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Volumn 9, Issue 21, 2007, Pages 4299-4302

Gold-catalyzed etherification and friedel - Crafts alkylation using ortho-alkynylbenzoic acid alkyl ester as an efficient alkylating agent

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EID: 35548937481     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol701861d     Document Type: Article
Times cited : (65)

References (59)
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    • For reviews, see:, Yamamoto, H, Ed, Wiley-VCH: Weinheim, Germany, Vols
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  • 2
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    • For recent reviews on the Au-catalyzed reactions, see: a
    • For recent reviews on the Au-catalyzed reactions, see: (a) Hoffmann-Röder, A.; Krause, N. Org. Biomol. Chem. 2005, 3, 387.
    • (2005) Org. Biomol. Chem , vol.3 , pp. 387
    • Hoffmann-Röder, A.1    Krause, N.2
  • 12
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    • 0011196413 scopus 로고    scopus 로고
    • Electrocyclization of ortho-alkynylbenzoic acid alkyl ester has been reported for synthesis of isocoumarin. For examples, see: (a) Oliver, M. A, Gandour, R. D. J. Org. Chem. 1984, 49, 558
    • Electrocyclization of ortho-alkynylbenzoic acid alkyl ester has been reported for synthesis of isocoumarin. For examples, see: (a) Oliver, M. A.; Gandour, R. D. J. Org. Chem. 1984, 49, 558.
  • 16
    • 27544467800 scopus 로고    scopus 로고
    • 2-catalyzed cyclization of benzoic acid ester through carboalkoxylation of the alkyne has been reported; see: Fürstner, A.; Davies, P. W. J. Am. Chem. Soc. 2005, 127, 15024.
    • 2-catalyzed cyclization of benzoic acid ester through carboalkoxylation of the alkyne has been reported; see: Fürstner, A.; Davies, P. W. J. Am. Chem. Soc. 2005, 127, 15024.
  • 17
    • 27544457189 scopus 로고    scopus 로고
    • For recent other examples of metal-catalyzed intramolecular carboalkoxylation of alkynes, see: a
    • For recent other examples of metal-catalyzed intramolecular carboalkoxylation of alkynes, see: (a) Nakamura, I.; Mizushima, Y.; Yamamoto, Y. J. Am. Chem. Soc. 2005, 127, 15022.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 15022
    • Nakamura, I.1    Mizushima, Y.2    Yamamoto, Y.3
  • 19
    • 0000873705 scopus 로고    scopus 로고
    • For examples of catalytic etherifications, see: (a) Kashman, Y. J. Org. Chem. 1972, 37, 912
    • For examples of catalytic etherifications, see: (a) Kashman, Y. J. Org. Chem. 1972, 37, 912.
  • 31
    • 0034623551 scopus 로고    scopus 로고
    • For examples of metal-catalyzed dehydration of alcohols, see: (a) Nishibayashi, Y, Wakiji, I, Hidai, M. J. Am. Chem. Soc. 2000, 122, 11019
    • For examples of metal-catalyzed dehydration of alcohols, see: (a) Nishibayashi, Y.; Wakiji, I.; Hidai, M. J. Am. Chem. Soc. 2000, 122, 11019.
  • 37
    • 0042379988 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Trost, B. M.; Crawley, M. L. Chem. Rev. 2003, 103, 2921.
    • (2003) Chem. Rev , vol.103 , pp. 2921
    • Trost, B.M.1    Crawley, M.L.2
  • 47
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    • For selected examples of transition-metal-catalyzed Friedel-Crafts alkylations, see: a
    • For selected examples of transition-metal-catalyzed Friedel-Crafts alkylations, see: (a) Malkov, A. V.; Davis, S. L.; Baxendale, I. R.; Mitchell, W. L.; Koc̀ovský, P. J. Org. Chem 1999, 64, 2751.
    • (1999) J. Org. Chem , vol.64 , pp. 2751
    • Malkov, A.V.1    Davis, S.L.2    Baxendale, I.R.3    Mitchell, W.L.4    Koc̀ovský, P.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.