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Volumn 100, Issue 8, 2000, Pages 3009-3066

Heck reaction as a sharpening stone of palladium catalysis

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL BONDS; COMPLEXATION; MICROWAVE HEATING; OLEFINS; OXIDATION; PALLADIUM; PHASE EQUILIBRIA; PHOSPHORUS COMPOUNDS; PRESSURE EFFECTS; SALTS; SUPERCRITICAL FLUIDS;

EID: 0034249671     PISSN: 00092665     EISSN: None     Source Type: Journal    
DOI: 10.1021/cr9903048     Document Type: Article
Times cited : (3949)

References (419)
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    • Heck, R. F. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 4.
    • (1991) Comprehensive Organic Synthesis , vol.4
    • Heck, R.F.1
  • 7
    • 0003837555 scopus 로고    scopus 로고
    • Liebeskind, L. S., Ed.; Jai Press Inc: Greenwich, CT
    • Jeffery, T. In Advances in Metal-Organic Chemistry; Liebeskind, L. S., Ed.; Jai Press Inc: Greenwich, CT, 1996; Vol. 5.
    • (1996) Advances in Metal-Organic Chemistry , vol.5
    • Jeffery, T.1
  • 15
    • 0003748618 scopus 로고    scopus 로고
    • Davies, S. G., Murahashi, S.-I., Eds.; Blackwell Sci.: Oxford
    • Reetz, M. T. In Transition Metal Catalyzed Reactions; Davies, S. G., Murahashi, S.-I., Eds.; Blackwell Sci.: Oxford, 1999.
    • (1999) Transition Metal Catalyzed Reactions
    • Reetz, M.T.1
  • 40
    • 0342473735 scopus 로고
    • Knipe, A. C., Watts, W. E., Eds.; John Wiley & Sons Ltd.: New York
    • Crampton, M. R. In Organic Reaction Mechanisms 1995; Knipe, A. C., Watts, W. E., Eds.; John Wiley & Sons Ltd.: New York, 1997.
    • (1995) Organic Reaction Mechanisms
    • Crampton, M.R.1
  • 83
  • 107
    • 0342908058 scopus 로고    scopus 로고
    • Z-Olefins resulting from the less favorable conformer are not sole kinetic control products. The formation of such products along with regular E-olefins in some reactions is likely to be accounted for by the rate of reductive elimination being fast on the time scale of internal rotation around the C-C bond (the anti-Curtin-Hammett kinetics)
    • Z-Olefins resulting from the less favorable conformer are not sole kinetic control products. The formation of such products along with regular E-olefins in some reactions is likely to be accounted for by the rate of reductive elimination being fast on the time scale of internal rotation around the C-C bond (the anti-Curtin-Hammett kinetics).
  • 130
    • 0342473733 scopus 로고    scopus 로고
    • As soon as postrun catalyst recovery experiments are likely to be done for reactions with reasonable loads of catalyst, and the activity of catalytic species generated is very high, it also may be argued that only a tiny fraction of palladacycle precursor underwent the cleavage into catalytically active species while the major part of it has not participated in the reaction
    • As soon as postrun catalyst recovery experiments are likely to be done for reactions with reasonable loads of catalyst, and the activity of catalytic species generated is very high, it also may be argued that only a tiny fraction of palladacycle precursor underwent the cleavage into catalytically active species while the major part of it has not participated in the reaction.
  • 268
    • 0343778821 scopus 로고    scopus 로고
    • 2 is an excellent catalyst for reactions even with nonactivated aryl bromides in a phosphine-free mode
    • 2 is an excellent catalyst for reactions even with nonactivated aryl bromides in a phosphine-free mode.
  • 323
    • 0003625966 scopus 로고
    • Wilkinson, G., Stone, F. G. A., Abel, E., Eds.; Pergamon: Oxford
    • McKillop, A. In Comprehensive Organometallic Chemistry; Wilkinson, G., Stone, F. G. A., Abel, E., Eds.; Pergamon: Oxford, 1982; Vol. 7.
    • (1982) Comprehensive Organometallic Chemistry , vol.7
    • McKillop, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.