Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Naoyuki Toriumi"'
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-8 (2022)
Hydrocarboxylation of olefins with CO2 provides a useful approach for the synthesis of aliphatic carboxylic acids. Here, the authors report a rhodium-catalysed hydrocarboxylation of styrenes with CO2, using hydrogen as the terminal reductant.
Externí odkaz:
https://doaj.org/article/44a35dba9633462294fcd523c895939c
Publikováno v:
Chemical and Pharmaceutical Bulletin. 71:462-465
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fba875e42d534f150db98397332869c1
https://doi.org/10.1248/cpb.c23-00179
https://doi.org/10.1248/cpb.c23-00179
Publikováno v:
Chemical and Pharmaceutical Bulletin. 71:459-461
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1495d7569f344445186bb9cc183b0dd5
https://doi.org/10.1248/cpb.c23-00001
https://doi.org/10.1248/cpb.c23-00001
Publikováno v:
Journal of the American Chemical Society. 144:19592-19602
Despite the recent tremendous progress on transition-metal/photoredox dual catalysis in organic synthesis, single transition-metal catalysis under visible-light irradiation, which can utilize light energy more efficiently, is still underdeveloped. He
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3c2a1e121dd082210550b822b58f6e8
https://doi.org/10.1021/jacs.2c09318
https://doi.org/10.1021/jacs.2c09318
Publikováno v:
ChemCatChem. 15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e319801f29aebbcbbe1683417526e4fc
https://doi.org/10.1002/cctc.202300139
https://doi.org/10.1002/cctc.202300139
Autor:
Shunsuke Yanagi, Akihisa Matsumoto, Naoyuki Toriumi, Yusuke Tanaka, Kazunori Miyamoto, Atsuya Muranaka, Masanobu Uchiyama
Publikováno v:
Angewandte Chemie. 135
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1022c389b0472a8eaaa0216fd4cfec5
https://doi.org/10.1002/ange.202218358
https://doi.org/10.1002/ange.202218358
Publikováno v:
European Journal of Organic Chemistry. 5/7/2021, Vol. 2021 Issue 17, p2474-2478. 5p.
Publikováno v:
Organic Letters. 23:9262-9266
A highly (Z)-selective hydroboration of terminal alkynes was achieved using a thioxanthene-based PSP-pincer rhodium catalyst. This hydroboration exhibited good chemoselectivity toward alkynes over carbonyl compounds such as ketones and aldehydes. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29535b37a1779a6331283e557bb240d2
https://doi.org/10.1021/acs.orglett.1c03606
https://doi.org/10.1021/acs.orglett.1c03606
Publikováno v:
Angewandte Chemie. 133:23537-23544
A meta-selective C-H carboxylation reaction of 1,1-diarylethylene derivatives with CO2 by using a rhodium catalyst with NaOi Pr as a stoichiometric reductant has been achieved. Together with hydrogenation of the ethylene moiety, a carboxyl group was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c77ced11d1d5873873a19e9c31c5e89
https://doi.org/10.1002/ange.202109470
https://doi.org/10.1002/ange.202109470
Publikováno v:
Chemistry – A European Journal. 27:12635-12641
A metal-free photoredox-catalyzed hydrodefluorination of fluoroarenes was achieved by using N,N,N',N'-tetramethyl-para-phenylenediamine (1) as a strong photoreduction catalyst. This reaction was applicable not only to electron-rich monofluoroarenes b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a5e3dd490d86b0ec413cd31afccb89a
https://doi.org/10.1002/chem.202101813
https://doi.org/10.1002/chem.202101813