Zobrazeno 1 - 10
of 90
pro vyhledávání: '"Ken-ichiro Kanno"'
Publikováno v:
Inorganics, Vol 6, Iss 3, p 99 (2018)
A series of unsymmetrically substituted oligosilanes were synthesized via stepwise introduction of different substituents to α-chloro-ω-hydrooligosilanes. The reactions of α-chloro-ω-hydrooligosilanes with organolithium or Grignard reagents gave
Externí odkaz:
https://doaj.org/article/1cb1439d600e49f7920f5f22193f95e3
Autor:
Ken-ichiro Kanno, Soichiro Kyushin
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 80:574-582
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d27a8f4c3f45ff54e5bb3dc514119a4
https://doi.org/10.5059/yukigoseikyokaishi.80.574
https://doi.org/10.5059/yukigoseikyokaishi.80.574
Autor:
Ryohei Ono, Keita Osawa, Yutaka Takahashi, Yoshifumi Noguchi, Nobuo Kitada, Ryohei Saito-Moriya, Takashi Hirano, Shojiro A. Maki, Keisei Shibata, Hidefumi Akiyama, Ken-ichiro Kanno, Hideyuki Itabashi, Miyabi Hiyama
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 434:114270
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6350eac0fae50a1c8323a494eae505c
https://doi.org/10.1016/j.jphotochem.2022.114270
https://doi.org/10.1016/j.jphotochem.2022.114270
Autor:
Ryo Kumagai, Ryohei Ono, Shu Sakimoto, Chiharu Suzuki, Ken-ichiro Kanno, Hiroshi Aoyama, Junko Usukura, Masataka Kobayashi, Hidefumi Akiyama, Hideyuki Itabashi, Miyabi Hiyama
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 434:114230
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aea7928d802864c9348e9e9a019f6594
https://doi.org/10.1016/j.jphotochem.2022.114230
https://doi.org/10.1016/j.jphotochem.2022.114230
Autor:
Ken-ichiro Kanno, Seiya Noguchi, Yukie Ono, Saki Egawa, Naoki Otsuka, Masato Mita, Soichiro Kyushin
Publikováno v:
Journal of Organometallic Chemistry. 961:122234
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e1c05a6c20c9baa054d7031d488853f
https://doi.org/10.1016/j.jorganchem.2021.122234
https://doi.org/10.1016/j.jorganchem.2021.122234
Publikováno v:
ChemistrySelect. 3:4298-4302
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebae5cbeae571c7b6e46f8d1c01f2c17
https://doi.org/10.1002/slct.201800376
https://doi.org/10.1002/slct.201800376
Publikováno v:
Tetrahedron Letters. 58:9-12
Transition metal-catalyzed synthesis of alkoxydisilanes via dehydrogenative coupling of a hydrodisilane with alcohols is reported. During the reaction, the Si Si bond is preserved effectively when [RuCl2(p-cymene)]2 is used as a catalyst. Various alc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a61e96022a4ea71634b6d490547f07e
https://doi.org/10.1016/j.tetlet.2016.11.073
https://doi.org/10.1016/j.tetlet.2016.11.073
Publikováno v:
Tetrahedron Letters. 61:152274
Ruthenium-catalyzed hydrosilylation of alkynes was applied to hydrooligosilanes to furnish alkenyloligosilanes without Si–Si bond cleavage in good yields. The (E)- and α-adducts were obtained regio- and stereoselectively by using RuHCl(CO)(PPh3)3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b904f142277c7c74c1c565a6b5b1af1b
https://doi.org/10.1016/j.tetlet.2020.152274
https://doi.org/10.1016/j.tetlet.2020.152274
Autor:
Kiyohiko Nakajima, Ken-ichiro Kanno, Tamotsu Takahashi, Eri Igarashi, Yuki Mizukami, Zhiyi Song
Publikováno v:
Organic Letters. 18:6217-6219
The highly selective synthesis of triene derivatives was achieved by a zirconocene-mediated three-component coupling reaction, and the trienes were efficiently subjected to 7-endo mode cyclization. The reaction of unsymmetrical zirconacyclopentadiene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad3e8ceee89a36e917062f3d4b126fde
https://doi.org/10.1021/acs.orglett.6b02956
https://doi.org/10.1021/acs.orglett.6b02956
Publikováno v:
Tetrahedron Letters. 54:6940-6943
Transition metal-catalyzed monoreduction of dichlorooligosilanes with Grignard reagents is reported. Among the examined catalysts, group 4 metal chlorides such as TiCl 4 and Cp 2 TiCl 2 gave the highest reactivity and good selectivity. The reducing p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebce8bbe8e5ccd360fc4cdf433a4f38f
https://doi.org/10.1016/j.tetlet.2013.10.050
https://doi.org/10.1016/j.tetlet.2013.10.050