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Volumn 129, Issue 46, 2007, Pages 14190-14192

Copper(I)-α-ketocarboxylate complexes: Characterization and O 2 reactions that yield copper-oxygen intermediates capable of hydroxylating arenes

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLIC ACID DERIVATIVE; COPPER; COPPER COMPLEX; KETONE DERIVATIVE; OXYGEN; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE;

EID: 36448976584     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0760426     Document Type: Article
Times cited : (85)

References (55)
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    • + acting as the oxidant in this enzyme are summarized in ref 4d and the following: Klinman, J. P. J. Biol. Chem. 2006, 281, 3013-3016.
    • + acting as the oxidant in this enzyme are summarized in ref 4d and the following: Klinman, J. P. J. Biol. Chem. 2006, 281, 3013-3016.
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    • For example, see: a, Jr
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    • (2007) Acc. Chem. Res , vol.40 , pp. 493-500
    • Que, L.1
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    • (c) Nam, W. Acc. Chem. Res. 2007, 40, 522-531.
    • (2007) Acc. Chem. Res , vol.40 , pp. 522-531
    • Nam, W.1
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    • Examples of related arene substituent hydroxylations using mononuclear complexes have been reported. For cases proposed to involve a [CuO, intermediate, see refs 7c and d, and for examples involving other types of intermediates, see: (a) Kunishita, A, Teraoka, J, Scanlon, J. D, Matsumoto, T, Suzuki, M, Cramer, C. J, Itoh, S. J. Am. Chem. Soc. 2007, 129, 7248-7249
    • + intermediate, see refs 7c and d, and for examples involving other types of intermediates, see: (a) Kunishita, A.; Teraoka, J.; Scanlon, J. D.; Matsumoto, T.; Suzuki, M.; Cramer, C. J.; Itoh, S. J. Am. Chem. Soc. 2007, 129, 7248-7249.
  • 46
    • 33744786786 scopus 로고    scopus 로고
    • For a copper(II)-promoted ortho-hydroxylation of 2-phenylpyridine proposed to involve a single electron transfer mechanism, see: Chen, X.; Hao, X. S.; Goodhue, C. E.; Yu, J. Q. J. Am. Chem. Soc. 2006, 128, 6790-6791.
    • For a copper(II)-promoted ortho-hydroxylation of 2-phenylpyridine proposed to involve a single electron transfer mechanism, see: Chen, X.; Hao, X. S.; Goodhue, C. E.; Yu, J. Q. J. Am. Chem. Soc. 2006, 128, 6790-6791.
  • 47
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    • For details, see Supporting Information
    • For details, see Supporting Information.
  • 51
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    • M06L: Zhao, Y, Truhlar, D. G. J. Chem. Phys. 2006, 125, 194101
    • (a) M06L: Zhao, Y.; Truhlar, D. G. J. Chem. Phys. 2006, 125, 194101.
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    • CASPT2: Andersson, K.; Malmqvist, P.-Å.; Roos, B. O. J. Chem. Phys. 1992, 96, 1218-1226.
    • (b) CASPT2: Andersson, K.; Malmqvist, P.-Å.; Roos, B. O. J. Chem. Phys. 1992, 96, 1218-1226.
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    • See Supporting Information for additional details and references
    • (c) See Supporting Information for additional details and references.
  • 54
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    • 2 is unlikely to be involved in the process(es) that yield(s) hydroxylated ligand.
    • 2 is unlikely to be involved in the process(es) that yield(s) hydroxylated ligand.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.