S. Kodato

发表

Probes for narcotic receptor mediated phenomena. 37. Synthesis and opioid binding affinity of the final pair of oxide-bridged phenylmorphans, the ortho- and para-b-isomers and their N-phenethyl analogues, and the synthesis of the N-phenethyl analogues of the ortho- and para-d-isomers.

J. Deschamps, K. Rice, R. Rothman, 2008, Journal of medicinal chemistry.

Antiulcer activity of dehydroabietic acid derivatives.

H. Tamaki, S. Kodato, H. Nakai, 1985, Chemical & pharmaceutical bulletin.

ANTIULCER ACTIVITY OF DEHYDROABIETIC ACID DERIVATIVES

H. Tamaki, S. Kodato, H. Nakai, 1985 .

Probes for narcotic receptor-mediated phenomena. 33. Construction of a strained trans-5,6-ring system by displacement of a nitro-activated aromatic fluorine. synthesis of the penultimate oxide-bridged phenylmorphans.

J. Deschamps, C. George, J. Flippen-Anderson, 2004, The Journal of organic chemistry.

Oxidative dimerization of Nb-acyltryptophans total synthesis and absolute configuration of ditryptophenaline

H. Sugumi, T. Hino, M. Nakagawa, 1981 .

Total synthesis of (+)-fumitremorgin B, its epimeric isomers, and demethoxy derivatives

T. Hino, M. Nakagawa, T. Kawate, 1988 .

Oxidative dimerization of Nb-methoxycarbonyltryptamines by dye-sensitized photooxygenation in formic acid. Synthesis of (±)-folicanthine and (±)-chimonanthine

T. Hino, M. Nakagawa, S. Kodato, 1978 .

Total synthesis of fumitremorgin B

T. Hino, M. Nakagawa, T. Kawate, 1986 .

Synthesis of cerebroside B1b with antiulcerogenic activity II. Total synthesis and determination of absolute configuration of cerebroside B1b and its stereoisomers

T. Hino, M. Nakagawa, S. Kodato, 1989 .

Synthesis of cerebroside B1b with antiulcerogenic activity I. Synthesis of ceramides with optically active α-hydroxypalmitic acids.

K. Nakayama, T. Hino, M. Nakagawa, 1989 .

Total synthesis and determination of absolute configuration of cerebroside B1b and its stereoisomers

K. Nakayama, T. Hino, M. Nakagawa, 1987 .

Synthesis of rac-(1R,4aR,9aR)-2-methyl-1,3,4,9a-tetrahydro-2H-1,4a-propanobenzofuro[2,3-c]pyridin-6-ol. An unusual double rearrangement leading to the ortho- and para-f oxide-bridged phenylmorphan isomers.

J. Deschamps, J. Flippen-Anderson, J. Linders, 2004, Organic & biomolecular chemistry.

Dye-sensitized Photooxygenation of Tyrptophan : 3a-Hydroperoxypyrroloindole as a Labile Precursor of Formylkynurenine

S. Kato, B. Witkop, Hideyuki Watanabe, 1981 .

Synthesis of novel pyridotriazepinones as antisecretory agents.

Y. Nishibata, H. Tamaki, S. Kodato, 1987, Chemical & pharmaceutical bulletin.

Synthetic Approaches to Fumitremorgins. III. : Synthesis of Optically Active Pentacyclic Ring Systems, and Their Oxidation at Ring C

H. Fukushima, T. Hino, M. Nakagawa, 1989 .

Synthetic approach to the total synthesis of fumitremorgins II synthesis of optically active pentacyclic intermediates and their dehydrogenation

H. Fukushima, T. Hino, M. Nakagawa, 1986 .

A valid model for the mechanism of oxidation of tryptophan to formylkynurenine-25 years later.

B. Witkop, J. Flippen, Hideyuki Watanabe, 1977, Proceedings of the National Academy of Sciences of the United States of America.