Y. Nishimura

(3R)-3-amino-4-(2,4,5-trifluorophenyl)-N-{4-[6-(2-methoxyethoxy)benzothiazol-2-yl]tetrahydropyran-4-yl}butanamide as a potent dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes.

H. Kozono, H. Fujii, Mikiya Satoh, 2008, Bioorganic & medicinal chemistry letters.

Discovery of 1-oxa-4,9-diazaspiro[5.5]undecane-based trisubstituted urea derivatives as highly potent soluble epoxide hydrolase inhibitors and orally active drug candidates for treating of chronic kidney diseases.

M. Yamada, Y. Kato, H. Kigoshi, 2014, Bioorganic & medicinal chemistry letters.

Discovery of 2,8-diazaspiro[4.5]decane-based trisubstituted urea derivatives as highly potent soluble epoxide hydrolase inhibitors and orally active drug candidates for treating hypertension.

M. Yamada, Y. Kato, Takumi Aoki, 2013, Bioorganic & medicinal chemistry letters.

Concise Synthesis of(±)-Brevioxime

T. Kitahara, Y. Nishimura, 2000 .

A New Synthesis of (−)‐Frontalin, the Bark Beetle Pheromone

K. Mori, Y. Nishimura, 1998 .

Sterols of Cajanus cajan and three other leguminosae seeds

Naomi Nakamura, P. Ghosh, T. Akihisa, 1992 .

Sterols of three leguminosae seeds: occurrence of 24α-ethyl-5α-cholest-9(11)-en-3β-ol and both c-24 epimers of 24-ethylcholesta-5,25-dien-3β-ol

P. Ghosh, T. Akihisa, T. Tamura, 1991 .

Pheromone Synthesis, CLXXVIII. – Synthesis of (−)‐exo‐Isobrevicomin and Its (−)‐endo Isomer, the Components of The Male‐Produced Volatiles of the Mountain Pine Beetle, Dendroctonus ponderosae

K. Mori, H. Takikawa, Y. Nishimura, 1997 .