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Volumn 38, Issue 1, 2009, Pages 42-43

Simple and efficient metal-free hydroarylation and hydroalkylation using strongly acidic ion-exchange resin

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EID: 64549121304     PISSN: 03667022     EISSN: 13480715     Source Type: Journal    
DOI: 10.1246/cl.2009.42     Document Type: Article
Times cited : (30)

References (23)
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    • Part 177 in the series, Studies on novel synthetic methodologies.
    • Part 177 in the series, Studies on novel synthetic methodologies.
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    • G. Bhalla, J. Oxgaard. W. A. Goddard, R. A. Periana, Organomet al.ics 2005, 24, 3229.
    • G. Bhalla, J. Oxgaard. W. A. Goddard, R. A. Periana, Organomet al.ics 2005, 24, 3229.
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    • 67650394244 scopus 로고    scopus 로고
    • K. Merlins, I. Jovel. J. Kisehel. A. Zapf, M. Belief. Angew. Chem., Int. Ed. 2005, 44, 238.
    • K. Merlins, I. Jovel. J. Kisehel. A. Zapf, M. Belief. Angew. Chem., Int. Ed. 2005, 44, 238.
  • 17
  • 22
    • 67650354896 scopus 로고    scopus 로고
    • 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.
    • 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.
  • 23
    • 67650369876 scopus 로고    scopus 로고
    • Supporting Information is available electrically on the CSJ-Journal Web site, http://www.csj.jp/journals/chem-lett/index.html.
    • Supporting Information is available electrically on the CSJ-Journal Web site, http://www.csj.jp/journals/chem-lett/index.html.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.