Zobrazeno 1 - 10
of 544
pro vyhledávání: '"Feng‐Ling Qing"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 19, Iss 1, Pp 1372-1378 (2023)
A visible-light-induced nickel-catalyzed cross coupling of alkyl carboxylic acids with N-trifluoroethoxyphthalimide is described. Under purple light irradiation, an α-hydroxytrifluoroethyl radical generated from a photoactive electron donor–accept
Externí odkaz:
https://doaj.org/article/2e77eafc2b404d8caeb19cf1966e7f8f
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 657-662 (2020)
A cascade oxidative trifluoromethylthiolation and cyclization of N-[(3-aryl)propioloyl]indoles with AgSCF3 is described. This protocol allows for the synthesis of novel bis(trifluoromethylthiolated) or trifluoromethylthiolated pyrrolo[1,2-a]indol-3-o
Externí odkaz:
https://doaj.org/article/185b8f84f5c742489e8aa77248da6a70
Publikováno v:
The Journal of Organic Chemistry. 88:4434-4441
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-7 (2018)
To date the carboacylation of alkenes has been reported only in single- and two-component methodologies. Here, the authors report a three-component nickel-catalyzed carboacylation of olefins which enables the rapid construction of ketones with high l
Externí odkaz:
https://doaj.org/article/e47c110e45244dd8aba2aefe8589ec40
Publikováno v:
SCIENTIA SINICA Chimica. 53:537-543
Publikováno v:
Organic Letters. 24:9332-9336
A photochemically induced nickel-catalyzed radical cross-coupling of phthalimido trifluoroethanol with aryl bromides to furnish α-aryl-α-trifluoromethyl alcohols is reported. This reaction proceeds via a photoinduced charge transfer of an electron
Publikováno v:
Chinese Journal of Chemistry. 40:2956-2962
Publikováno v:
CCS Chemistry. 4:2518-2549
Publikováno v:
Chinese Journal of Chemistry; Nov2023, Vol. 41 Issue 21, p2779-2787, 9p
Publikováno v:
Chinese Chemical Letters. 33:817-820
An iron-catalyzed coupling reaction of difluoroenol silyl ethers and cyclobutanone oxime esters is described. This protocol provides a convenient access to various previously unknown and potentially useful gem-difluoromethylenated ketonitriles inmode