Chameleon catches in combinatorial chemistry: Tebbe olefination of polymer supported esters and the synthesis of amines, cyclohexanones, enones, methyl ketones and thiazoles

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Christopher P. Ball, Anthony G. M. Barrett, Delphine Compère, Cyrille Kuhn, Richard S. Roberts, Marie L. Smith, Olivier Venier and Alain Commerçon


Abstract

Tebbe olefination of supported esters R1CO2CH2–polymer gave the corresponding vinyl ethers R1C([double bond, length half m-dash]CH2)OCH2–polymer which were released, under acidic conditions, to produce methyl ketones R1COMe; by reductive amination, to produce amines R1CH(Me)NHR2; by bromination and reaction of R1CBr(CH2Br)OCH2-polymer with thioureas to produce thiazoles; or, for supported dienyl ethers derived from α,β-unsaturated esters, by Diels–Alder reaction and acid mediated cleavage to produce cyclohexanone derivatives.


References

  1. For examples see: P. H. H. Hermkens, H. C. J. Ottenheijm and D. C. Rees, Tetrahedron, 1997, 53, 5643 Search PubMed; S. H. D. J. Gravert and K. D. Janda, Chem. Rev., 1997, 97, 489 CrossRef CAS; L. A. Thompson and J. A. Ellman, Chem. Rev., 1996, 96, 555 CrossRef CAS.
  2. J.-P. Montheard, M. Chatzopoulos and M. Camps, J. Macromol. Sci., Rev. Macromol. Chem. Phys., 1988, C28, 503 Search PubMed; V. Krchnak, D. Cabel, A. Weichsel and Z. Flegelova, Lett. Pept. Sci., 1995, 1, 27 Search PubMed; M. Bodanszky and D. T. Fagan, Int. J. Pept. Protein Res., 1977, 10, 375 Search PubMed.
  3. F. Effenberger, Angew. Chem., Int. Ed. Engl., 1969, 8, 295 CrossRef CAS.
  4. S. H. Pine, R. Zahler, D. A. Evans and R. H. Grubbs, J. Am. Chem. Soc., 1980, 102, 3270 CrossRef CAS.
  5. L. F. Cannizzo and R. H. Grubbs, J. Org. Chem., 1985, 50, 2386 CrossRef CAS.
  6. N. Petasis and E. I. Bzowej, J. Am. Chem. Soc., 1990, 112, 6392 CrossRef CAS.
  7. A. F. Abdel-Magid, K. G. Carson, B. D. Harris, C. A. Maryanoff and R. D. Shah, J. Org. Chem., 1996, 61, 3849 CrossRef CAS; C. G. Boojamra, K. M. Burow and J. A. Ellman, J. Org. Chem., 1995, 60, 5742 CrossRef CAS.
  8. P. C. Kearney, M. Fernandez and J. A. Flygare, J. Org. Chem., 1998, 63, 196 CrossRef CAS and references cited therein.
  9. S. Kobayashi and M. Moriwaki, Tetrahedron Lett., 1997, 38, 4251 CrossRef CAS.
  10. C. R. Johnson and B. Zhang, Tetrahedron Lett., 1995, 36, 9253 CrossRef CAS; P. Wipf and T. C. Henninger, J. Org. Chem., 1997, 62, 1586 CrossRef CAS.
  11. M. Adeva, E. Caballero, F. Garcia, M. Medarde, H. Sahagun and F. Tome, Tetrahedron Lett., 1997, 38, 6893 CrossRef CAS.
  12. M. Crawshaw, N. W. Hird, K. Irie and K. Nagai, Tetrahedron Lett., 1997, 38, 7115 CrossRef CAS.
  13. G. H. Posner, T. D. Nelson, C. M. Kinter and K. Afarinkia, Tetrahedron Lett., 1991, 32, 5295 CrossRef CAS; B. M. Trost and G. K. Mikhail, J. Am. Chem. Soc., 1987, 109, 4124 CrossRef CAS; E. Schaumann and A. Kirschning, Tetrahedron Lett., 1988, 29, 4281 CrossRef CAS; D. H. R. Barton, L. Bohe and X. Lusinchi, Tetrahedron Lett., 1987, 28, 6609 CrossRef CAS; A. Padwa, W. Dent and P. E. Yeske, J. Org. Chem., 1987, 52, 3944 CrossRef CAS; A. G. M. Barrett, Chimica, 1982, 36, 248 Search PubMed.
  14. M. R. Gowravaram and M. A. Gallop, Tetrahedron Lett., 1997, 38, 6973 CrossRef CAS.
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