S. Kuroda

发表

Design, synthesis, and structure-activity relationships of potent GPIIb/IIIa antagonists: discovery of FK419.

T. Aoki, J. Seki, M. Ohkubo, 2005, Bioorganic & medicinal chemistry.

Novel adenosine A1 receptor antagonists. Synthesis and structure-activity relationships of a novel series of 3-(2-cyclohexenyl-3-oxo-2,3-dihydropyridazin-6-yl)-2-phenylpyrazolo[1,5 -a]pyridines.

Y. Tenda, K. Durkin, H. Itani, 2000, Bioorganic & medicinal chemistry.

Design, synthesis and biological evaluation of a novel series of potent, orally active adenosine A1 receptor antagonists with high blood-brain barrier permeability.

Y. Tenda, Y. Tomishima, F. Takamura, 2001, Chemical & pharmaceutical bulletin.

Stereoselective Synthesis of (±)-Ireland Alcohol Using Titanium-Mediated [2,3]Wittig Rearrangement Product as a Starting Material

T. Katsuki, H. Okamura, M. Yamaguchi, 1992 .

Synthesis and biological evaluation of novel 2-vinyl carbapenems. Remarkable DHP-1 stability of 1′-substituted analogs

T. Kamimura, K. Hattori, T. Chiba, 1996 .

Synthesis and antibacterial activity of novel 4-pyrrolidinylthio carbapenems--I. 2-Alkoxymethyl derivatives.

M. Murata, T. Kamimura, H. Azami, 1997, Bioorganic & medicinal chemistry.

A formal synthesis of aplysiatoxin: enantioselective synthesis of kishi's aldehyde

T. Katsuki, H. Okamura, M. Yamaguchi, 1993 .

Synthesis of aplysiatoxin: stereoselective synthesis of key fragments

T. Katsuki, H. Okamura, M. Yamaguchi, 1991 .

Stereoselectivity in [2,3]wittig rearrangement of isopropyl [(2E)-1 -(ω-benzyloxyalkyl)-2-butenyl]oxyacetate. Preparation of potent building blocks for the synthesis of polyoxo compounds

T. Hanamoto, T. Katsuki, S. Kuroda, 1988 .

Stereoselective synthesis of (2,4)-dien-1-ols; key intermidiates for synthesis of sex pheromones of silk worm and of grape vine moth

T. Katsuki, M. Yamaguchi, S. Kuroda, 1987 .

Synthesis and antibacterial activity of novel 4-pyrrolidinylthio carbapenems. Part III:

M. Sakurai, T. Kamimura, K. Washizuka, 1999 .

Synthesis of the water-soluble adenosine A1 receptor antagonist FR166124 through a novel sequential Horner-Emmons / isomerization reaction

T. Kinoshita, I. Nakanishi, K. Durkin, 1999 .

Discovery of FR166124, a novel water-soluble pyrazolo-[1,5-a]pyridine adenosine A1 receptor antagonist.

T. Kinoshita, Y. Tenda, K. Durkin, 1999, Bioorganic & medicinal chemistry letters.

Pharmacological characterization of FR194921, a new potent, selective, and orally active antagonist for central adenosine A1 receptors.

A. Iwashita, T. Yamaji, T. Mihara, 2004, Journal of pharmacological sciences.

A formal total synthesis of aplysiatoxin

T. Katsuki, H. Okamura, M. Yamaguchi, 1991 .