Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Tadao Shoji"'
Publikováno v:
Journal of the Japan Society of Colour Material. 72:546-551
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6adedecef9924989dbae8c148454b0ea
https://doi.org/10.4011/shikizai1937.72.546
https://doi.org/10.4011/shikizai1937.72.546
Autor:
Naoki Yamamoto, Tadao Shoji, Toshiyuki Uryu, Kazuhiko Inazawa, Hideki Nakashima, Kaname Katsuraya
Publikováno v:
Macromolecules. 27:6695-6699
The synthesis of potently anti-HIV-active sulfated alkyl laminara-oligosaccharides composed of glucosidic residues of 5-9 was investigated. The anti-HIV activity and the anticoagulant activity of these sulfated alkyl laminara-oligosaccharides were as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99dcffdddee3c2ac5f71b016d84d012a
https://doi.org/10.1021/ma00101a001
https://doi.org/10.1021/ma00101a001
Autor:
Hideki Nakashima, Takashi Yoshida, Tadao Shoji, Naoya Ikushima, Nahoko Takahashi, Naoki Yamamoto, Toshiyuki Uryu, Kaname Katsuraya
Publikováno v:
Carbohydrate Research. 260:51-61
A series of sulfated alkyl oligosaccharides, including a sulfate dodecyl laminarapentaoside and a sulfated octadecyl maltohexaoside with potent anti-human immunodeficiency virus (HIV) activity, has been synthesized. An alkyl oligosaccharide in which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2ea8c848c605d259c098ce37b859e6e
https://doi.org/10.1016/0008-6215(94)80021-9
https://doi.org/10.1016/0008-6215(94)80021-9
Autor:
Nobuyuki Mori, Toshiyuki Matsuoka, Norio Minami, Isao Saito, Takashi Musha, Kazutoshi Miyake, Sachiyuki Hamano, Naoki Yoneda, Hiroki Ishihara, Masayuki Matsukura, Tadao Shoji, Osamu Hiroshima
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 4:213-218
A phenolic benzofuran derivative 1 was identified as an angiotensin II receptor antagonist by random screening. Structural modifications led to a novel series of N-(4-hydroxyphenylmethyl)benzimidazoles and imidazo[4,5-b]pyridines, some of which inhib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9beaa0c0a058b8bfb5bffbc35aaf4a6
https://doi.org/10.1016/s0960-894x(01)81149-5
https://doi.org/10.1016/s0960-894x(01)81149-5
Autor:
Ken-ichi Sato, Toru Fujisawa, Takeshi Hanamoto, Sadao Takehara, Takeshi Kuriyama, Nakamura Kayoko, Tadao Shoji, Tamejiro Hiyama, Masashi Osawa, Tetsuo Kusumoto
Publikováno v:
ChemInform. 22
The title ethers, expected chiral dopants for ferroelectric liquid crystals, were prepared by the allylation of chiral cyanohydrins under the acidic conditions followed by hydrogenation, or alternatively by the Johnson's cyanation of chiral acetals f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d73f72afc1d7d80cc2848c7930f59749
https://doi.org/10.1002/chin.199133147
https://doi.org/10.1002/chin.199133147
Autor:
Ken-ichi Sato, Sadao Takehara, Tamejiro Hiyama, Nakamura Kayoko, Takeshi Kuriyama, Masashi Osawa, Tetsuo Kusumoto, Nakayama Akiko, Tadao Shoji, Toru Fujisawa
Publikováno v:
ChemInform. 22
Optically active 2-alkyl-1-aryl-1-cyanocyclopropanes were synthesized from 2-aryl-4-hydroxyalkanenitriles which in turn were obtained by the reaction of chiral 1,2-epoxyalkanes with the carbanions derived from arylacetonitriles.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09d5e62218857e8fcbf9d490ed43f1de
https://doi.org/10.1002/chin.199151079
https://doi.org/10.1002/chin.199151079
Publikováno v:
ChemInform. 22
New chiral dopants having a chiral center directly connected to the core aromatic ring were designed and synthesized. Those discussed here are 1-arylethyl alkyl ethers, 2-arylpropanoates, O-acyl and O-alkylcyanohydrins, 2-arylalkanenitriles, aryl alk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49f4e20dc552f8c8d8baad3e08357929
https://doi.org/10.1002/chin.199151363
https://doi.org/10.1002/chin.199151363
Autor:
Masashi Osawa, Nakamura Kayoko, Tadao Shoji, Toru Fujisawa, Takeshi Hanamoto, Tetsuo Kusumoto, Tamejiro Hiyama, Takeshi Kuriyama, Sadao Takehara
Publikováno v:
ChemInform. 22
O-Acyl cyanohydrins having a chiral center directly connected to the core aromatic ring were prepared through asymmetric hydrocyanation of 4-substituted benzaldehydes and shown to be excellent chiral dopants for ferroelectric liquid crystals.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54092ad82ab15604987eea7f6b636459
https://doi.org/10.1002/chin.199146148
https://doi.org/10.1002/chin.199146148
Autor:
Masashi Osawa, Toru Fujisawa, Takeshi Kuriyama, Sadao Takehara, Nakamura Kayoko, Nakayama Akiko, Tamejiro Hiyama, Tadao Shoji, Tetsuo Kusumoto, Ken-ichi Sato, Kiyoharu Nishide
Publikováno v:
ChemInform. 22
Optically active α-aryl-γ-alkyl-γ-lactones were synthesized through the reaction of chiral 1,2-epoxyalkanes with the carbanion derived from 4-methoxyphenylacetonitrile or 4-methoxyphenylacetic acid and shown to be good chiral dopants for ferroelec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de62813efed145a5d62c4cd5271512d9
https://doi.org/10.1002/chin.199143122
https://doi.org/10.1002/chin.199143122
Autor:
Kazutoshi Miyake, Isao Saito, Toshiyuki Matsuoka, Norio Minami, Masayuki Matsukura, Tadao Shoji, Nobuyuki Mori, Naoki Yoneda, Sachiyuki Hamano, Osamu Hiroshima, Hiroki Ishihara, Takashi Musha
Publikováno v:
ChemInform. 25
A phenolic benzofuran derivative 1 was identified as an angiotensin II receptor antagonist by random screening. Structural modifications led to a novel series of N-(4-hydroxyphenylmethyl)benzimidazoles and imidazo[4,5-b]pyridines, some of which inhib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f424350e792c1fdd8966c9256139366
https://doi.org/10.1002/chin.199426186
https://doi.org/10.1002/chin.199426186