Zobrazeno 1 - 10
of 2 391
pro vyhledávání: '"Yasuhiro Uozumi"'
Publikováno v:
ACS Omega, Vol 5, Iss 41, Pp 26938-26945 (2020)
Externí odkaz:
https://doaj.org/article/24c58b69e6564c83a9c0adb3820d2b5f
Autor:
Atsushi Ohtaka, Misa Kawase, Akira Usami, Shiho Fukui, Mana Yamashita, Kazuki Yamaguchi, Akira Sakon, Tomoya Shiraki, Taiki Ishida, Soma Nagata, Yuji Kimura, Go Hamasaka, Yasuhiro Uozumi, Tsutomu Shinagawa, Osamu Shimomura, Ryôki Nomura
Publikováno v:
ACS Omega, Vol 4, Iss 13, Pp 15764-15770 (2019)
Externí odkaz:
https://doaj.org/article/2ced352c4a5844c7ba76d499819f268d
Autor:
Atsushi Ohtaka, Misa Kawase, Shunichiro Aihara, Yasuhiro Miyamoto, Ayaka Terada, Kenta Nakamura, Go Hamasaka, Yasuhiro Uozumi, Tsutomu Shinagawa, Osamu Shimomura, Ryôki Nomura
Publikováno v:
ACS Omega, Vol 3, Iss 8, Pp 10066-10073 (2018)
Externí odkaz:
https://doaj.org/article/907547a723014cc9bf3da855f4800ec2
Autor:
Franco King-Chi Leung, Fumitaka Ishiwari, Yoshiaki Shoji, Tsuyoshi Nishikawa, Ryohei Takeda, Yuuya Nagata, Michinori Suginome, Yasuhiro Uozumi, Yoichi M. A. Yamada, Takanori Fukushima
Publikováno v:
ACS Omega, Vol 2, Iss 5, Pp 1930-1937 (2017)
Externí odkaz:
https://doaj.org/article/394a5df715034120a13afab84f6f198a
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 5, Iss 1, p 18 (2009)
A miniflow system for oxidative cyclization of alkenols with Oxone was developed. Thus, the oxidative cyclization of (Z)- and (E)-alkenols in i-PrOH with an aqueous solution of Oxone proceeded smoothly and safely in a PTFE tube without any exogenous
Externí odkaz:
https://doaj.org/article/c0fadb6ab6c845318bb10aeac76bd86d
Publikováno v:
Chemistry Letters; May2024, Vol. 53 Issue 5, p1-4, 4p
Autor:
Raghu N. Dhital, Abhijit Sen, Hao Hu, Rikako Ishii, Takuma Sato, Yoko Yashiroda, Hiromi Kimura, Charles Boone, Minoru Yoshida, Yushi Futamura, Hiroyuki Hirano, Hiroyuki Osada, Daisuke Hashizume, Yasuhiro Uozumi, Yoichi M.A. Yamada
Publikováno v:
ACS Omega. 7:24184-24189
In this study, a phenylboronic ester-activated aryl iodide-selective Buchwald-Hartwig-type amination was developed. When the reaction of aryl iodides and aryl/aliphatic amines using Ni(acac)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::109c701275e6326c6d79f84e22a3e8b2
https://doi.org/10.1021/acsomega.2c01092
https://doi.org/10.1021/acsomega.2c01092
Publikováno v:
Chemistry – A European Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bcfa15a53a8b1f9ec78a287149202fa
https://doi.org/10.1002/chem.202300840
https://doi.org/10.1002/chem.202300840
Cross-pinacol coupling of two different carbonyl compounds was achieved through successive one-electron transfer processes under photocatalytic conditions. In this process, an umpoled anionic carbinol synthon was generated in situ to react nucleophil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14008ab1f0af0e93dc5f02914992d3ca
https://doi.org/10.26434/chemrxiv-2022-jpx09
https://doi.org/10.26434/chemrxiv-2022-jpx09
Publikováno v:
Synlett. 33:40-44
A cyanide-free aromatic cyanation was developed that uses nitromethane as a cyanide source in water with an amphiphilic polystyrene–poly(ethylene glycol) resin-supported palladium catalyst and an alkyl halide (1-iodobutane). The cyanation proceeds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4acc6509656826ffac30cbff267c4d7c
https://doi.org/10.1055/a-1675-0018
https://doi.org/10.1055/a-1675-0018