Kiyoshi Ikeda
Department of Organic Chemistry
School of Pharmaceutical Sciences
University of Shizuoka
52-1 Yada
Japan
[email]@ys2.u-shizuoka-ken.ac.jp
Name/email consistency: high
- 2-Deoxy-2,3-didehydro-N-acetylneuraminic acid analogs structurally modified by thiocarbamoylalkyl groups at the C-4 position: Synthesis and biological evaluation as inhibitors of human parainfluenza virus type 1. Ikeda, K., Sato, K., Nishino, R., Aoyama, S., Suzuki, T., Sato, M. Bioorg. Med. Chem. (2008)
- Novel glycosylation reactions using glycosyl thioimidates of N-acetylneuraminic acid as sialyl donors. Ikeda, K., Aizawa, M., Sato, K., Sato, M. Bioorg. Med. Chem. Lett. (2006)
- Preparation of a fluorous protecting group and its application to the chemoenzymatic synthesis of sialidase inhibitor. Ikeda, K., Mori, H., Sato, M. Chem. Commun. (Camb.) (2006)
- 2-Deoxy-2,3-didehydro-N-acetylneuraminic acid analogues structurally modified at the C-4 position: synthesis and biological evaluation as inhibitors of human parainfluenza virus type 1. Ikeda, K., Sato, K., Kitani, S., Suzuki, T., Maki, N., Suzuki, Y., Sato, M. Bioorg. Med. Chem. (2006)
- 2beta,3beta-Difluorosialic acid derivatives structurally modified at the C-4 position: synthesis and biological evaluation as inhibitors of human parainfluenza virus type 1. Ikeda, K., Kitani, S., Sato, K., Suzuki, T., Hosokawa, C., Suzuki, Y., Tanaka, K., Sato, M. Carbohydr. Res. (2004)
- Glycosylation of sialyl acetates with a novel catalyst combination: bismuth triflate and BF3.OEt2 system. Ikeda, K., Torisawa, Y., Nishi, T., Minamikawa, J., Tanaka, K., Sato, M. Bioorg. Med. Chem. (2003)
- Use of phenyl 2-alpha-selenoglycosides of N-acetylneuraminic acid as a glycosyl donor for the glycosylation reactions. Ikeda, K., Sugiyama, Y., Tanaka, K., Sato, M. Bioorg. Med. Chem. Lett. (2002)
- Synthesis of 2-deoxy-2,3-didehydro-N-acetylneuraminic acid analogues modified at the C-4 and C-9 positions and their behaviour towards sialidase from influenza virus and pig liver membrane. Ikeda, K., Sano, K., Ito, M., Saito, M., Hidari, K., Suzuki, T., Suzuki, Y., Tanaka, K. Carbohydr. Res. (2001)
- Inhibition of HIV-1 infection by synthetic peptide analogues derived from the NH(2)-Terminal extracellular region of GPR1. Ikeda, K., Konishi, K., Sato, M., Hoshino, H., Tanaka, K. Bioorg. Med. Chem. Lett. (2001)
