2017
DOI: 10.1002/ejoc.201601493
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Erythrosine B Catalyzed Visible‐Light Photoredox Arylation–Cyclization of N‐Alkyl‐N‐aryl‐2‐(trifluoromethyl)acrylamides to 3‐(Trifluoromethyl)indolin‐2‐one Derivatives

Abstract: 3-Trifluoromethylindoline-2-one derivatives were prepared in a visible-light photocatalytic transformation of acrylamides. The arylation-cyclization sequence was initiated

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Cited by 37 publications
(28 citation statements)
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“…NaOTs from diphenyliodonium triflate ( 1a ) . (3‐trifluoromethylphenyl)(2,4,6‐trimethoxyphenyl)iodonium triflate ( 4c ) was synthesized by adapting the literature procedure of Stuart et al Most of the N ‐acrylamides 2 were prepared from the corresponding anilines by adapting a method published by Gulder et al N ‐Methyl‐ N ‐phenyl‐2‐(trifluoromethyl)acrylamide was prepared according to a report from Novák and Tóth . Proton nuclear magnetic resonance spectra ( 1 H NMR), carbon spectra ( 13 C NMR) and fluorine spectra ( 19 F NMR) were recorded at 400 and 250 MHz ( 1 H), 126 MHz, 75 MHz ( 13 C), 471 MHz, 282 MHz ( 19 F), respectively.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…NaOTs from diphenyliodonium triflate ( 1a ) . (3‐trifluoromethylphenyl)(2,4,6‐trimethoxyphenyl)iodonium triflate ( 4c ) was synthesized by adapting the literature procedure of Stuart et al Most of the N ‐acrylamides 2 were prepared from the corresponding anilines by adapting a method published by Gulder et al N ‐Methyl‐ N ‐phenyl‐2‐(trifluoromethyl)acrylamide was prepared according to a report from Novák and Tóth . Proton nuclear magnetic resonance spectra ( 1 H NMR), carbon spectra ( 13 C NMR) and fluorine spectra ( 19 F NMR) were recorded at 400 and 250 MHz ( 1 H), 126 MHz, 75 MHz ( 13 C), 471 MHz, 282 MHz ( 19 F), respectively.…”
Section: Methodsmentioning
confidence: 99%
“…[46] (3-trifluoromethylphenyl)(2,4,6-trimethoxyphenyl)iodonium triflate (4c) was synthesized by adapting the literature procedure of Stuart et al [42] Most of the N-acrylamides 2 were prepared from the corresponding anilines by adapting a method published by Gulder et al [48] N-Methyl-N-phenyl-2-(trifluoromethyl)acrylamide was prepared according to a report from Novák and Tóth. [49] Proton nuclear magnetic resonance spectra ( 1 H NMR), carbon spectra ( 13 C NMR) and fluorine spectra ( Melting points are reported uncorrected. The solvent given in brackets after the melting point is the last solvent the compound was treated with (e.g.…”
Section: Methodsmentioning
confidence: 99%
“…In 2013, Zou and coworkers reported a visible‐light‐mediated diarylation of N‐arylacrylamides for the synthesis of oxindoles with simultaneous construction of two C−C bond (Scheme ), wherein the aryl radical was produced via Ru 2+ * reducing the aryl diazonium salts to initiate the radical cascade cyclization. An analogous visible‐light‐induced arylation/cyclization cascade was presented by Tóth with the organic erythrosine B being applied as photocatalyst …”
Section: Synthesis Of Bicyclic Ringsmentioning
confidence: 98%
“…Cyclization of N -arylacrylamides 86 have been found as a useful strategy in the synthesis of indolin-2-one compounds 88 . Novák and Tóth group developed cyclization of trifluoromethylated acrylamides under visible-light conditions catalyzed by Erythrosine B 18b (Scheme 10) [45]. The elaborated arylation/cyclization sequence is initiated by aryl radical generation from diazonium salt 87 , which undergoes addition to the double bond of 86 followed by radical cyclization.…”
Section: Application Of Visible-light-mediated Catalysis In Synthementioning
confidence: 99%