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Volumn 4, Issue 14, 2002, Pages 2285-2288

Palladium-catalyzed homocoupling reactions between two Csp3-Csp3 centers

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ARTICLE;

EID: 0000429681     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0258536     Document Type: Article
Times cited : (51)

References (29)
  • 5
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    • Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon: Oxford, U.K.
    • (e) Farina, V. Comprehensive Organometallic Chemistry II; Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon: Oxford, U.K., 1995; Vol. 12, pp 161-240.
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 161-240
    • Farina, V.1
  • 6
    • 0000617110 scopus 로고
    • Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon: Oxford, U.K.
    • (f) Leong, W. W.; Larock, R. C. In Comprehensive Organometallic Chemistry II; Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon: Oxford, U.K., 1995; Vol. 12, pp 131-160.
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 131-160
    • Leong, W.W.1    Larock, R.C.2
  • 7
    • 0001603937 scopus 로고
    • Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon: Oxford, U.K.
    • (g) Grigg, R.; Sridharan, V. Comprehensive Organometallic Chemistry II; Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon: Oxford, U.K., 1995; Vol. 12, pp 299-321.
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 299-321
    • Grigg, R.1    Sridharan, V.2
  • 15
    • 0345404157 scopus 로고    scopus 로고
    • (e) Giovannini, R.; Stüdemann, T.; Dussin, G.; Knochel, P. Angew. Chem. 1998, 110, 2512-2515. Angew. Chem., Int. Ed. 1998, 37, 2387-2390.
    • (1998) Angew. Chem., Int. Ed. , vol.37 , pp. 2387-2390
  • 17
    • 0001017531 scopus 로고
    • (f) Devasagayaraj, A.; Stüdemann, T.; Knochel, P. Angew. Chem. 1995, 107, 2952-2954; Angew. Chem., Int. Ed. Engl. 1995, 34, 2723-2725.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 2723-2725
  • 29
    • 0042498225 scopus 로고    scopus 로고
    • 602-ORGN
    • We observed the reductive elimination of an alkyl-Pd-X (X = halide) to form an alkyl-X species in high selectivity. We did not detect any arylation product from the reductive elimination of an alkyl-Pd-enolate. This leads us to believe that an alkyl-Pd-enolate intermediate was not formed in this reaction. A. Lei, X. Zhang, Abstr. Pap. Am. Chem. Soc. 2001, 222, 602-ORGN.
    • (2001) Abstr. Pap. Am. Chem. Soc. , pp. 222
    • Lei, A.1    Zhang, X.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.