S. Shibuya

Synthesis and evaluation of a difluoromethylene analogue of sphingomyelin as an inhibitor of sphingomyelinase.

S. Soeda, H. Shimeno, T. Yokomatsu, 2001, Bioorganic & medicinal chemistry letters.

Synthesis and evaluation of multisubstrate analogue inhibitors of purine nucleoside phosphorylases.

Y. Hayakawa, S. Koyanagi, S. Soeda, 2000, Bioorganic & medicinal chemistry.

Synthesis and biological evaluation of 1,1-difluoro-2-(tetrahydro-3-furanyl)ethylphosphonic acids possessing a N9-purinylmethyl functional group at the ring. a new class of inhibitors for purine nucleoside phosphorylases.

Y. Hayakawa, S. Soeda, H. Shimeno, 1999, Bioorganic & medicinal chemistry letters.

Synthesis of 1,1-difluoro-5-(1H-9-purinyl)-2-pentenylphosphonic acids and the related methano analogues. Remarkable effect of the nucleobases and the cyclopropane rings on inhibitory activity toward purine nucleoside phosphorylase.

H. Abe, M. Sato, S. Soeda, 1998, Bioorganic & medicinal chemistry.

Diels-Alder cycloaddition of novel buta-1,-3-diene derivatives possessing a (diethoxyphosphinoyl)difluoromethyl unit.

T. Yokomatsu, S. Shibuya, S. Katayama, 2001, Chemical communications.

Synthesis of isoquinolines. XI. Dibenzo[c,f]-1-azabicyclo[3.3.1]nonanes and 4-phenyl-1,2,3,4-tetrahydroisoquinolines

J. Bobbitt, S. Shibuya, 1970 .

A new route to chiral pyrrolidines via radical cyclisation; enantioselective synthesis of (+)-bulgecinine

Y. Yuasa, J. Ando, S. Shibuya, 1994 .