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Volumn 127, Issue 44, 2005, Pages 15360-15361

Exogenous nitrile substrate hydroxylation by a new dicopper-hydroperoxide complex

Author keywords

[No Author keywords available]

Indexed keywords

COPPER COMPLEX; HYDROPEROXIDE; MU 1,1 HYDROPEROXODICOPPER COMPLEX; NITRILE; UNCLASSIFIED DRUG;

EID: 27644557896     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja054948a     Document Type: Article
Times cited : (41)

References (32)
  • 1
    • 27644586991 scopus 로고    scopus 로고
    • note
    • Tyr: tyrosinase; p-MMO: particulate-methane monooxygenase; DβM: dopamine β-monooxygenase; PHM: peptidylglycine α-hydroxylating monooxygenase.
  • 18
    • 27644553730 scopus 로고    scopus 로고
    • note
    • See Supporting Information.
  • 24
    • 27644454562 scopus 로고    scopus 로고
    • note
    • -OOH orbitals with the Cu LUMO likely due to geometric constraints and the lack of hydrogen bonding for this ligand system.
  • 25
    • 27644494609 scopus 로고    scopus 로고
    • note
    • 9b
  • 26
    • 27644476482 scopus 로고    scopus 로고
    • note
    • 9c
  • 27
  • 30
    • 27644465102 scopus 로고    scopus 로고
    • note
    • Material balance is overall excellent: When 2 is warmed from -80 °C, a ligand arm oxidative dehydrogenation (∼60% yield) and autoxidation occur, the latter giving a hydroxo-bridged tetranuclear cluster (≤25% yield). These results will be described elsewhere.
  • 31
    • 27644455436 scopus 로고    scopus 로고
    • note
    • 2CN solvent peak. Thus, if mandelonitrile is simultaneously produced in the nitrile oxidation reaction, our estimate for the overall yield of the process is low.
  • 32
    • 27644511826 scopus 로고    scopus 로고
    • note
    • 16 due to their favorable proximity.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.