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Volumn 13, Issue 7, 2011, Pages 1652-1654

Connecting the dots: Using sunlight to drive electrochemical oxidations

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EID: 79960234311     PISSN: 14639262     EISSN: 14639270     Source Type: Journal    
DOI: 10.1039/c1gc15207f     Document Type: Article
Times cited : (26)

References (27)
  • 1
    • 0012413765 scopus 로고    scopus 로고
    • For an extensive review of electrochemical reactions in synthesis, see: H. Lund, O. Hammerich, ed.; Dekker, New York
    • For an extensive review of electrochemical reactions in synthesis, see: Organic Electrochemistry: Fourth Edition, Revised and Expanded, H. Lund, O. Hammerich, ed.; Dekker, New York, 2001.
    • (2001) Organic Electrochemistry: Fourth Edition, Revised and Expanded
  • 2
    • 0003870190 scopus 로고
    • For the basics of electrochemical oxidation reactions, see: Wiley-Interscience, New York
    • For the basics of electrochemical oxidation reactions, see: K. Yoshida Electrooxidation in Organic Chemistry, Wiley-Interscience, New York, 1984.
    • (1984) Electrooxidation in Organic Chemistry
    • Yoshida, K.1
  • 5
    • 78049392925 scopus 로고    scopus 로고
    • For an alternative chemical approach using oxygen as a co-oxidant, see: references therein
    • For an alternative chemical approach using oxygen as a co-oxidant, see: A. N. Campbell P. B. White I. A. Guzei S. S. Stahl J. Am. Chem. Soc. 2010 132 15116, and references therein.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 15116
    • Campbell, A.N.1    White, P.B.2    Guzei, I.A.3    Stahl, S.S.4
  • 12
    • 38349133540 scopus 로고    scopus 로고
    • H. J. Schäfer, ed.; Wiley-VCH, Weinheim Germany, chapter 15
    • S. Torii, Organic Electrochemistry, H. J. Schäfer, ed.; Wiley-VCH, Weinheim Germany, 2004, chapter 15, p. 503.
    • (2004) Organic Electrochemistry , pp. 503
    • Torii, S.1
  • 21
    • 85032757134 scopus 로고    scopus 로고
    • The photovoltaic-cells employed in these experiments are available from Solar-Made
    • The photovoltaic-cells employed in these experiments are available from Solar-Made.
  • 24
    • 0030580377 scopus 로고    scopus 로고
    • For an example of a carbamate oxidation being more difficult than an enol ether oxidation please, see
    • For an example of a carbamate oxidation being more difficult than an enol ether oxidation please, see: D. A. Frey N. Wu K. D. Moeller Tetrahedron Lett. 1996 37 8317.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 8317
    • Frey, D.A.1    Wu, N.2    Moeller, K.D.3
  • 25
    • 0001503281 scopus 로고    scopus 로고
    • For the preparative oxidation of 8 using the traditional setup, see
    • For the preparative oxidation of 8 using the traditional setup, see: Y. M. Fobian K. D. Moeller Methods Mol. Med. 1999 23 259.
    • (1999) Methods Mol. Med. , vol.23 , pp. 259
    • Fobian, Y.M.1    Moeller, K.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.