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Volumn 51, Issue 52, 2012, Pages 13075-13079

Erratum: Synthesis of ortho-Acylphenols through the Palladium-Catalyzed Ketone-Directed Hydroxylation of Arenes (Angewandte Chemie - International Edition (2012) 51 DOI: 10.1002/anie.201207479);Synthesis of ortho-acylphenols through the palladium-catalyzed ketone-directed hydroxylation of arenes

Author keywords

C H activation; Homogeneous catalysis; Ketones; Oxidation; Palladium; homogeneous catalysis; ketones; oxidation; palladium

Indexed keywords

ACTIVATION ANALYSIS; ACYLATION; AGRICULTURAL CHEMICALS; KETONES; OXIDATION; PALLADIUM; PHENOLS;

EID: 84871980405     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201303140     Document Type: Erratum
Times cited : (185)

References (78)
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    • and references therein
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    • Although the anionic Fries rearrangement is ortho-selective, it requires strong bases (such as organolithium), and enolizable ketones are generally not tolerated, see also Ref. [6]
    • Although the anionic Fries rearrangement is ortho-selective, it requires strong bases (such as organolithium), and enolizable ketones are generally not tolerated, see also Ref. [6].
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    • For a seminal report on Cu-mediated ortho-hydroxylation of 2-arylpyridines
    • For a seminal report on Cu-mediated ortho-hydroxylation of 2-arylpyridines, see: X. Chen, X.-S. Hao, C. E. Goodhue, J.-Q. Yu, J. Am. Chem. Soc. 2006, 128, 6790.
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    • Chen, X.1    Hao, X.-S.2    Goodhue, C.E.3    Yu, J.-Q.4
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    • This is likely due to stronger Pd-Cl bonds, thus Cl ligands slowly exchange with trifluoroacetate anions
    • This is likely due to stronger Pd-Cl bonds, thus Cl ligands slowly exchange with trifluoroacetate anions.
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    • CCDC 897814 (3) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 897814 (3) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www. ccdc.cam.ac.uk/data-request/cif.
  • 74
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    • For An Example Of Similar KIEs Observed On The Activation Of Aryl C-H Bonds See: Ref. [18a]
    • For an example of similar KIEs observed on the activation of aryl C-H bonds, see: Ref. [18a].
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    • For some remarkable recent examples of Pd-catalyzed carboxylation of arenes under mild conditions by C-H activation and Ref [17]
    • For some remarkable recent examples of Pd-catalyzed carboxylation of arenes under mild conditions by C-H activation, see: R. Giri, J. K. Lam, J.-Q. Yu, J. Am. Chem. Soc. 2010, 132, 686 and Ref. [17].
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 686
    • Giri, R.1    Lam, J.K.2    Yu, J.-Q.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.