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Volumn 21, Issue 4, 2015, Pages 1790-1794

Ruthenium(II)-Catalyzed CH acyloxylation of phenols with removable auxiliary

Author keywords

Benzoic acids; CH activation; Phenols; Reaction mechanisms; Ruthenium

Indexed keywords

BENZOIC ACID; CATALYSTS; CHEMICAL ACTIVATION; FUNCTIONAL GROUPS; PHENOLS; RUTHENIUM; SUBSTRATES;

EID: 84920982982     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201405071     Document Type: Article
Times cited : (62)

References (77)
  • 1
    • 84920996512 scopus 로고    scopus 로고
    • For selected representative recent reviews on CH activation, see
    • For selected representative recent reviews on CH activation, see:
  • 7
    • 84871962677 scopus 로고    scopus 로고
    • Angew. Chem. 2012, 124, 9092-9142
    • (2012) Angew. Chem. , vol.124 , pp. 9092-9142
  • 11
    • 77949410036 scopus 로고    scopus 로고
    • Angew. Chem. 2009, 121, 9976-10011
    • (2009) Angew. Chem. , vol.121 , pp. 9976-10011
  • 15
    • 80054999158 scopus 로고    scopus 로고
    • For a recent review, see: and references therein
    • For a recent review, see: S. Enthaler, A. Company, Chem. Soc. Rev. 2011, 40, 4912-4924, and references therein.
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 4912-4924
  • 16
    • 84920996511 scopus 로고    scopus 로고
    • For selected examples of catalyzed direct acyloxylations with metals other than ruthenium, see
    • For selected examples of catalyzed direct acyloxylations with metals other than ruthenium, see:
  • 27
    • 84874599469 scopus 로고    scopus 로고
    • For general reviews on ruthenium(II)-catalyzed CH functionalization, see: S. I. Kozhushkov, L. Ackermann
    • For general reviews on ruthenium(II)-catalyzed CH functionalization, see: S. I. Kozhushkov, L. Ackermann, Chem. Sci. 2013, 4, 886-896
    • (2013) Chem. Sci. , vol.4 , pp. 886-896
  • 30
    • 77954079515 scopus 로고    scopus 로고
    • and references cited therein
    • L. Ackermann, R. Vicente, Top. Curr. Chem. 2010, 292, 211-229, and references cited therein
    • (2010) Top. Curr. Chem. , vol.292 , pp. 211-229
    • Ackermann, L.1    Vicente, R.2
  • 31
    • 84899652017 scopus 로고    scopus 로고
    • For selected examples of oxidative ruthenium(II)-catalyzed CH activation with alkenes or alkynes, see: S. Nakanowatari, L. Ackermann
    • for selected examples of oxidative ruthenium(II)-catalyzed CH activation with alkenes or alkynes, see: S. Nakanowatari, L. Ackermann, Chem. Eur. J. 2014, 20, 5409-5413
    • (2014) Chem. Eur. J. , vol.20 , pp. 5409-5413
  • 40
    • 84884836834 scopus 로고    scopus 로고
    • Angew. Chem. 2013, 125, 6813-6816
    • (2013) Angew. Chem. , vol.125 , pp. 6813-6816
  • 52
    • 80054885949 scopus 로고    scopus 로고
    • and references cited therein
    • Angew. Chem. 2011, 123, 6503 -6506, and references cited therein.
    • (2011) Angew. Chem. , vol.123 , pp. 6503-6506
  • 66
    • 84906259545 scopus 로고    scopus 로고
    • For a review, see
    • For a review, see: F. Zhang, D. R. Spring, Chem. Soc. Rev. 2014, 43, 6906-6919.
    • (2014) Chem. Soc. Rev. , vol.43 , pp. 6906-6919
  • 71
    • 84920996510 scopus 로고    scopus 로고
    • Under otherwise identical reaction conditions, equimolar amounts of the substrates 1a and 2a led to the isolation of product 3aa in 44% yield
    • Under otherwise identical reaction conditions, equimolar amounts of the substrates 1a and 2a led to the isolation of product 3aa in 44% yield.
  • 72
    • 84920996509 scopus 로고    scopus 로고
    • Additionally, a meta-methoxy-substituted arene provided the desired product also with excellent regioselectivity.
    • Additionally, a meta-methoxy-substituted arene provided the desired product also with excellent regioselectivity.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.