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Results: 200
Number of items: 200
  • Briere, J.-F. B. P., Blaauw, R. H., Benningshof, J. C. J., van Ginkel, A. E., van Maarseveen, J. H., & Hiemstra, H. (2001). Synthesis of the right-hand substructure of solanoeclepin A. European Journal of Organic Chemistry, 2371-2377.
  • Open Access
    Benningshof, J. C. J. (2001). Studies towards the total synthesis of solanoeclepin A: synthesis of analogues containing the tetracyclic left-hand substructure. [Thesis, fully internal, Universiteit van Amsterdam].
  • Open Access
    Blaauw, R. H. (2001). Intramolecular [2+2]photocycloadditions as an approach towards the right-hand side of solanoeclepin A. [Thesis, fully internal, Universiteit van Amsterdam].
  • Open Access
    Diederen, J. J. H. (2001). Palladium mediated synthesis of N-heterocycles by iminoannulation of allenes. [Thesis, fully internal, Universiteit van Amsterdam].
  • Tjen, K. C. M. F., Kinderman, S. S., Hiemstra, H., & Rutjes, F. P. J. T. (2000). A ring-closing metathesis-mediated route to novel enantiopure conformationally restricted cyclic amino acids. Chemical Communications, 699-700.
  • Jonasson, C., Karstens, W. F. J., Hiemstra, H., & Backvall, J. E. (2000). Palladium(II)-catalyzed intramolecular 1,2-oxidation of allenes involving nitrogen nucleophiles. Tetrahedron Letters, 41, 1619-1622. https://doi.org/10.1016/S0040-4039(99)02343-6
  • Ostendorf, M., Dijkink, J., Rutjes, F. P. J. T., & Hiemstra, H. (2000). (S)-Pyroglutamic acid, (S)-malic acid and (S)-serine as useful starting materials in the synthesis of enantiopure hydroxyamidines. European Journal of Organic Chemistry, 115-124.
  • Ostendorf, M., van der Neut, R., Rutjes, F. P. J. T., & Hiemstra, H. (2000). Enantioselective synthesis of hydroxy-substituted DBN-type amidines as potential chiral catalysts. European Journal of Organic Chemistry, 105-114.
  • Blaauw, R. H., Briere, J.-F. B. P., de Jong, R., Benningshof, J. C. J., van Ginkel, A. E., Rutjes, F. P. J. T., Fraanje, J., Goubitz, K., Schenk, H., & Hiemstra, H. (2000). Intramolecular [2+2] photocycloadditions as an approach towards the bicyclo[2.1.1]hexane substructure of solanoeclepin A, Chem. Commun. Chemical Communications, 16, 1463-1464.
  • Bamford, S. J., Goubitz, K., van Lingen, H., Luker, T. J., Schenk, H., & Hiemstra, H. (2000). Formation of medium-size bridged ring systems via ring-closing metathesis of 2,5-disubstituted-2,3-dihydro-1H-pyrroles. Journal of the Chemical Society-Perkin Transactions 1, 1(3), 345-351.
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