메뉴 건너뛰기




Volumn 4, Issue 18, 2002, Pages 3031-3033

New Palladium Carbene Catalysts for the Heck Reaction of Aryl Chlorides in Ionic Liquids

Author keywords

[No Author keywords available]

Indexed keywords

CHLORINATED HYDROCARBON; CINNAMIC ACID DERIVATIVE; ION; PALLADIUM; QUATERNARY AMMONIUM DERIVATIVE; SOLVENT; STILBENE DERIVATIVE; TETRABUTYLAMMONIUM;

EID: 0037026459     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol020103h     Document Type: Article
Times cited : (295)

References (59)
  • 5
    • 33750236967 scopus 로고
    • (a) Herrmann, W. A.; Brossmer, C.; Öfele, K.; Priermeier, T.; Beller, M.; Fischer, H. Angew. Chem. 1995, 107, 1989; Angew. Chem., Int. Ed. Engl. 1995, 34, 1844.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 1844
  • 7
    • 33748233333 scopus 로고
    • (b) Beller, M.; Fischer, H.; Herrmann, W. A.; Brossmer, C. Angew. Chem. 1995, 107, 1992; Angew. Chem., Int. Ed. Engl. 1995, 34, 1848.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 1848
  • 23
    • 0037090921 scopus 로고    scopus 로고
    • (j) Gstöttmayr, C. W. K.; Böhm, V. P. W.; Herdtweck, E.; Grosche, M.; Herrmann, W. A. Angew. Chem. 2002, 114, 1421; Angew. Chem., Int. Ed. 2002, 41, 1363.
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 1363
  • 28
    • 0034680642 scopus 로고    scopus 로고
    • (b) Zapf, A.; Ehrentraut, A.; Beller, M. Angew. Chem. 2000, 112, 4315; Angew. Chem., Int. Ed. 2000, 39, 4153.
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 4153
  • 33
    • 0035800382 scopus 로고    scopus 로고
    • (a) Mägerlein, W.; Indolese, A.; Beller, M. Angew. Chem. 2001, 113, 2940; Angew. Chem., Int. Ed. 2001, 40, 2856.
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 2856
  • 47
    • 0037087570 scopus 로고    scopus 로고
    • (a) Jackstell, R.; Gómez Andreu, M.; Frisch, A.; Selvakumar, K.; Zapf, A.; Klein, H.; Spannenberg, A.; Röttger. D.; Briel, O.; Karch, R.; Beller, M. Angew. Chem. 2002, 114, 1028; Angew. Chem., Int. Ed. 2002, 41, 986.
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 986
  • 54
    • 33748647785 scopus 로고
    • (a) de Meijere, A.; Meyer, F. E. Angew. Chem. 1994, 106. 2473; Angew. Chem., Int. Ed. Engl. 1994, 33, 2379.
    • (1994) Angew. Chem., Int. Ed. Engl. , vol.33 , pp. 2379
  • 56
    • 0442263465 scopus 로고    scopus 로고
    • note
    • Standard reaction conditions: 1 mmol of aryl chloride, 1.5 mmol of olefin, 1.2 mmol of sodium acetate, catalyst (0.5 mol %), and 2 g of tetrabutylammonium bromide were stirred under argon at 140°C for 24 h in a Schlenk tube. After the mixture was cooled, the internal standard (diethyleneglycol di-n-butyl ether) was added, and the mixture was diluted with 5 mL of water and extracted with 3 × 5 mL of ether. The combined organic layers were dried over sodium sulfate. The conversion and the yield were determined by gas chromatography.
  • 59
    • 0000034575 scopus 로고    scopus 로고
    • (b) Wasserscheid, P.; Keim, W. Angew. Chem. 2000, 112, 3926; Angew. Chem., Int. Ed. 2000, 39, 3772.
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 3772


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.