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Volumn 6, Issue 6, 2015, Pages 3410-3414

Nickel-catalyzed reductive cleavage of aryl alkyl ethers to arenes in absence of external reductant

Author keywords

[No Author keywords available]

Indexed keywords

ATOMS; HYDROGEN; KETONES; NICKEL; SELECTIVE CATALYTIC REDUCTION; SYNTHESIS (CHEMICAL);

EID: 84929600571     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c5sc00305a     Document Type: Article
Times cited : (92)

References (46)
  • 21
    • 80052844225 scopus 로고    scopus 로고
    • Selected works on reductive cleavage of aryl ethers under heterogeneous catalysis
    • M. Tobisu N. Chatani ChemCatChem 2011 3 1410
    • (2011) ChemCatChem , vol.3 , pp. 1410
    • Tobisu, M.1    Chatani, N.2
  • 41
    • 84919608256 scopus 로고    scopus 로고
    • see also ref. 6a, b and d In fact, stoichiometric studies by Martin (ref. 6d) reported successful isolation of an acetaldehyde-bound nickel(0) complex, while the attempted synthesis of the corresponding formaldehyde complex resulted in the formation of a carbonyl-nickel(0) complex via a rapid decarbonylation process
    • E. Koch R. Takise A. Studer J. Yamaguchi K. Itami Chem. Commun. 2015 51 855
    • (2015) Chem. Commun. , vol.51 , pp. 855
    • Koch, E.1    Takise, R.2    Studer, A.3    Yamaguchi, J.4    Itami, K.5
  • 43
    • 75649103176 scopus 로고    scopus 로고
    • Selected examples for the importance of the flexibility of the NHC ligands
    • H. Clavier S. P. Nolan Chem. Commun. 2010 46 841
    • (2010) Chem. Commun. , vol.46 , pp. 841
    • Clavier, H.1    Nolan, S.P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.