Zobrazeno 1 - 10
of 335
pro vyhledávání: '"Mahito ATOBE"'
Autor:
Koichi Mitsudo, Atsushi Osaki, Haruka Inoue, Eisuke Sato, Naoki Shida, Mahito Atobe, Seiji Suga
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 20, Iss 1, Pp 1560-1571 (2024)
An electrocatalytic hydrogenation of cyanoarenes, nitroarenes, quinolines, and pyridines using a proton-exchange membrane (PEM) reactor was developed. Cyanoarenes were then reduced to the corresponding benzylamines at room temperature in the presence
Externí odkaz:
https://doaj.org/article/4cd9417810cc431595e078ff2a690e6c
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 20, Iss 1, Pp 264-271 (2024)
Electrochemically generated amidyl radical species produced distinct inter- or intramolecular hydroamination reaction products via a proton-coupled electron transfer (PCET) mechanism. Cyclic voltammetry (CV) analysis indicated that the chemoselectivi
Externí odkaz:
https://doaj.org/article/a4e1bcf7ff0343a19a07e504f8787014
Publikováno v:
ChemElectroChem, Vol 10, Iss 23, Pp n/a-n/a (2023)
Abstract The electrochemical [3+2] cycloaddition of phenols and alkenes in a laminar‐flow microreactor was realized at an unprecedentedly low electrolyte concentration (0.001–0.01 M) owing to low solution resistance derived from the narrow electr
Externí odkaz:
https://doaj.org/article/b7f618cca27c45648fb37abcd707a364
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 18, Iss 1, Pp 350-359 (2022)
We have successfully synthesized piperidine and pyrrolidine derivatives by electroreductive cyclization using readily available imine and terminal dihaloalkanes in a flow microreactor. Reduction of the substrate imine on the cathode proceeded efficie
Externí odkaz:
https://doaj.org/article/e541747853ac4b69b041010a5f736aa0
Publikováno v:
Electrochemistry, Vol 91, Iss 11, Pp 112003-112003 (2023)
β-Scission from alkoxy radical enables selective Csp3-Csp3 bond cleavage under ambient conditions, offering a useful method for organic synthesis. Various photocatalytic systems for β-scission have been reported, where proton-coupled electron trans
Externí odkaz:
https://doaj.org/article/50288f0d6ee9483faa17142c4a675b97
Publikováno v:
Electrochemistry, Vol 91, Iss 11, Pp 112006-112006 (2023)
Herein, we report that the 2,7-dimethoxynaphthyl (2,7-DMN) group is a novel electroauxiliary that is readily installed at the N-α position of a carbamate through Friedel–Crafts-type arylation. The resulting N-α C–C bond is easily cleaved throug
Externí odkaz:
https://doaj.org/article/9ca51f6784ea4717b64da60d56640e30
Publikováno v:
Electrochemistry, Vol 91, Iss 11, Pp 112002-112002 (2023)
Redox behavior is a fundamental and fascinating feature of polycyclic aromatic hydrocarbons (PAHs). Cyclic voltammetry (CV) measurements are commonly performed to estimate the electronic structure of PAHs and to determine the stability of their oxida
Externí odkaz:
https://doaj.org/article/c8a339b8578a4181b2254cd1845c5075
Publikováno v:
Electrochemistry, Vol 91, Iss 11, Pp 112016-112016 (2023)
Photocatalytic single-electron transfer (SET) reactions involving perfluoroalkyl halides play a crucial role in synthetic organic chemistry. However, the electrochemical data for these compounds, which are essential in the discussion of the SET proce
Externí odkaz:
https://doaj.org/article/a2512d6827fc416d9a3dba756a74b730
Autor:
Mahito ATOBE, Minoru MIZUHATA
Publikováno v:
Electrochemistry, Vol 89, Iss 6, Pp 485-490 (2021)
The Electrochemical Society of Japan (ECSJ) has been publishing comprehensive papers related to the achievements of researchers who are awarded by ECSJ annually since 2014. The origin of the society awards, we can see that they began as Tanahashi Pap
Externí odkaz:
https://doaj.org/article/718ee0a96ab7462ebc3011077f56829f
Publikováno v:
Electrochemistry, Vol 89, Iss 4, Pp 395-399 (2021)
In this study, we report one step electrochemical trimerization of catechol to 2,3,6,7,10,11-hexahydroxytriphenylene (HHTP) for the first time. Electrochemical trimerization was demonstrated in a flow microreactor, which offers advantages for reactio
Externí odkaz:
https://doaj.org/article/ee523886a3bf4f97b9ecf9e19cf27fc0