Zobrazeno 1 - 10
of 312
pro vyhledávání: '"Yasushi, Nishihara"'
Publikováno v:
The Journal of Organic Chemistry. 88:4472-4480
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cda294edc152f0f8f4151c563ae1cacf
https://doi.org/10.1021/acs.joc.2c03081
https://doi.org/10.1021/acs.joc.2c03081
Publikováno v:
ACS Omega, Vol 3, Iss 10, Pp 13129-13140 (2018)
Externí odkaz:
https://doaj.org/article/5eb6110e94554d2ebaf17eae4aebf86f
Autor:
Qiang Chen, Jingwen You, Tian Tian, Zhenyao Li, Myuto Kashihara, Hiroki Mori, Yasushi Nishihara
Publikováno v:
Organic Letters. 24:9259-9263
This paper describes the nickel-catalyzed reductive alkylation of aroyl fluorides with alkyl bromides in a decarbonylative manner. In this reaction, various functional groups are well tolerated and the C(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfc2d42915f157811fd06692dad989e0
https://doi.org/10.1021/acs.orglett.2c03823
https://doi.org/10.1021/acs.orglett.2c03823
Publikováno v:
ACS Omega, Vol 2, Iss 1, Pp 308-315 (2017)
Externí odkaz:
https://doaj.org/article/d3074075929341d8a08e1103b4b7188d
Publikováno v:
Polymer Journal. 55:405-415
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e18d20cd4e7e4cec05a314d191f96c9
https://doi.org/10.1038/s41428-022-00706-z
https://doi.org/10.1038/s41428-022-00706-z
Publikováno v:
Bulletin of the Chemical Society of Japan. 95:942-952
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba1260de1f62d86efcd5007528d0d1d9
https://doi.org/10.1246/bcsj.20220093
https://doi.org/10.1246/bcsj.20220093
Publikováno v:
Synthesis. 54:3667-3697
Numerous studies on the activation of carbon–fluorine bonds have been reported in recent years. For example, acyl fluorides have been utilized as versatile reagents for acylation, arylation, and even fluorination. In this review, we focus on acyl f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::456328a2644b2bc8b9fd3f103b4da7cd
https://doi.org/10.1055/a-1845-3810
https://doi.org/10.1055/a-1845-3810
Publikováno v:
Molecules, Vol 25, Iss 17, p 3842 (2020)
We report the design, synthesis, and physicochemical properties of an array of phenanthro[2,1-b:7,8-b’]dithiophene (PDT-2) derivatives by introducing five types of alkyl (CnH2n+1; n = 8, 10, 12, 13, and 14) or two types of decylthienyl groups at 2,
Externí odkaz:
https://doaj.org/article/ed3922163ff241f58bc67969f61f7fe3
Autor:
Atsushi Wakamiya, Takeshi Hasegawa, Natsumi Yamashita, Richard Murdey, Takafumi Shimoaka, Yasushi Nishihara, Fumiyuki Ozawa, Nobutaka Shioya, Hiroki Mori, Masayuki Wakioka
Publikováno v:
Chemistry of Materials. 33:5631-5638
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77747e5fd4139f62fd31c6a53f8826a3
https://doi.org/10.1021/acs.chemmater.1c01016
https://doi.org/10.1021/acs.chemmater.1c01016
Publikováno v:
Synthesis. 53(17):3045-3050
Nickel-catalyzed decarbonylative thioetherification of acyl fluorides has been developed. This transformation allows an array of acyl fluorides to react with thiophenols. A wide range of functional groups are well tolerated and the corresponding sulf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c0552d017aedc708fce655330242967
https://ousar.lib.okayama-u.ac.jp/62010
https://ousar.lib.okayama-u.ac.jp/62010