메뉴 건너뛰기




Volumn 18, Issue 7, 2012, Pages 2113-2122

Electrophilic arene hydroxylation and phenol O-H oxidations performed by an unsymmetric μ-η1:η1-O 2-peroxo dicopper(II) complex

Author keywords

coordination modes; electron transfer; hydroxylation; reaction mechanisms; reactive intermediates

Indexed keywords

ASSOCIATION REACTIONS; BINDING ENERGY; COPPER COMPOUNDS; ELECTRON TRANSITIONS; FREE RADICAL REACTIONS; GROUND STATE; HYDROXYLATION; MECHANICS; OXIDATION; PEROXIDES; PHENOLS; REACTION INTERMEDIATES; SPECTROSCOPIC ANALYSIS;

EID: 84856707068     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201102372     Document Type: Article
Times cited : (26)

References (64)
  • 2
    • 0035905357 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2001, 40, 4570-4590.
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 4570-4590
  • 6
    • 3242801689 scopus 로고    scopus 로고
    • (Eds.: J. A. McCleverty, T. J. Meyer), Elsevier
    • S. Itoh, in Dicopper Enzymes, Vol. 8 (Eds.:, J. A. McCleverty, T. J. Meyer,), Elsevier, 2003, 369-393.
    • (2003) Dicopper Enzymes , vol.8 , pp. 369-393
    • Itoh, S.1
  • 17
    • 33746291588 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 4546-4550.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 4546-4550
  • 21
    • 0034595323 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 1591-1595.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 1591-1595
  • 44
    • 77953533256 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 2406-2409.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 2406-2409
  • 46
    • 77956037499 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 6438-6442.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 6438-6442


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.