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Citation: O. Nishimura et al., Bio-organic synthesis of a newly isolated peptide metastin, metastasis suppressor gene KiSS-1 processing product, J CHEM S P1, (15), 2001, pp. 1748-1750

Authors: Ikemoto, T Wakimasu, M

Citation: T. Ikemoto et M. Wakimasu, Reactions with N-chlorosuccinimide of various methylimidazo[1, 2-a]pyridine derivatives with electron-withdrawing group substituted at the 3-position, HETEROCYCLE, 55(1), 2001, pp. 99-108

Authors: Ikemoto, T Nishiguchi, A Mitsudera, H Wakimasu, M Tomimatsu, K

Citation: T. Ikemoto et al., Convenient efficient synthesis of TAK-779, a nonpeptide CCR5 antagonist: development of preparation of various ammonium salts using trialkylphosphiteand N-halogenosuccinimide, TETRAHEDRON, 57(8), 2001, pp. 1525-1529

Authors: Ikemoto, T Ito, T Hashimoto, H Kawarasaki, T Nishiguchi, A Mitsudera, H Wakimasu, M Tomimatsu, K

Citation: T. Ikemoto et al., Development of a new synthetic route of a non-peptide CCR5 antagonist, TAK-779, for large-scale preparation, ORG PROC R, 4(6), 2000, pp. 520-525

Authors: Ikemoto, T Kawamoto, T Tomimatsu, K Takatani, M Wakimasu, M

Citation: T. Ikemoto et al., A practical synthesis of the chronic renal disease agent, 4,5-dihydro-3H-1,4,8b-triazaacenaphthylen-3-one derivatives, using regioselective chlorination of ethyl 5-methylimidazo[1,2-a]pyridine-3-carboxy with N-chlorosuccinimide, TETRAHEDRON, 56(40), 2000, pp. 7915-7921