Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Yuzuru Sanemitsu"'
Autor:
Yuzuru Sanemitsu, Shinichi Kawamura
Publikováno v:
Journal of Pesticide Science. 33:181-189
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8df7aa61639e9610f61e565af923818
https://doi.org/10.1584/jpestics.33.181
https://doi.org/10.1584/jpestics.33.181
Publikováno v:
Journal of Pesticide Science. 31:305-310
A novel series of substituted 2-acylimino-1,3-thiazolines was synthesized and their herbicidal activity against upland weeds and selectivity against crops was assessed. The structure–activity relationships were probed by substitution of the thiazol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e72c3ba4c9aece154d775de2fb49949
https://doi.org/10.1584/jpestics.31.305
https://doi.org/10.1584/jpestics.31.305
Autor:
Yuzuru Sanemitsu
Publikováno v:
Journal of Pesticide Science. 30:165-170
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7066e125511602a010851c8699f163e6
https://doi.org/10.1584/jpestics.30.165
https://doi.org/10.1584/jpestics.30.165
Autor:
Shinichi Kawamura, Yuzuru Sanemitsu
Publikováno v:
Journal of Pesticide Science. 33:175-177
Various heterocyclic compounds have significantly contributed to current commercial agrochemicals. We focused our attention on these heterocycles as screening targets to create novel bioactive compounds. Although recent progress in agrochemical resea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d91399d695ad377746f63301ef30d207
https://doi.org/10.1584/jpestics.j08-02
https://doi.org/10.1584/jpestics.j08-02
Autor:
Noriko Osawa, Shoetsu Konno, Hiroshi Yamanaka, Masaharu Sakaki, Yuzuru Sanemitsu, Shinichi Kawamura
Publikováno v:
Journal of Agricultural and Food Chemistry. 43:838-842
A variety of 6-substituted 3,5-diaryl-1,2,4-triazines were synthesized. These diaryltriazines, which incorporate a triazine nucleus substituted by two aryl moieties, comprise a new class of bleaching herbicides. The structure-activity relationships w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23b67c20ef435dc26bae0b1ae38edc9a
https://doi.org/10.1021/jf00051a053
https://doi.org/10.1021/jf00051a053
Publikováno v:
Journal of Agricultural and Food Chemistry. 41:288-291
A novel series of substituted 2,4-diarylpyrimidines was synthesized and found to possess bleaching herbicidal activity. These diarylpyrimidines, which incorporate a pyrimidine nucleus substituted by two aryl moieties, are new chemical families of ble
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb54828d5930ff6915222589c14a0290
https://doi.org/10.1021/jf00026a030
https://doi.org/10.1021/jf00026a030
Publikováno v:
Pesticide Science. 39:169-177
The relationship between the hydrophobicity of certain herbicidal compounds and the bleaching pattern caused on radish cotyledons was investigated. Seed treatment with diphenylpyridones, as well as with established herbicides, produced three types of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52f58a4279608dfe1876dbc83fa9120a
https://doi.org/10.1002/ps.2780390302
https://doi.org/10.1002/ps.2780390302
Autor:
Shinichi Kawamura, Yuzuru Sanemitsu
Publikováno v:
The Journal of Organic Chemistry. 58:414-418
Azetidinones or oxazinones, being easily prepared from enamines and acyl isocyanates, were transformed into highly substituted 4(3H)-pyrimidinones upon treatment with ammonium acetate. This novel ring transformation was also accomplished through a on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e350b45788f43cb2c233eed7a04ff64
https://doi.org/10.1021/jo00054a026
https://doi.org/10.1021/jo00054a026
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdf5b4206bc8a38846ca7b9530b23fa3
https://doi.org/10.1002/chin.199102239
https://doi.org/10.1002/chin.199102239
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6765afc6f0ec2b945aaf6df804ec7b5d
https://doi.org/10.1002/chin.199149163
https://doi.org/10.1002/chin.199149163