Y. Kawanaka

发表

Design and synthesis of orally bioavailable inhibitors of inducible nitric oxide synthase. Part 1: synthesis and biological evaluation of dihydropyridin-2-imines.

S. Kusuda, K. Hirai, M. Toda, 2002, Bioorganic & medicinal chemistry letters.

Design and synthesis of orally bioavailable inhibitors of inducible nitric oxide synthase. synthesis and biological evaluation of dihydropyridin-2(1H)-imines and 1,5,6,7-tetrahydro-2H-azepin-2-imines.

S. Kusuda, K. Hirai, M. Toda, 2003, Bioorganic & medicinal chemistry.

Allyl as Protective Group for the Acidic Hydrogen of Malonic Ester

F. Sato, T. Yamazaki, Y. Kawanaka, 1996 .

Design and synthesis of orally bioavailable inhibitors of inducible nitric oxide synthase. Identification of 2-azabicyclo[4.1.0]heptan-3-imines.

S. Kusuda, K. Hirai, M. Toda, 2003, Bioorganic & medicinal chemistry.

Design and synthesis of inhibitors of inducible nitric oxide synthase. Discovery of a new chemical lead with potential for oral bioavailability.

S. Kusuda, K. Hirai, M. Toda, 2003, European journal of medicinal chemistry.

SYNTHESIS OF CHIRAL ALLYLTITANIUMS HAVING AN AMINO GROUP AT THE C-4 POSITION AND THEIR DIASTEREOSELECTIVE ADDITION REACTION WITH ALDEHYDES

X. Teng, S. Okamoto, F. Sato, 1997 .

An improved synthesis of the selective EP4 receptor agonist ONO-4819.

H. Araki, T. Shiraishi, Chisa Ohta, 2009, The Journal of organic chemistry.

N-heterocyclic carbene-catalyzed enantioselective Mannich reactions with alpha-aryloxyacetaldehydes.

K. Scheidt, E. Phillips, Y. Kawanaka, 2009, Journal of the American Chemical Society.

A new process for synthesis of the astrocyte activation suppressor, ONO-2506

Y. Hamada, M. Okamoto, Kazuhiro Nakabayashi, 2005 .

Process development of ONO-2506: A therapeutic agent for stroke and Alzheimer's disease

S. Hashimoto, M. Okamoto, T. Hasegawa, 2003 .

Synthesis of the key component for preparation of 6-ketoprostaglandins by a two-component coupling process: synthesis of 6-keto-prostaglandin E1, ornoprostil and Δ2-trans-6-ketoprostaglandin E1

S. Okamoto, N. Ono, F. Sato, 1996 .

Synthesis of a key intermediate for preparation of 4,5-didehydro prostaglandins containing an allenyl side-chain group via two-component coupling process. Synthesis of enprostil

N. Ono, F. Sato, Y. Kawanaka, 1994 .

Mitochondrial alcohol dehydrogenase from ethanol-grown Euglena gracilis.

H. Inui, Y. Nakano, K. Miyatake, 1995, Journal of biochemistry.

Design and synthesis of a selective EP4-receptor agonist. Part 4: practical synthesis and biological evaluation of a novel highly selective EP4-receptor agonist.

M. Toda, T. Shiraishi, Y. Shinagawa, 2002, Bioorganic & medicinal chemistry.

N-heterocyclic carbene-catalyzed enantioselective Mannich reactions with alpha-aryloxyacetaldehydes.

K. Scheidt, E. Phillips, Y. Kawanaka, 2009, Journal of the American Chemical Society.