Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Kiyoharu Matsumoto"'
Autor:
Osamu Uchikawa, Toru Yamano, Kiyoharu Matsumoto, Mari Adachi, Kohji Fukatsu, Shigenori Ohkawa, Masayuki Yamashita, Mitsutaka Tanaka, Mitsuru Kawada
Publikováno v:
Tetrahedron: Asymmetry. 17:184-190
Asymmetric synthesis of a novel non-benzodiazepine hypnotic drug Ramelteon (TAK-375) was accomplished via asymmetric hydrogenation. Development of the substrate design revealed that a novel class of substrate, allylic acylamine 4a, was hydrogenated w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33a53d76d45e175c552445df77c641fd
https://doi.org/10.1016/j.tetasy.2005.11.005
https://doi.org/10.1016/j.tetasy.2005.11.005
Autor:
Shigenori Ohkawa, Takeshi Sakane, Osamu Uchikawa, Mitsuru Kawada, Yoichi Nagano, Naoki Tarui, Kiyoharu Matsumoto, Kazuo Nakahama
Publikováno v:
Journal of Bioscience and Bioengineering. 93:44-47
The chiral indan derivative (S)-2 (2-[(8S)-1,6,7,8-tetrahydro-2H-indeno[5,4-b]furan-8-yl]ethyl-amine) was synthesized by enzyme-catalyzed asymmetric hydrolysis of the racemic acetamide 1 (N-[2-(1,6,7,8-tetrahydro-2H-indeno[5,4-b]furan-8-yl)ethyl]acet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ddd428ec30181ca0421895217e0e968
https://doi.org/10.1016/s1389-1723(02)80052-4
https://doi.org/10.1016/s1389-1723(02)80052-4
Publikováno v:
Electrochemistry. 69:340-343
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb2ac99642446d3a7e451b72235614a3
https://doi.org/10.5796/electrochemistry.69.340
https://doi.org/10.5796/electrochemistry.69.340
Autor:
Shuji Fujioka, Yasunari Tohnai, Masanori Wada, Kiyoharu Matsumoto, Kazuhiro Nomura, Tatsuo Erabi
Publikováno v:
Bulletin of the Chemical Society of Japan. 72:2169-2175
The immobilization of reaction center complexes onto a gold electrode was attempted through the binding affinity between reaction centers and hydroquinone-2-thiol adsorbed on an electrode surface. The largest anodic photoresponse by immobilized react
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81eae941eacb1bd5f87495f18b96d0be
https://doi.org/10.1246/bcsj.72.2169
https://doi.org/10.1246/bcsj.72.2169
Autor:
Hideki Itoh, Shuichi Hayase, Noritaka Takahashi, Kiyoharu Matsumoto, Masanori Wada, Kazunori Fujimura, Tatsuo Erabi
Publikováno v:
Denki Kagaku oyobi Kogyo Butsuri Kagaku. 65:26-32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41aa6d3657b88938ca2dc81d6898677c
https://doi.org/10.5796/kogyobutsurikagaku.65.26
https://doi.org/10.5796/kogyobutsurikagaku.65.26
Autor:
Kiyoharu Matsumoto, Tsutomu Okamoto, Yukihiro Yokoyama, Tsuyoshi Ikeda, Masanori Wada, Megumi Moriuchi, Tatsuo Erabi, Shuichi Hayase
Publikováno v:
Bulletin of the Chemical Society of Japan. 68:1545-1550
An anodic photocurrent was generated when an SnO2 electrode, which was immersed in a culture medium of a photosynthetic bacterium, Rhodospirillum rubrum, or in a buffer suspending the cell body, was illuminated under potentiostatic conditions. The an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a76ac7c4f6f83c59baf97ea68b19b3a6
https://doi.org/10.1246/bcsj.68.1545
https://doi.org/10.1246/bcsj.68.1545
Autor:
Hidefumi Yukimasa, Masakuni Kori, Kazuo Nakahama, Kiyoharu Matsumoto, Yoichi Nagano, Toshiaki Nagata, Motowo Izawa, Takashi Miki, Naoki Tarui
Publikováno v:
ChemInform. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2ed4eb1863055bbf076508caa266353
https://doi.org/10.1002/chin.200229174
https://doi.org/10.1002/chin.200229174
Publikováno v:
Electrochemistry. 68:859-861
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6b00b08eee65b7126859d1b426e54ca
https://doi.org/10.5796/electrochemistry.68.859
https://doi.org/10.5796/electrochemistry.68.859
Publikováno v:
Denki Kagaku oyobi Kogyo Butsuri Kagaku. 65:673-675
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a142251ffe80c3bc876cd1132d349c77
https://doi.org/10.5796/kogyobutsurikagaku.65.673
https://doi.org/10.5796/kogyobutsurikagaku.65.673
Autor:
Yumi Imai, Ryosuke Tokunoh, Kohji Fukatsu, Keisuke Hirai, Shuji Hinuma, Shigenori Ohkawa, Masaomi Miyamoto, Osamu Uchikawa, Mitsuru Kawada, Koki Kato, Hisao Nishikawa, Kiyoharu Matsumoto
Publikováno v:
Journal of medicinal chemistry. 45(19)
To develop a new therapeutic agent for sleep disorders, we synthesized a novel series of tricyclic indan derivatives and evaluated them for their binding affinity to melatonin receptors. In our previous paper, we proposed a conformation of the methox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ef6846b06400a39831143572790ba58
https://pubmed.ncbi.nlm.nih.gov/12213063
https://pubmed.ncbi.nlm.nih.gov/12213063