Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Honma Toyokuni"'
Autor:
Shigeru Mio, Hiromi Sano, Honma Toyokuni, Soji Sugai, Yuko Kumagawa, Masahiro Shindou, Junko Kitagawa
Publikováno v:
Bioscience, biotechnology, and biochemistry. 60(7)
We synthesized three hydantocidin derivatives and evaluated their herbicidal activity in order to elucidate the role of the spirohydantoin system at the anomeric center of hydantocidin. With application to foliage at 1000 ppm, only α-ureidoamide 14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::126a3db1264fac403ec58d42a9e098a2
https://pubmed.ncbi.nlm.nih.gov/27299724
https://pubmed.ncbi.nlm.nih.gov/27299724
Publikováno v:
Chemical and Pharmaceutical Bulletin. 48:509-515
4-Sulfenyl-2-carbamoyl-4-isoxazolin-3-ones (4) were designed on the basis of biological isosterism and prepared in four steps. Some of these compounds showed sufficient pre-emergent herbicidal activities against various kinds of weeds. Among the synt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ced1a72b83417e7c62df3eb4810ea171
https://doi.org/10.1248/cpb.48.509
https://doi.org/10.1248/cpb.48.509
Publikováno v:
Tetrahedron. 51:12563-12572
Synthesis of Spirothiohydantoin derivatives of hydantocidin is described. The key feature of the synthesis was Spirothiohydantoin ring formation through an iminophosphorane intermediate. Spirothiohydantoin derivative 2 maintained comparable herbicida
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::652e0e8d0541b71765581893670e05bd
https://doi.org/10.1016/0040-4020(95)00810-u
https://doi.org/10.1016/0040-4020(95)00810-u
Autor:
Junko Kitagawa, Masahiro Shindou, Shigeru Mio, Hiromi Sano, Honma Toyokuni, Masae Hamura, Soji Sugai
Publikováno v:
Bioscience, Biotechnology, and Biochemistry. 59:2247-2250
Syntheses of two carbonyl derivatives of hydantocidin 1, a potent, naturally occurring herbicide, and their herbicidal activity are described. Spiroimidazolidinone 2, the descarbonyl compound at C9, was prepared by employing reductive demethylsulfuri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7df5c985ffa18586a26f7c97984fcef
https://doi.org/10.1271/bbb.59.2247
https://doi.org/10.1271/bbb.59.2247
Publikováno v:
Agricultural and Biological Chemistry. 55:1105-1109
Syntheses of 2α-, 3- and 4-deoxy and 3,4-dideoxy derivatives of (+)-hydantocidin were accomplished by a single-electron-transfer reduction or by hydrogenation as the key step. The lack of herbicidal activity exhibited by these derivatives indicates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee4b16f6ede80c359d0170bae8eae2e2
https://doi.org/10.1080/00021369.1991.10870692
https://doi.org/10.1080/00021369.1991.10870692
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eca1be477e140edd813e9fe622076b8c
https://doi.org/10.1002/chin.200038132
https://doi.org/10.1002/chin.200038132
Publikováno v:
Agricultural and Biological Chemistry. 49:3563-3567
Many 1,2-benzisoxazole-3-acetamides were synthesized and their herbicidal activities in the paddy field were studied. Of the compounds tested, N-α,α-dimethylbenzyl-2-bromo-(1,2-benzisoxazol-3-yl)acetamide 10a was the most effective. Details of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff5a6d397beb5e4df2942bd383219523
https://doi.org/10.1271/bbb1961.49.3563
https://doi.org/10.1271/bbb1961.49.3563
Publikováno v:
ChemInform; Sep2000, Vol. 31 Issue 38, pno-no, 1p
Publikováno v:
In Tetrahedron 1995 51(46):12563-12572