“…The arylhydrazone was obtained as a pale yellow solid (93%). 1 H and 13 C NMR are in accordance with the literature data. [24] N-p-Trifluoromethylphenyl Benzophenone Hydrazone…”
Section: General Procedures For the Palladium-catalyzed Coupling Reactsupporting
confidence: 91%
“…1 H and 13 C NMR spectra were determined on a 200 MHz spectrometer. Melting points were determined on a Büchi B-545 capillary melting point apparatus and are uncorrected.. Each compound prepared herein was characterized by GC, GC-MS and 1 H NMR spectroscopy.…”
Section: Experimental Section General Proceduresmentioning
confidence: 99%
“…[1] Thus, they are important to a diverse array of fields, such as agrochemicals, pharmaceuticals or photography.…”
Various arylhydrazones have been successfully synthesized via a highly efficient palladium-catalyzed cross-coupling reaction between aryl halides and benzophenone hydrazone. All the reaction parameters have been studied and coupling products were obtained with excellent yields from the corresponding bromides or chlorides.
“…The arylhydrazone was obtained as a pale yellow solid (93%). 1 H and 13 C NMR are in accordance with the literature data. [24] N-p-Trifluoromethylphenyl Benzophenone Hydrazone…”
Section: General Procedures For the Palladium-catalyzed Coupling Reactsupporting
confidence: 91%
“…1 H and 13 C NMR spectra were determined on a 200 MHz spectrometer. Melting points were determined on a Büchi B-545 capillary melting point apparatus and are uncorrected.. Each compound prepared herein was characterized by GC, GC-MS and 1 H NMR spectroscopy.…”
Section: Experimental Section General Proceduresmentioning
confidence: 99%
“…[1] Thus, they are important to a diverse array of fields, such as agrochemicals, pharmaceuticals or photography.…”
Various arylhydrazones have been successfully synthesized via a highly efficient palladium-catalyzed cross-coupling reaction between aryl halides and benzophenone hydrazone. All the reaction parameters have been studied and coupling products were obtained with excellent yields from the corresponding bromides or chlorides.
“…Various substituted enynes were shown to undergo intramolecular cycloaddition reactions providing a new pathway to bicyclic products. [1][2][3][4] The proposed mechanism of the reaction is interesting. The six-membered allene (1,2,4-cyclohexatriene and its derivatives) were suggested as reaction intermediates (Scheme 1).…”
“…The prominent examples are ketorolac, tolmetin and indomethacin [1]. In view of the importance of these compounds substantial attention has been paid to their synthesis, which proceeds mainly via cycloaddition or cycloisomerization of acyclic precursors [2][3][4][5]. Besides, the conjugate addition of nucleophiles to α,β-unsaturated compounds is one of the most powerful bond forming strategies and has been widely utilized in the field of heterocyclic chemistry.…”
A new class of 3,4-disubstituted pyrroles has been prepared by the reaction of 1-aroyl-2-arylsulfonylethenes and 1,2-diarylsulfonylethenes with tosyl methyl isocyanide.
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