北海道大学大学院 薬学研究院 創薬科学研究教育センター 有機合成医薬学部門

研究業績

発表論文 2005年

  1. Synthesis of 4,8-anhydro-D-glycero-D-ido-nonanitol 1,6,7-triphosphate as a novel IP3 receptor ligand using a stereoselective radical cyclization reaction based on a conformational restriction strategy.

    Terauchi, M.; Yahiro, Y.; Abe, H.; Ichikawa, S.; Tovey, S. C.; Dedos, S. G.; Taylor, C. W.; Potter, B. V. L.; Matsuda, A.; Shuto, S.

    Tetrahedron 2005, 61, 3697-3707. DOI: 10.1016/j.tet.2005.02.025

  2. Total synthesis of caprazol, a core structure of the caprazamycin antituberculosis antibiotics.

    Hirano, S.; Ichikawa, S.; Matsuda, A.

    Angew. Chem., Int. Ed. 2005, 44, 1854-1856. DOI: 10.1002/anie.200462439

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  3. Synthesis of stable and cell-type selective analogues of cyclic ADP-ribose, a Ca2+-mobilizing second messenger. Structure-activity relationship of the N1-ribose moiety.

    Kudoh, T.; Fukuoka, M.; Ichikawa, S.; Murayama, T.; Ogawa, Y.; Hashii, M.; Higashida, H.; Kunerth, S.; Weber, K.; Guse, A. H.; Potter, B. V. L.; Matsuda, A.; Shuto, S.

    J. Am. Chem. Soc. 2005, 127, 8846-8855. DOI: 10.1021/ja050732x

  4. Synthesis of galactose-linked uridine derivatives with simple linkers as potential galactosyltransferase inhibitors.

    Murata, S.; Ichikawa, S.; Matsuda, A.

    Tetrahedron 2005, 61, 5837-5842. DOI: 10.1016/j.tet.2005.04.019

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