2015
DOI: 10.1016/j.tetlet.2014.12.146
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FeCl 3 -catalyzed selective acylation of amines with 1,3-diketones via C–C bond cleavage

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Cited by 31 publications
(10 citation statements)
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“…The title compound was obtained as colorless crystals (21 mg, 39%) with a melting temperature of 402 K (129°C). The compound is known and its spectral data correspond to those reported in literature [2]. Single crystals were obtained by slow evaporation from ethyl acetate.…”
Section: Source Of Materialssupporting
confidence: 54%
“…The title compound was obtained as colorless crystals (21 mg, 39%) with a melting temperature of 402 K (129°C). The compound is known and its spectral data correspond to those reported in literature [2]. Single crystals were obtained by slow evaporation from ethyl acetate.…”
Section: Source Of Materialssupporting
confidence: 54%
“…[23] The concept explored further in the following years, but there are several drawbacks and limitations in the reported protocols such as narrow scope, high activity of ketone substrate, hazardous and expensive reagents, and use of radical initiators. [24][25][26][27][28][29] Moreover, in spite of the application of many homogeneous and heterogeneous catalysts designed for this process, almost all of them could not overcome the obstacle of inactivity of the simple ketones in the procedure. [24][25][26][27] Recently a novel protocol for synthesis of amides from ketones taking advantage of the C-C bond cleavage strategy has been devised which avoids This article is dedicated to memory of Naser Shabani.…”
Section: Introductionmentioning
confidence: 99%
“…To continue our research on C-N bond forming reactions [59][60][61][62][63][64][65], we sought to broaden dicarbonyl scope and study the application of the cycloaddition products found as key intermediates in the synthesis of biologically active compounds. Herein, we present a full account of our recent work on the Pd-catalyzed [4+1] annulation reaction.…”
Section: Introductionmentioning
confidence: 99%