T. Nakae

Syntheses of pseudo-.ALPHA.-D-glucopyranose and pseudo-.BETA.-L-idopyranose, two optically active pseudo-hexopyranoses, from D-glucose by using stereoselective reductive deacetoxylation with sodium borohydride and cyclitol formation from nitrofuranose as key reactions.

I. Kitagawa, M. Yoshikawa, B. Cha, 1988 .

Synthesis of structural analogues of leukotriene B4 and their receptor binding activity.

H. Nakai, N. Hamanaka, M. Nishizaki, 1997, Bioorganic & medicinal chemistry.

A NEW APPROACH TO THE SYNTHESIS OF OPTICALLY ACTIVE CYCLOHEXANE ANALOGS OF NUCLEOSIDE USING A MICHAEL-TYPE ADDITION REACTION TO NITRO-CYCLOHEXENES AS A KEY REACTION

I. Kitagawa, M. Yoshikawa, Y. Takinami, 1989 .

Synthesis and structure-activity relationships of a series of substituted-phenylpropionic acids as a novel class of leukotriene B4 antagonists.

N. Hamanaka, A. Kawasaki, T. Miyamoto, 1991, Advances in prostaglandin, thromboxane, and leukotriene research.