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Volumn 49, Issue 41, 2008, Pages 6013-6015

Selective aromatic carbon-oxygen bond cleavage of trifluoromethoxyarenes: a trifluoromethoxy group as a convertible directing group

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUND; CHLOROTRIMETHYLSILANE; SILANE; SODIUM; TRIFLUOROMETHOXYARENE; UNCLASSIFIED DRUG;

EID: 50049108867     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.08.002     Document Type: Article
Times cited : (16)

References (54)
  • 1
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    • Activation of C-O Bonds: Stoichiometric and Catalytic Reactions
    • Murai S. (Ed), Springer, Berlin
    • Lin Y.-S., and Yamamoto A. Activation of C-O Bonds: Stoichiometric and Catalytic Reactions. In: Murai S. (Ed). Activation of Unreactive Bonds and Organic Synthesis (1999), Springer, Berlin 161-192
    • (1999) Activation of Unreactive Bonds and Organic Synthesis , pp. 161-192
    • Lin, Y.-S.1    Yamamoto, A.2
  • 31
    • 50049123474 scopus 로고    scopus 로고
    • note
    • 18Si: C, 75.71; H, 9.53. Found: C, 75.72; H, 9.77.
  • 32
    • 34548061498 scopus 로고    scopus 로고
    • 3 was detected. Probably, decomposition of the metal trifluoromethoxide took place. See:
    • 3 was detected. Probably, decomposition of the metal trifluoromethoxide took place. See:. Christe K.O., Hegge J., Hoge B., and Haiges R. Angew. Chem., Int. Ed. 46 (2007) 6155-6158
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 6155-6158
    • Christe, K.O.1    Hegge, J.2    Hoge, B.3    Haiges, R.4
  • 33
    • 0348208897 scopus 로고
    • Selected examples of electroreductive syntheses of organosilicon compounds:
    • Selected examples of electroreductive syntheses of organosilicon compounds:. Yoshida J., Muraki K., Funahashi H., and Kawabata N. J. Organomet. Chem. 284 (1985) C33-C35
    • (1985) J. Organomet. Chem. , vol.284
    • Yoshida, J.1    Muraki, K.2    Funahashi, H.3    Kawabata, N.4
  • 40
    • 0037970037 scopus 로고    scopus 로고
    • Organoalkali Chemistry
    • Schlosser M. (Ed), Wiley, Chichester Chapter 1, pp 1-352
    • Schlosser M. Organoalkali Chemistry. In: Schlosser M. (Ed). Organometallics in Synthesis: A Manual, 2nd ed. (2002), Wiley, Chichester Chapter 1, pp 1-352
    • (2002) Organometallics in Synthesis: A Manual, 2nd ed.
    • Schlosser, M.1
  • 41
    • 0346265937 scopus 로고
    • Abel E.W., Stone F.G.A., and Wilkinson G. (Eds), Pergamon, New York Chapter 1, pp 1-92
    • Gray M., Tinkl M., and Snieckus V. In: Abel E.W., Stone F.G.A., and Wilkinson G. (Eds). Comprehensive Organometallic Chemistry II Vol. 11 (1995), Pergamon, New York Chapter 1, pp 1-92
    • (1995) Comprehensive Organometallic Chemistry II , vol.11
    • Gray, M.1    Tinkl, M.2    Snieckus, V.3
  • 44
    • 33947378268 scopus 로고    scopus 로고
    • As an example including the concept of convertible directing groups, Yoshida et al. reported the generation and reactions of o-bromophenyllithium without benzyne formation using a microreactor:
    • As an example including the concept of convertible directing groups, Yoshida et al. reported the generation and reactions of o-bromophenyllithium without benzyne formation using a microreactor:. Usutani H., Tomida Y., Nagaki A., Okamoto H., Nokami T., Yoshida J. J. Am. Chem. Soc. 129 (2007) 3046-3047
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 3046-3047
    • Usutani, H.1    Tomida, Y.2    Nagaki, A.3    Okamoto, H.4    Nokami, T.5    Yoshida, J.6
  • 45
    • 0004394843 scopus 로고
    • Sulfoxide-based convertible directing groups:
    • Sulfoxide-based convertible directing groups:. Ogawa S., and Furukawa N. J. Org. Chem. 56 (1991) 5723-5726
    • (1991) J. Org. Chem. , vol.56 , pp. 5723-5726
    • Ogawa, S.1    Furukawa, N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.