Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Katsutoshi Aono"'
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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The genome sequences of unicellular holozoans, the closest relatives to animals, are shedding light on the evolution of animal multicellularity, shaping the genetic contents of the putative premetazoans. However, the assembly quality of the genomes r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87b9476e648b585fac9051a86e3d0480
http://hdl.handle.net/10261/206216
http://hdl.handle.net/10261/206216
Publikováno v:
Chemistry Letters. 15:429-432
Glycolatoplatinum(II) complexes, [Pt(OCOCH2O)L2], having a novel five-membered ring structure were obtained by adding an equimolar quantity of glycolic acid to cis-[Pt(OH)2L2] (L: NH3, amines) in water followed by heating. These complexes have also b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01da7629aeb7e0d911925f449db812e6
https://doi.org/10.1246/cl.1986.429
https://doi.org/10.1246/cl.1986.429
Autor:
Tetsushi Totani, Katsutoshi Aono
Publikováno v:
J. Chem. Soc., Dalton Trans.. :1190-1195
1-Amino-1,2-dicarbadodecaborane anions, o-RCB10H10CNH22–(R = H, Me, or Ph), are oxidized by K[MnO4] in liquid NH3 to give 1,1′-azo-o-carbaboranes, RCB10H10CNNCB10H10CR (3), whereas oxidation of HCB10H10CCB10H10CNH24– in the same solvent exclusi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::224e6014fa959c29c77cc5897b879046
https://doi.org/10.1039/dt9810001190
https://doi.org/10.1039/dt9810001190
Publikováno v:
Chemical and Pharmaceutical Bulletin. 15:329-336
Proton magnetic resonance spectra of substituted ammonium ions were studied in deuterium oxide, being classified in methylammonium, ethylammonium, β-substituted ethylammonium, and vinylammonium ions. The chemical shifts of the methyl groups are disc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d549d883a85d6a18d1acb999b11ead66
https://doi.org/10.1248/cpb.15.329
https://doi.org/10.1248/cpb.15.329
Publikováno v:
Canadian Journal of Chemistry. 45:1185-1193
The substituent effects on the chemical shifts of the C9 bridge protons in a series of 6-substituted benzonorbornenes and benzonorbornadienes, and on those of the C2 protons in 5-substituted 2-indanols, were investigated. They were linearly correlate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c216a065770bb8df3598ecd99bc3307a
https://doi.org/10.1139/v67-197
https://doi.org/10.1139/v67-197
Publikováno v:
Journal of the American Chemical Society. 89:2765-2767
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa9a82494d9298007ffde84ef3b504b3
https://doi.org/10.1021/ja00987a064
https://doi.org/10.1021/ja00987a064
Autor:
Katsutoshi Aono, Tetsushi Totani
Publikováno v:
Chemischer Informationsdienst. 12
1-Amino-1,2-dicarbadodecaborane anions, o-RCB10H10CNH22–(R = H, Me, or Ph), are oxidized by K[MnO4] in liquid NH3 to give 1,1′-azo-o-carbaboranes, RCB10H10CNNCB10H10CR (3), whereas oxidation of HCB10H10CCB10H10CNH24– in the same solvent exclusi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90adbf538e6ce3763548e5764b1d54fb
https://doi.org/10.1002/chin.198130263
https://doi.org/10.1002/chin.198130263
Autor:
Toshio Nakagawa, Katsutoshi Aono
Publikováno v:
Chemicalpharmaceutical bulletin. 24(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3c802aef578b6a3777fd141867259bf
https://pubmed.ncbi.nlm.nih.gov/949818
https://pubmed.ncbi.nlm.nih.gov/949818
Publikováno v:
Journal of medicinal chemistry. 24(12)
Various o-carboranes and nido-type dicarbollide anions have been synthesized and tested for antimicrobial activity. Nearly all of the dicarbollide monoanions investigated were active in vitro against fungi such as Candida albicans, Aspergillus fumiga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa34c6854e31099a50e378e6f3b4adef
https://pubmed.ncbi.nlm.nih.gov/7310826
https://pubmed.ncbi.nlm.nih.gov/7310826
Publikováno v:
Chemischer Informationsdienst. 13
Various o-carboranes and nido-type dicarbollide anions have been synthesized and tested for antimicrobial activity. Nearly all of the dicarbollide monoanions investigated were active in vitro against fungi such as Candida albicans, Aspergillus fumiga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::861ad45c2c39115afabd0f4a46016f60
https://doi.org/10.1002/chin.198222268
https://doi.org/10.1002/chin.198222268