. 8 Search PubMed; H. W. Liu and C. T. Walsh, idem, ch. 16 Search PubMed; J. Salaün and M. S. Baird, Curr. Med. Chem., 1995, 2, 511 Search PubMed.
  6. Ch. Hamdouchi, Tetrahedron Lett., 1992, 33, 1701 CrossRef CAS.
  7. T. Imanishi, T. Ohara, K. Sugiyama, Y. Ueda, Y. Takemoto and C. Iwata, J. Chem. Soc., Chem. Commun., 1992, 296 RSC.
  8. E. J. Corey and M. Jautelat, J. Am. Chem. Soc., 1967, 89, 3912 CrossRef CAS.
  9. J. Drabowicz, B. Dudziński, M. Mikołajczyk, S. Colonna and N. Gaggero, Tetrahedron: Asymmetry, 1997, 13, 2267 CrossRef CAS and references cited therein.
Click here to see how this site uses Cookies. View our privacy policy here.