Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Yuji Funaki"'
Publikováno v:
NIPPON KAGAKU KAISHI. :953-962
著者らが先に見出した殺菌剤ブチオオートの構造活性相関や作用機作研究の結果を活用した分子設計により,強い植物生畏調節活性と殺菌活性を餅せ持つ新規な2-(トリアゾリル)アリルア
Autor:
Hirotaka Takano, Kazuo Izumi, Masahiro Takahashi, Yuji Funaki, Masakazu Miyakado, Shizuya Tanaka
Publikováno v:
ACS Symposium Series ISBN: 9780841233218
Classical and Three-Dimensional QSAR in Agrochemistry
Classical and Three-Dimensional QSAR in Agrochemistry
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8286173b679b4355c5d580f7972d273
https://doi.org/10.1021/bk-1995-0606.ch008
https://doi.org/10.1021/bk-1995-0606.ch008
Publikováno v:
Agricultural and Biological Chemistry. 50:615-623
The title compounds were synthesized by employing 2-aminohexadecanoic acid and serine as the chiral sources, and served for an assay of fruiting-inducing activity on Schizophyllum commune. The structure-bioactivity relationship among closely related
Autor:
Yuji Funaki, Kenji Mori
Publikováno v:
Tetrahedron Letters. 25:5291-5294
A total synthesis of the natural enantiomer of the title compound was accomplished, which confirmed the structure proposed for the fruiting-inducing cerebroside of Schizophyllum commune .
Publikováno v:
The Journal of Organic Chemistry. 40:456-461
Publikováno v:
Journal of Pesticide Science. 9:229-236
4種のビニルトリアゾール系化合物, (Z)-および (E)-4,4-ジメチル-1-(置換フェニル)-2-(1,2,4-トリアゾール-1-イル)-1-ペンテン-3-オンとおのおののアルコール誘導体を合成し, その大麦うどんこ病
Publikováno v:
Bulletin of the Chemical Society of Japan. 48:1545-1548
The reduction of two dianhydroinositols: 1,2:3,4-dianhydro-5,6-O-cyclohexylidene-allo-inositol (1) and 1,2: 5,6-dianhydro-3,4-O-cyclohexylidene-allo-inositol (2), and four sulfonylated anhydroinositols: 1,2-anhydro-5,6-O-cyclohexylidene-3,4-di-O-mesy
Publikováno v:
Agricultural and Biological Chemistry. 50:615-623
The title compounds were synthesized by employing 2-aminohexadecanoic acid and serine as the chiral sources, and served for an assay of fruiting-inducing activity on Schizophyllum commune. The structure-bioactivity relationship among closely related
Autor:
Kenji Mori, Yuji Funaki
Publikováno v:
Tetrahedron. 41:2369-2377
A synthesis of the natural enantiomer as well as its diastereomer of the title compound was accomplished, confirming the structure proposed for the fruiting-inducing cerebroside of Schizophyllum commune .
Autor:
Yuji Funaki, Kenji Mori
Publikováno v:
Tetrahedron. 41:2379-2386
The title compound was synthesized by employing ( R )-2-aminohexadecanoic acid, D-glucose and ( S )-serine as the chiral sources, and the synthetic sample was found to be chemically and biologically identical with the fruiting-inducing cerebroside is