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Volumn 27, Issue 18, 2008, Pages 4758-4771

Rhodium-catalyzed C-C coupling reactions: Mechanistic considerations

Author keywords

[No Author keywords available]

Indexed keywords

ACIDS; HYDROCARBONS; MECHANISMS; OLEFINS; PHOSPHORUS COMPOUNDS; RATE CONSTANTS; RHODIUM;

EID: 53849147213     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om800472v     Document Type: Conference Paper
Times cited : (37)

References (75)
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    • Wiedemann, S. H., Bergman, R. G., Ellman, J. A., Dyker, G., Eds.; Wiley-VCH: Weinheim, Germany, 2005; 1, pp 187-194.
    • Wiedemann, S. H., Bergman, R. G., Ellman, J. A., Dyker, G., Eds.; Wiley-VCH: Weinheim, Germany, 2005; Vol. 1, pp 187-194.
  • 59
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    • Frisch, M. J, Trucks, G. W, Schlegel, H. B, Scuseria, G. E, Robb, M. A, Cheeseman, J. R, Montgomery Jr, J. A, Vreven, T, Kudin, K. N, Burant, J. C, Millam, J. M, Iyengar, S. S, Tomasi, J, Barone, V, Mennucci, B, Cossi, M, Scalmani, G, Rega, N, Petersson, G. A, Nakatsuji, H, Hada, M, Ehara, M, Toyota, K, Fukuda, R, Hasegawa, J, Ishida, M, Nakajima, T, Honda, Y, Kitao, O, Nakai, H, Klene, M, Li, X, Knox, J. E, Hratchian, H. P, Cross, J. B, Adamo, C, Jaramillo, J, Gomperts, R, Stratmann, R. E, Yazyev, O, Austin, A. J, Cammi, R, Pomelli, C, Ochterski, J. W, Ayala, P. Y, Morokuma, K, Voth, G. A, Salvador, P, Dannenberg, J. J, Zakrzewski, V. G, Dapprich, S, Daniels, A. D, Strain, M. C, Farkas, O, Malick, D. K, Rabuck, A. D, Raghavachari, K, Foresman, J. B, Ortiz. J. V, Cui, Q, Baboul, A. G, Clifford, S, Cioslowski, J, Stefanov, B. B, Liu, G, Liashenko, A, Piskorz, P, Komaromi, I, Martin, R. L, Fox, D. J, Keith, T, Al.La
    • Frisch, M. J. ; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Montgomery Jr., J. A.; Vreven, T.; Kudin, K. N.; Burant, J. C.; Millam, J. M.; Iyengar, S. S.; Tomasi, J.; Barone, V.; Mennucci, B.; Cossi, M.; Scalmani, G.; Rega, N.; Petersson, G. A.; Nakatsuji, H.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Klene, M.; Li, X.; Knox, J. E.; Hratchian, H. P.; Cross, J. B.; Adamo, C.; Jaramillo, J.; Gomperts, R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C.; Ochterski, J. W.; Ayala, P. Y.; Morokuma, K.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Zakrzewski, V. G.; Dapprich, S.; Daniels, A. D.; Strain, M. C.; Farkas, O.; Malick, D. K.; Rabuck, A. D.; Raghavachari, K.; Foresman, J. B.; Ortiz. J. V.; Cui, Q.; Baboul, A. G.; Clifford, S.; Cioslowski, J.; Stefanov, B. B.; Liu, G.; Liashenko, A.; Piskorz, P.; Komaromi, I.; Martin, R. L.; Fox, D. J.; Keith, T.; Al.Laham, M. A.; Peng, C. Y.; Nanayakkara, A.; Challacombe, M.; Gill, P. M. W.; Johnson, B.; Chen, W.; Wong, M. W.; Gonzalez. C.; Pople, J. A. Gaussian03, Revision C.02 ed.; Gaussian, Inc., Wallingford, CT, 2004.
  • 72
    • 53849132340 scopus 로고    scopus 로고
    • While different azole and phosphines were used in the two computational studies by the Bergman-Ellman group, a preliminary comparison by us on the overall mechanism indicated the rate-determining step remains unaltered with minor modifications to the azole and phosphine ligands
    • While different azole and phosphines were used in the two computational studies by the Bergman-Ellman group, a preliminary comparison by us on the overall mechanism indicated the rate-determining step remains unaltered with minor modifications to the azole and phosphine ligands.
  • 73
    • 53849085792 scopus 로고    scopus 로고
    • M and 9 are slightly different in following transition structures L and 8, respectively; however, they are related by minor conformational twists which would be negligible under experimental conditions.
    • M and 9 are slightly different in following transition structures L and 8, respectively; however, they are related by minor conformational twists which would be negligible under experimental conditions.
  • 74
    • 53849115011 scopus 로고    scopus 로고
    • +.
    • +.
  • 75
    • 53849127139 scopus 로고    scopus 로고
    • - ion under gas-phase calculations, and use of a true noncoordinating anion under experimental conditions would considerably reduce this initial barrier.
    • - ion under gas-phase calculations, and use of a true noncoordinating anion under experimental conditions would considerably reduce this initial barrier.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.