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Results: 50
Number of items: 50
  • Wanner, M. J., & Koomen, G. J. (2002). A new Synthesis of Temozolomide. Journal of the Chemical Society-Perkin Transactions 1, 2002(16), 1877-1880.
  • Burm, B. E. A., Jongmans, E., van Kampen, E., Wanner, M. J., Koomen, G. J., & Blokker, P. (2001). Synthesis of Xestomanzamines A and B. Heterocycles, 55, 495-503.
  • Wanner, M. J., & Koomen, G. J. (2001). Synthesis and Properties of 2-Nitrosoadenosine. Journal of the Chemical Society-Perkin Transactions 1, I, 1908-1915.
  • Gremmen, C., Wanner, M. J., & Koomen, G. J. (2001). Enantiomerically Pure Isoquinolines via N-sulfinyl Pictet-Spengler reactions. Tetrahedron Letters, 8885-8888.
  • Burm, B. E. A., Gremmen, C., Wanner, M. J., & Koomen, G. J. (2001). Synthesis of New Bridged Tetrahydro-b-Carbolines and Spiro-Fused Quinuclidines. Tetrahedron, 57, 2039-2049. https://doi.org/10.1016/S0040-4020(01)00023-0
  • Deghati, P. Y. F., Bieraugel, H., Wanner, M. J., & Koomen, G. J. (2000). Mild and Regioselective Nitration of 1-Deazapurine Nucleosides using TBAN/TFAA. Tetrahedron Letters, 72, 569-573.
  • Degahti, P. Y. F., Wanner, M. J., & Koomen, G. J. (2000). Regioselective Nitration of 1-Purine Nucleosides; Snthesis of 2-Nitroadenosine and 2-Nitroinosine.Tetrahedron Letters. Tetrahedron Letters, (41), 1291-1295.
  • Gremmen, C., Willemse, B., Wanner, M. J., & Koomen, G. J. (2000). Enantiopure tetrahydro-¿-carbolines via Pictet-Spengler Reactions with N-Sulfinyl Tryptamines. Organic Letters, 2, 955-1958.
  • Wanner, M. J., Von Freitag Drabbe Kunzel, J. C., IJzerman, A. P., & Koomen, G. J. (2000). 2-Nitro analogues of adenosine and 1-deazaadenosine: synthesis and binding studies at the adenosine A1, A2A and A3 receptor subtypes. Bioorganic & Medicinal Chemistry Letters, 10(18), 2141-2144. https://doi.org/10.1016/S0960-894X(00)00415-7
  • Wanner, M. J., & Koomen, G. J. (1997). Biomimetic Syntheses of Racemic Alkaloids. In F. Awouters (Ed.), Proceedings 14th International Symposium on Medicinal Chemistry. F. (pp. 179-187). Elsevier Science BV.
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