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Volumn 132, Issue 41, 2010, Pages 14682-14687

Oxidation of a cyclometalated Pd(II) dimer with "cF3 +": Formation and reactivity of a catalytically competent monomeric Pd(IV) aquo complex

Author keywords

[No Author keywords available]

Indexed keywords

BENZO[H]QUINOLINE; BOND FORMATION; BOND FORMING; CHEMOSELECTIVE; LEWIS ACIDIC; NUCLEARITY; REDUCTIVE ELIMINATION; TRIFLUOROMETHYLATION;

EID: 77958047714     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja107780w     Document Type: Article
Times cited : (215)

References (73)
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    • IV complexes, see
    • IV complexes, see
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    • 77958067657 scopus 로고    scopus 로고
    • 2H-promoted Pd-catalyzed C-H trifluoromethylation that appeared while this work was in progress, see
    • 2H-promoted Pd-catalyzed C-H trifluoromethylation that appeared while this work was in progress, see
  • 20
    • 77958068538 scopus 로고    scopus 로고
    • For examples of other Pd-catalyzed C-H functionalization reactions in which Brønsted/Lewis acids are used as additives/promoters, see
    • For examples of other Pd-catalyzed C-H functionalization reactions in which Brønsted/Lewis acids are used as additives/promoters, see
  • 25
  • 28
    • 77958072235 scopus 로고    scopus 로고
    • 4 led to nearly identical yields of 6
    • 4 led to nearly identical yields of 6.
  • 29
    • 77958040867 scopus 로고    scopus 로고
    • +" (from 0.5-3) used in this reaction. Lower equivalents of oxidant simply led to lower % conversion of 3. See the Supporting Information (Table S3) for details
    • +" (from 0.5-3) used in this reaction. Lower equivalents of oxidant simply led to lower % conversion of 3. See the Supporting Information (Table S3) for details.
  • 30
    • 77958056981 scopus 로고    scopus 로고
    • Hydrogen atoms were placed in idealized positions with the exception of those of the H-bonded waters, which were allowed to refine isotropically with a restrained O-H distance and common U (iso)
    • Hydrogen atoms were placed in idealized positions with the exception of those of the H-bonded waters, which were allowed to refine isotropically with a restrained O-H distance and common U (iso).
  • 34
    • 77958062726 scopus 로고    scopus 로고
    • For other examples of C-O bond-forming reductive elimination, see
    • For other examples of C-O bond-forming reductive elimination, see
  • 44
    • 77958032966 scopus 로고    scopus 로고
    • 3 bond formation at Cu/Ni, see
    • 3 bond formation at Cu/Ni, see
  • 48
    • 77958032687 scopus 로고    scopus 로고
    • 2 as the major inorganic products. See the Supporting Information for full details
    • 2 as the major inorganic products. See the Supporting Information for full details.
  • 49
    • 77958033262 scopus 로고    scopus 로고
    • For examples, see
    • For examples, see
  • 50
    • 77958059280 scopus 로고    scopus 로고
    • Reference 5a
    • Reference 5a.
  • 51
    • 77958054090 scopus 로고    scopus 로고
    • Reference 7
    • Reference 7.
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    • 77958049288 scopus 로고    scopus 로고
    • IV, see
    • IV, see
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    • 77958063296 scopus 로고    scopus 로고
    • Reference 5b
    • Reference 5b.
  • 58
    • 77958032365 scopus 로고    scopus 로고
    • IV, see
    • IV, see
  • 61
    • 77958063887 scopus 로고    scopus 로고
    • Reference 17c
    • Reference 17c.
  • 65
    • 77958035599 scopus 로고    scopus 로고
    • Reference 17e
    • Reference 17e.
  • 67
    • 77958073129 scopus 로고    scopus 로고
    • IV, see
    • IV, see
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    • 77958028133 scopus 로고    scopus 로고
    • IV, see
    • IV, see
  • 73
    • 77958033537 scopus 로고    scopus 로고
    • Reference 5b
    • Reference 5b.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.