T. Imaoka

发表

Design and synthesis of 6-fluoro-2-naphthyl derivatives as novel CCR3 antagonists with reduced CYP2D6 inhibition.

M. Takeuchi, Keiko Suzuki, M. Ohta, 2008, Bioorganic & medicinal chemistry.

Synthesis, biological evaluation, and metabolic stability of acrylamide derivatives as novel CCR3 antagonists.

K. Ohno, M. Takeuchi, Keiko Suzuki, 2009, Bioorganic & medicinal chemistry.

Synthesis and structure-activity relationships of N-{1-[(6-fluoro-2-naphthyl)methyl]piperidin-4-yl}benzamide derivatives as novel CCR3 antagonists.

M. Takeuchi, Keiko Suzuki, M. Ohta, 2008, Bioorganic & medicinal chemistry.

Discovery and structure-activity relationships of urea derivatives as potent and novel CCR3 antagonists.

M. Takeuchi, M. Ohta, T. Morokata, 2012, Bioorganic & medicinal chemistry letters.

Stereoselective Construction of Functionalized Fusicoccane Framework

H. Okamoto, N. Kato, H. Takeshita, 1994 .

Stereoselective Construction of Functionalized Fusicoccane Framework.

H. Okamoto, N. Kato, H. Takeshita, 1994 .

A Photoallylation of N-Methylarenedicarboximides by Allylsilanes

T. Araki, T. Shiragami, Y. Kubo, 1986 .

Synthesis and Antitumor Activity of [3-Acetyl-2,4(3H,5H)-furandionato-O3,O4] [(1R,2R)-cyclohexanediamine]platinum(1+) Ion Complex and Its Derivatives

Y. Kitano, M. Mutoh, G. Hata, 1993 .

Corrigendum to “Synthesis and structure–activity relationships of N-{1-[(6-fluoro-2-naphthyl)methyl]piperidin-4-yl}benzamide derivatives as novel CCR3 antagonists” [Bioorg. Med. Chem. 16 (2008) 144–156]

M. Takeuchi, Keiko Suzuki, M. Ohta, 2008 .