Zobrazeno 1 - 10
of 172
pro vyhledávání: '"Yoshihiro Nishimoto"'
Autor:
Tomomasa FUNAKOSHI, Sou WATANABE, Yoichi ARAI, Toshihiro IWAMOTO, Masayuki WATANABE, Yoshihiro NISHIMOTO, Makoto YASUDA
Publikováno v:
Mechanical Engineering Journal, Vol 11, Iss 2, Pp 23-00445-23-00445 (2024)
Various types of machine oil are used for analysis and utility equipment, and these organic liquid wastes are stored in nuclear facilities and laboratories due to a lack of appropriate treatment processes. Treatment of organic liquid waste is one of
Externí odkaz:
https://doaj.org/article/1a500ec7f83346eeae2080266f10d3a3
Autor:
Satoru Yoshimura, Yoshihiro Nishimoto, Masato Kiuchi, Yoshiaki Agawa, Hiroyuki Tanaka, Makoto Yasuda
Publikováno v:
AIP Advances, Vol 7, Iss 6, Pp 065117-065117-9 (2017)
Indium nano-particle irradiations onto zeolite powders were carried out using a pulse arc plasma source system. X-ray photoelectron spectroscopic and scanning electron microscopic studies of an indium irradiated zeolite sample revealed that indium na
Externí odkaz:
https://doaj.org/article/0295819e0cc84e388867aa8fbd75f8c4
Publikováno v:
Molecules, Vol 23, Iss 8, p 1884 (2018)
Regioselective anti-allylindation of alkynes was achieved using InBr3 and allylic silanes. Various types of alkynes and allylic silanes were applicable to the present allylindation. This sequential process used the generated 1,4-dienylindiums to esta
Externí odkaz:
https://doaj.org/article/212df39a030146e19b45de3b791b5cc5
Publikováno v:
Molecules, Vol 21, Iss 10, p 1330 (2016)
The substitution of a siloxy group using thiosilanes smoothly occurred in the presence of InI3 catalyst to yield the corresponding thioethers. InI3 was a specifically effective catalyst in this reaction system, while other typical Lewis acids such as
Externí odkaz:
https://doaj.org/article/8c935c5d668b4ba5a4db0fedbd7dc63a
Publikováno v:
Chemistry Letters. 52:79-83
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db6fefcc1923eaf1aa84f5ecbdbf4e3f
https://doi.org/10.1246/cl.220488
https://doi.org/10.1246/cl.220488
Publikováno v:
Organic Letters. 25:766-770
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd84349a8984c0d33026b71b883ea903
https://doi.org/10.1021/acs.orglett.2c04235
https://doi.org/10.1021/acs.orglett.2c04235
Publikováno v:
Organic Letters. 24:1706-1710
One-carbon-unit insertion into carbon-halogen (C-X) bonds accompanied by the formation of a new C-X bond and carbon-chain elongation is a powerful synthetic method of complex organohalides. Herein, we developed an indium trihalide catalyzed formal in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af12b2ffd84c2b18dab3c5b6abced436
https://doi.org/10.1021/acs.orglett.2c00343
https://doi.org/10.1021/acs.orglett.2c00343
Publikováno v:
Synthesis. 54:2765-2777
Due to its large bond energy, precisely controllable C–F bond activation is a significant challenge in organic synthesis. A single C(sp3)–F bond transformation of perfluoroalkyl groups is particularly desirable to supply functionalized perfluoroa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::493e2cff94c395394d43ac613520a2dd
https://doi.org/10.1055/a-1755-3476
https://doi.org/10.1055/a-1755-3476
Publikováno v:
Journal of the American Chemical Society. 143:20616-20621
Selective transformation of C-F bonds remains a significant goal in organic chemistry, but C-F insertion of a one-carbon-atom unit has never been established. Herein we report the BF3-catalyzed formal insertion of diazo esters as one-carbon-atom sour
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::008858f210b4c3593e332d44bcabb586
https://doi.org/10.1021/jacs.1c10517
https://doi.org/10.1021/jacs.1c10517
Autor:
Yoshihiro Nishimoto1 nishimoto@chem.eng.osaka-u.ac.jp, Makoto Yasuda1 yasuda@chem.eng.osaka-u.ac.jp
Publikováno v:
Chemistry - An Asian Journal. 3/16/2020, Vol. 15 Issue 6, p636-650. 15p.