2006
DOI: 10.1002/chin.200646132
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Novel Carbon—Carbon Bond Formation Between N‐Methyl‐3‐phenyl‐3‐hydroxypropylamine and Cresols Catalyzed by p‐Toluenesulfonic Acid.

Abstract: Acid. -The TosOH-catalyzed condensation of amino alcohol (I) with cresols affords the C-arylated products (III) instead of the expected phenol ethers (yields not given). -(GOPALAKRISHNAN*, M.; SURESHKUMAR, P.; KANAGARAJAN, V.; THANUSU, J.; GOVINDAN, S.; GHANTA, M. R.; Synth.

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Cited by 4 publications
(6 citation statements)
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“…Many solvent-assisted brominating methods for the bromination of alkyl and aryl compounds by direct use of bromine solution in alkaline or acid medium have been reported in the literature [3,[41][42][43]. In the present work, the author has attempted to brominate naphthyl keto compounds with an alternative reagent like Winkler's solution (bromate-bromide solution) in the presence of aqueous phase catalyst fly-ash.…”
Section: Resultsmentioning
confidence: 99%
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“…Many solvent-assisted brominating methods for the bromination of alkyl and aryl compounds by direct use of bromine solution in alkaline or acid medium have been reported in the literature [3,[41][42][43]. In the present work, the author has attempted to brominate naphthyl keto compounds with an alternative reagent like Winkler's solution (bromate-bromide solution) in the presence of aqueous phase catalyst fly-ash.…”
Section: Resultsmentioning
confidence: 99%
“…In the present work, the author has attempted to brominate naphthyl keto compounds with an alternative reagent like Winkler's solution (bromate-bromide solution) in the presence of aqueous phase catalyst fly-ash. The bromate-bromide solution was harmless to the reaction [3,[41][42][43] as well as the environment. Various 1-naphthyl ketones containing electron withdrawing and electron donating groups in position 4 have been subjected to bromination at acyl methyl group with Winkler's solution in the presence of fly-ash catalyst under water medium (Scheme 1).…”
Section: Resultsmentioning
confidence: 99%
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“…Many researchers studied the potential activity of fly ash and the hydration process of fly-ash cement [3]. Recently microwave-assisted activated fly-ash catalyzed Knoevenagel condensation, synthesis of amides, Schiff bases formation, Biginelli and Hantzsch reactions have been reported [4]. In addition, activated fly ash is used for the "one-pot" synthesis of 1,2,4,5-tetrazines [5] and 1,2,3-selenadiazoles [6].…”
Section: Introductionmentioning
confidence: 99%
“…Owing to the necessity of the "environmentally safe technological revolution" [8] a considerable attention is given to the procedure of microwave irradiation for ensuring fast synthesis of versatile organic compounds because of selective absorption of the microwave energy by polar molecules. The use of heterogeneous catalysts, in particular, NaHSO 4 on SiO 2 carrier [9], became a milestone in various fields of chemistry due to environmental safety combined with good yields and selectivity.…”
mentioning
confidence: 99%