Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Takehiro, Yamagishi"'
Publikováno v:
Chemistry Letters; Jan2024, Vol. 53 Issue 1, p1-4, 4p
Autor:
Xinyuan Cao, Narui Asano, Takehiro Yamagishi, Kyohei Yamaguchi, Norifumi Mizushima, Takahiro Noyori, Jin Kusaka, Kunitomo Minamitani, Yasuhiro Kondo
Publikováno v:
SAE Technical Paper Series.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::472878769dda745d7131882dd221ab59
https://doi.org/10.4271/2022-01-0655
https://doi.org/10.4271/2022-01-0655
Autor:
Ratnak Sok, Norifumi Mizushima, Takehiro Yamagishi, Takahiro Noyori, Toshinori Okajima, Makoto Nagata, Hajime Shingyouchi, Kyohei Yamaguchi, Jin Kusaka
Publikováno v:
SAE Technical Paper Series.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc54b452090d9b018578e67d48e8e7b9
https://doi.org/10.4271/2021-01-1244
https://doi.org/10.4271/2021-01-1244
Publikováno v:
Tetrahedron. 74:7068-7073
A method for the catalytic hydrophosphinylation of internal ynamides with H-phosphinates has been developed for the first time. The protocol employing the catalyst generated from NiBr2 and PPh3 could be applied to several types of ynamides and H-phos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7062569dd95b11435503bdec0be36bcd
https://doi.org/10.1016/j.tet.2018.10.042
https://doi.org/10.1016/j.tet.2018.10.042
Publikováno v:
Tetrahedron. 73:1705-1710
A method for Cu(OAc)2-catalyzed hydrophosphinylation of ynamides was developed and applied to several types of terminal ynamides and H-phosphinates. The products were transformed into β-aminophosphinates, which are useful for the preparation of biol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0fd5ae8efb78d9e26e79f65545a78a0b
https://doi.org/10.1016/j.tet.2017.02.010
https://doi.org/10.1016/j.tet.2017.02.010
Publikováno v:
Tetrahedron. 71:7614-7619
Synthesis of aryl phosphinates was achieved through cross-coupling reactions of aryl iodides with H -phosphinates catalyzed by nickel under mild conditions. The method was applicable to various aryl iodides and H -phosphinates having defined stereoch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53ea114f2bcd8b4dfb3f73d3ad80adae
https://doi.org/10.1016/j.tet.2015.07.073
https://doi.org/10.1016/j.tet.2015.07.073
Autor:
Takehiro Yamagishi
Publikováno v:
YAKUGAKU ZASSHI. 134:915-924
Phosphinyl dipeptide isosteres (PDIs) are important compounds for the development of potent and selective inhibitors of various aspartic proteases and Zn metalloproteases. The stereochemistry of PDIs affects their biological activity. PDIs were prepa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ed9a558502174e3087fb832d8e9ba69
https://doi.org/10.1248/yakushi.14-00157
https://doi.org/10.1248/yakushi.14-00157
Autor:
Yasushi Kawase, Teruo Kutsuma, Jun-ya Kato, Takeo Iwakuma, Tadashi Kataoka, Takehiro Yamagishi, Tsutomu Yokomatsu
Publikováno v:
Synthesis. 46:455-464
An efficient method for the direct reductive alkylation of hydrazine derivatives with α-picoline-borane has been developed to synthesize a variety of N-alkylhydrazine derivatives. This method provided N,N-dialkylhydrazine derivatives and N-monoalkyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5358a824cb98685ec72eea61af20477a
https://doi.org/10.1055/s-0033-1340484
https://doi.org/10.1055/s-0033-1340484
Clarithromycin Attenuates the Bronchial Epithelial Damage Induced by Mycoplasma pneumoniae Infection
Autor:
Takehiro Yamagishi, Hisato Sadakata, Tsutomu Tomita, Tae Nagami, Hiroshi Tanaka, Shun Miyazaki, Shuhei Shirata
Publikováno v:
Advances in Microbiology. :697-703
To analyze the bronchial epithelial cell damage induced by Mycoplasma pneumonia and the therapeutic effects of clarithromycin, we observed bronchial tissue damage by using a mouse model and performing immunostaining and scanning electron microscopy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa5ed71430ef760b83362485c56e8696
https://doi.org/10.4236/aim.2014.411075
https://doi.org/10.4236/aim.2014.411075
Publikováno v:
Synlett. 24:1998-2002
We achieved the first total synthesis of (±)-incargutines A and B, which were isolated from the roots of Incarvillea arguta, utilizing In(OTf)3-catalyzed enolization of cyclohexenone derivatives subsequent to an intramolecular Alder–Rickert reacti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f6d6a94e70094d85ca07c19de040b77
https://doi.org/10.1055/s-0033-1339484
https://doi.org/10.1055/s-0033-1339484