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67650361105
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Part 177 in the series, Studies on novel synthetic methodologies.
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Part 177 in the series, Studies on novel synthetic methodologies.
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0347594386
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67650354896
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General procedure for hydroarytation and hydroalkylation: To a stirred solution of an arene or 1.3-dicarbonyl compound (1 mmol) and styrene (1.1mmol) Amberlyst-15 (100mg) was added. The mixture was allowed to reflux at 80 °C and the reaction was monitored by TLC. After completion the mixture was cooled and filtered. The filtrate was concentrated and the residue was subjected to column chromatography (silica get, hexane-EtOAc) to obtain pure hydroarylated or hydroalkylated styrene. The catalytic efficiency of Amberlyst-15 was tested on the reaction of styrene and 2-naphlhol (Table 1, Entry a) following the above method. The yields of 3a were found to be 98, 96, 95, and 92% in four consecutive uses of the catalyst.
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General procedure for hydroarytation and hydroalkylation: To a stirred solution of an arene or 1.3-dicarbonyl compound (1 mmol) and styrene (1.1mmol) Amberlyst-15 (100mg) was added. The mixture was allowed to reflux at 80 °C and the reaction was monitored by TLC. After completion the mixture was cooled and filtered. The filtrate was concentrated and the residue was subjected to column chromatography (silica get, hexane-EtOAc) to obtain pure hydroarylated or hydroalkylated styrene. The catalytic efficiency of Amberlyst-15 was tested on the reaction of styrene and 2-naphlhol (Table 1, Entry a) following the above method. The yields of 3a were found to be 98, 96, 95, and 92% in four consecutive uses of the catalyst.
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67650369876
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Supporting Information is available electrically on the CSJ-Journal Web site, http://www.csj.jp/journals/chem-lett/index.html.
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Supporting Information is available electrically on the CSJ-Journal Web site, http://www.csj.jp/journals/chem-lett/index.html.
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