Takahiko Nakae

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.

Isao Kitagawa, Bae Cheon, Takahiko Nakae et al. · Chemical and Pharmaceutical Bulletin · 1989 · 27 citations · Full text

Bioorganic Chemistry, Derivatives, Biochemistry +14

Syntheses of (+)-cyclaradine and (+)-9-pseudo-.BETA.-L-xylofuranosyladenine, two optically active cyclopentane analogs of nucleoside.

Masayuki Yoshikawa, Takahiko Nakae, Bae Cheon et al. · Chemical and Pharmaceutical Bulletin · 1989 · 26 citations · Full text

Active Cyclopentane Analogs, Bioorganic Chemistry, Engineering +10

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.

Masayuki Yoshikawa, Bae Cheon, Takahiko Nakae et al. · Chemical and Pharmaceutical Bulletin · 1988 · 14 citations · Full text

Bioorganic Chemistry, Engineering, Glycobiology +16

Intramolecular carbonyl-mediated electrochemical oxidation: Skeletal rearrangement of an oleanene triterpene and its oligoside

Masayuki Yoshikawa, Nobutoshi Murakami, TOSHIO TANIYAMA et al. · Tetrahedron Letters · 1987 · 10 citations

Engineering, Skeletal Rearrangement, Biochemistry +9