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Volumn 18, Issue 46, 2012, Pages 14643-14648

Copper- and phosphine-ligand-free palladium-catalyzed direct allylation of electron-deficient polyfluoroarenes with allylic chlorides

Author keywords

allylic compounds; C H activation; palladium; pivalic acid; polyfluoroarenes; synthetic methods

Indexed keywords

ALLYLIC COMPOUNDS; C-H ACTIVATION; PIVALIC ACID; POLYFLUOROARENES; SYNTHETIC METHODS;

EID: 84868679055     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201202824     Document Type: Article
Times cited : (68)

References (75)
  • 7
    • 0003928002 scopus 로고
    • (Eds.: A. R. Katritzky, O. Meth-Cohn, C. W. Rees); Elsevier, New York
    • Comprehensive Organic Functional Group Transformations, (Eds.:, A. R. Katritzky, O. Meth-Cohn, C. W. Rees,); Elsevier, New York, 1995
    • (1995) Comprehensive Organic Functional Group Transformations
  • 8
    • 0003445429 scopus 로고    scopus 로고
    • (Eds.: E. N. Jacobsen, A. Pfaltz, H.Yamamoto), Springer: New York
    • Comprehensive Asymmetric Catalysis, (Eds.:, E. N. Jacobsen, A. Pfaltz, H.Yamamoto,), Springer: New York, 1999
    • (1999) Comprehensive Asymmetric Catalysis
  • 23
    • 34147109763 scopus 로고    scopus 로고
    • only one example of Lewis acid catalyzed direct intramolecular C-H allylation of moderate electron-deficient arenes has been reported, see
    • R. Hayashi, G. R. Cook, Org. Lett. 2007, 9, 1311-1314; only one example of Lewis acid catalyzed direct intramolecular C-H allylation of moderate electron-deficient arenes has been reported, see
    • (2007) Org. Lett. , vol.9 , pp. 1311-1314
    • Hayashi, R.1    Cook, G.R.2
  • 30
    • 72449170089 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 9792-9826
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9792-9826
  • 38
    • 79952655564 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 2990-2994
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 2990-2994
  • 40
    • 79959251312 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 5918-5923
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 5918-5923
  • 42
    • 84859965961 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2012, 51, 4122-4127.
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 4122-4127
  • 44
  • 69
    • 78449297553 scopus 로고    scopus 로고
    • for other examples, see
    • D. Lapointe, K. Fagnou, Chem. Lett. 2010, 39, 1118-1126; for other examples, see
    • (2010) Chem. Lett. , vol.39 , pp. 1118-1126
    • Lapointe, D.1    Fagnou, K.2
  • 74
    • 84858776560 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2012, 51, 3066-3072.
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 3066-3072
  • 75
    • 0000347169 scopus 로고
    • The (π-allyl)palladium acetate II-1 was prepared according to the literature, see.
    • The (π-allyl)palladium acetate II-1 was prepared according to the literature, see:, S. D. Robinson, B. L. Shaw, J. Organomet. Chem. 1965, 3, 367.
    • (1965) J. Organomet. Chem. , vol.3 , pp. 367
    • Robinson, S.D.1    Shaw, B.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.