2014
DOI: 10.1016/j.tetlet.2014.09.116
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Improved methods for the synthesis and isolation of imidazolium based ionic salts

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Cited by 11 publications
(12 citation statements)
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“…The ligand precursor (1a: R=Me) was first reported by Hermann et al [25] and later by others [7a,26] and recently we have reported a quick throughput solvent free method for the synthesis and isolation of imidazolium salts that include 1a and 1b [27]. Our procedure alleviated all the limitations associated with the purification and isolation of imidazolium salts using previously reported methods [26a,28].…”
Section: Synthesis and Characterization Of Nhc-co Complexesmentioning
confidence: 83%
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“…The ligand precursor (1a: R=Me) was first reported by Hermann et al [25] and later by others [7a,26] and recently we have reported a quick throughput solvent free method for the synthesis and isolation of imidazolium salts that include 1a and 1b [27]. Our procedure alleviated all the limitations associated with the purification and isolation of imidazolium salts using previously reported methods [26a,28].…”
Section: Synthesis and Characterization Of Nhc-co Complexesmentioning
confidence: 83%
“…ThermoScientific Flash2000 Elemental Analyser respectively. Pincer imidazolium salts 1a and 1b; were synthesised and isolated in excellent yield using improved solvent free technique [27].…”
Section: Methodsmentioning
confidence: 99%
“…For the preparation of the salts ( 6a – 9b ), we applied a solvent‐free technique we reported earlier, which is based on the neat alkylation of neutral imidazoles, in this instance 6 – 9 by each of the two alkyl halides . Although no products were isolated in the attempted synthesis of salts 7b , 8a , and 8b , which we believe is mainly due to steric constraints associated with, especially, the bulkier 4,5‐phenanthro derivatives ( 8a and 8b ) and added flexibility of propyl iodide ( 7b ), the yields were low to moderate, and 1 H‐NMR was used to confirm identities of the new compounds.…”
Section: Resultsmentioning
confidence: 99%
“…Combined organic layers were dried over a bed of anhydrous MgSO 4 and filtered. All volatiles were removed under reduced pressure, and the crude product was purified by column chromatography, where elution with MeOH afforded pure products .…”
Section: Methodsmentioning
confidence: 99%
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