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: Yamano, T Kikumoto, F Yamamoto, S Miwa, K Kawada, M Ito, T Ikemoto, T Tomimatsu, K Mizuno, Y

Citation: T. Yamano et al., A practical method for optical resolution of racemic alcohols or esters via lipase-catalyzed transformation and sulfation, CHEM LETT, (5), 2000, pp. 448-449

Authors: Kawamoto, T Tomimatsu, K Ikemoto, T Abe, H Hamamura, K Takatani, M

Citation: T. Kawamoto et al., Efficient syntheses of a novel 5-thia-1-azacycl[3.3.2]azine ring system and 3H-1,4-diazacycl[3.3.2]azine derivatives, TETRAHEDR L, 41(18), 2000, pp. 3447-3451

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