Matches in SemOpenAlex for { <https://semopenalex.org/work/W4328121511> ?p ?o ?g. }
- W4328121511 abstract "Abstract Background Amides are the essential building blocks of natural products and bioactive molecules. One of the most common structures discovered in medicinal and bioactive compounds is amide derivatives. The synthesis of N ‐(pyridin‐2‐yl)arylamide compounds has recently been assessed using various methods. In particular, there is growing interest in employing heterogeneous catalysts to catalyze organic synthesis reactions. Metal organic frameworks based on nickel centers were synthesized using the solvothermal method. The morphology, size, and catalytic activity of Ni‐based catalysts strongly depend on the substitute solvent composition in the reaction system. The structural features of the Ni‐based materials were verified using modern analytical techniques. Results Ni‐based materials were used to catalyze the synthesis of physiologically important N ‐(pyridin‐2‐yl)arylamides through an amidation reaction between 2‐aminopyridine and benzaldehyde. Temperature, reaction time, catalyst amount, reactant ratio, and solvent type were investigated as factors that influenced the catalytic activity. The optimal reaction conditions were 10 mol% Ni‐based catalysts, tetrahydrofuran as the reaction solvent, and a reaction temperature of 90 °C for 24 h. N ‐(pyridin‐2‐yl)arylamide was obtained in approximately 85% yield. The catalyst could be recovered and reused without significant loss of catalytic activity (79%) after six runs. Conclusion This study illustrated that the Ni‐based catalyst performed well in the reaction between 2‐aminopyridine and benzaldehyde formation N ‐(pyridin‐2‐yl)arylamide compound with an 85% yield. The solid catalyst was recovered and reused up to six times without any significant change in catalytic activity. © 2023 Society of Chemical Industry (SCI)." @default.
- W4328121511 created "2023-03-22" @default.
- W4328121511 creator A5017608167 @default.
- W4328121511 creator A5030832846 @default.
- W4328121511 creator A5046509522 @default.
- W4328121511 date "2023-05-02" @default.
- W4328121511 modified "2023-10-14" @default.
- W4328121511 title "Ni‐based metal organic frameworks: an efficient catalyst for the amidation reaction to obtain <i>N</i>‐(pyridin‐2‐yl)arylamides" @default.
- W4328121511 cites W1922672348 @default.
- W4328121511 cites W1970648125 @default.
- W4328121511 cites W1995030777 @default.
- W4328121511 cites W1999918445 @default.
- W4328121511 cites W2000360941 @default.
- W4328121511 cites W2005664846 @default.
- W4328121511 cites W2009859514 @default.
- W4328121511 cites W2017980572 @default.
- W4328121511 cites W2018108736 @default.
- W4328121511 cites W2023346593 @default.
- W4328121511 cites W2026806120 @default.
- W4328121511 cites W2040475272 @default.
- W4328121511 cites W2047903024 @default.
- W4328121511 cites W2056227086 @default.
- W4328121511 cites W2059158858 @default.
- W4328121511 cites W2074880731 @default.
- W4328121511 cites W2075709474 @default.
- W4328121511 cites W2076756203 @default.
- W4328121511 cites W2093771834 @default.
- W4328121511 cites W2098521212 @default.
- W4328121511 cites W2107347744 @default.
- W4328121511 cites W2126363023 @default.
- W4328121511 cites W2128708905 @default.
- W4328121511 cites W2130020235 @default.
- W4328121511 cites W2137378003 @default.
- W4328121511 cites W2139083301 @default.
- W4328121511 cites W2153861797 @default.
- W4328121511 cites W2153878082 @default.
- W4328121511 cites W2155113974 @default.
- W4328121511 cites W2159885427 @default.
- W4328121511 cites W2164723090 @default.
- W4328121511 cites W2168788420 @default.
- W4328121511 cites W2278879292 @default.
- W4328121511 cites W2301092244 @default.
- W4328121511 cites W2313824726 @default.
- W4328121511 cites W2346288052 @default.
- W4328121511 cites W2440836370 @default.
- W4328121511 cites W2466908497 @default.
- W4328121511 cites W2500290562 @default.
- W4328121511 cites W2555696278 @default.
- W4328121511 cites W2576830170 @default.
- W4328121511 cites W2743260621 @default.
- W4328121511 cites W2782916062 @default.
- W4328121511 cites W2785523804 @default.
- W4328121511 cites W2786081174 @default.
- W4328121511 cites W2808957813 @default.
- W4328121511 cites W2896638359 @default.
- W4328121511 cites W2898184057 @default.
- W4328121511 cites W2912437813 @default.
- W4328121511 cites W2938466621 @default.
- W4328121511 cites W2969758274 @default.
- W4328121511 cites W2986450614 @default.
- W4328121511 cites W3198412811 @default.
- W4328121511 cites W3217346502 @default.
- W4328121511 cites W4200614344 @default.
- W4328121511 cites W4220749138 @default.
- W4328121511 cites W4231722046 @default.
- W4328121511 cites W4254134018 @default.
- W4328121511 cites W4280639417 @default.
- W4328121511 cites W4283762373 @default.
- W4328121511 cites W4291130378 @default.
- W4328121511 cites W4295997597 @default.
- W4328121511 cites W4307645746 @default.
- W4328121511 doi "https://doi.org/10.1002/jctb.7376" @default.
- W4328121511 hasPublicationYear "2023" @default.
- W4328121511 type Work @default.
- W4328121511 citedByCount "0" @default.
- W4328121511 crossrefType "journal-article" @default.
- W4328121511 hasAuthorship W4328121511A5017608167 @default.
- W4328121511 hasAuthorship W4328121511A5030832846 @default.
- W4328121511 hasAuthorship W4328121511A5046509522 @default.
- W4328121511 hasConcept C134121241 @default.
- W4328121511 hasConcept C150394285 @default.
- W4328121511 hasConcept C161790260 @default.
- W4328121511 hasConcept C178790620 @default.
- W4328121511 hasConcept C179366358 @default.
- W4328121511 hasConcept C185592680 @default.
- W4328121511 hasConcept C191897082 @default.
- W4328121511 hasConcept C192562407 @default.
- W4328121511 hasConcept C2776701986 @default.
- W4328121511 hasConcept C2778439535 @default.
- W4328121511 hasConcept C2779692420 @default.
- W4328121511 hasConcept C2780471494 @default.
- W4328121511 hasConcept C2991944050 @default.
- W4328121511 hasConcept C544153396 @default.
- W4328121511 hasConceptScore W4328121511C134121241 @default.
- W4328121511 hasConceptScore W4328121511C150394285 @default.
- W4328121511 hasConceptScore W4328121511C161790260 @default.
- W4328121511 hasConceptScore W4328121511C178790620 @default.
- W4328121511 hasConceptScore W4328121511C179366358 @default.
- W4328121511 hasConceptScore W4328121511C185592680 @default.
- W4328121511 hasConceptScore W4328121511C191897082 @default.