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Volumn 20, Issue 52, 2014, Pages 17272-17276

Palladium-catalyzed α-arylation of arylketones at low catalyst loadings

Author keywords

Catalysts; Ketone arylation; Monodentate ligands; NHC; Palladium

Indexed keywords

AROMATIC COMPOUNDS; CHEMICAL REACTIONS; KETONES; LIGANDS; ORGANIC COMPOUNDS; PALLADIUM;

EID: 84920123053     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201404900     Document Type: Article
Times cited : (26)

References (57)
  • 2
    • 22844434133 scopus 로고    scopus 로고
    • Angew. Chem. 2005, 117, 4516-4563
    • (2005) Angew. Chem. , vol.117 , pp. 4516-4563
  • 6
    • 84869055480 scopus 로고    scopus 로고
    • Angew. Chem. 2012, 124, 5150-5174.
    • (2012) Angew. Chem. , vol.124 , pp. 5150-5174
  • 9
    • 84861629840 scopus 로고    scopus 로고
    • Angew. Chem. 2012, 124, 3370-3388
    • (2012) Angew. Chem. , vol.124 , pp. 3370-3388
  • 13
    • 0037393778 scopus 로고    scopus 로고
    • For exhaustive reviews covering the period until 2010, see: a)
    • For exhaustive reviews covering the period until 2010, see: a) D. A. Culkin, J. F Hartwig, Acc. Chem. Res. 2003, 36, 234-245
    • (2003) Acc. Chem. Res. , vol.36 , pp. 234-245
    • Culkin, D.A.1    Hartwig, J.F.2
  • 16
    • 77953484672 scopus 로고    scopus 로고
    • Angew. Chem. 2010, 122, 686-718
    • (2010) Angew. Chem. , vol.122 , pp. 686-718
  • 17
    • 84873304706 scopus 로고    scopus 로고
    • For a review on the complementary topic of alkenylation of ketones, see: d)
    • For a review on the complementary topic of alkenylation of ketones, see: d)T. Ankner, C. C. Cosner, P. Helquist, Chem. Eur. J. 2013, 19, 1858-1871.
    • (2013) Chem. Eur. J. , vol.19 , pp. 1858-1871
    • Ankner, T.1    Cosner, C.C.2    Helquist, P.3
  • 18
  • 30
    • 0034801556 scopus 로고    scopus 로고
    • For selected examples of arylation of other carbonyl compounds, see: a)
    • For selected examples of arylation of other carbonyl compounds, see: a) D. A. Culkin, J. F Hartwig, J. Am. Chem. Soc. 2001, 123, 5816-5817
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 5816-5817
    • Culkin, D.A.1    Hartwig, J.F.2
  • 35
    • 84871013524 scopus 로고    scopus 로고
    • For recent examples of arylation of ketones using other metals as catalyst, see: a)
    • For recent examples of arylation of ketones using other metals as catalyst, see: a)G. Danoun, A. Tlili, F Monnier, M. Taillefer, Angew. Chem. Int. Ed. 2012, 51, 12815-12819
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 12815-12819
    • Danoun, G.1    Tlili, A.2    Monnier, F.3    Taillefer, M.4
  • 36
    • 84882894009 scopus 로고    scopus 로고
    • Angew. Chem. 2012, 124, 12987-12991
    • (2012) Angew. Chem. , vol.124 , pp. 12987-12991
  • 41
    • 84884290065 scopus 로고    scopus 로고
    • Angew. Chem. 2013, 125, 7383-7387
    • (2013) Angew. Chem. , vol.125 , pp. 7383-7387
  • 42
    • 84864607963 scopus 로고    scopus 로고
    • For other examples of arylation of acetone, see: c)
    • For other examples of arylation of acetone, see: c) L. Ackermann, V. P. Mehta, Chem. Eur. J. 2012, 18, 10230-10233
    • (2012) Chem. Eur. J. , vol.18 , pp. 10230-10233
    • Ackermann, L.1    Mehta, V.P.2
  • 52
    • 76149119399 scopus 로고    scopus 로고
    • Angew. Chem. 2009, 121, 2419-2423
    • (2009) Angew. Chem. , vol.121 , pp. 2419-2423
  • 56
    • 84920134421 scopus 로고    scopus 로고
    • Compare the optimized conditions used in this work with those reported in references [5g], [6b], [8a] and [9a]. Reference [5g] also contains interesting insights into the base/solvent system
    • Compare the optimized conditions used in this work with those reported in references [5g], [6b], [8a] and [9a]. Reference [5g] also contains interesting insights into the base/solvent system.
  • 57
    • 84920145623 scopus 로고    scopus 로고
    • I. Gazic Smilovic, C. Seechurn, T. J. Colacot (LEK Pharmaceuticals Ltd.), PCT/EP2012/059236
    • I. Gazic Smilovic, C. Seechurn, T. J. Colacot (LEK Pharmaceuticals Ltd.), PCT/EP2012/059236.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.