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Volumn 16, Issue 22, 2014, Pages 5934-5936

A facile access to 4-substituted-2-naphthols via a tandem Friedel-Crafts reaction: A β-chlorovinyl ketone pathway

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EID: 84912550709     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol502951v     Document Type: Article
Times cited : (45)

References (23)
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    • Pu, L. Chem. Rev. 1998, 98, 2405
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    • Pu, L. Chem. Rev. 2004, 104, 1687
    • (2004) Chem. Rev. , vol.104 , pp. 1687
    • Pu, L.1
  • 13
    • 0001652150 scopus 로고
    • For the selectivity issue of naphthalene, see
    • For the selectivity issue of naphthalene, see: Olah, G. A.; Olah, J. A. J. Am. Chem. Soc. 1976, 98, 1839
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 1839
    • Olah, G.A.1    Olah, J.A.2
  • 20
    • 20344375712 scopus 로고    scopus 로고
    • Our effort to isolate β-chlorovinyl ketone intermediates from the reaction of trimethylsilyl acetylene was not successful. Previously, Juteau and coworkers at Merck Frost Canada reported the synthesis of 3-(triisopropylsilyl)-2-naphthols under similar reaction conditions using triisopropylsilyl acetylene; see
    • Our effort to isolate β-chlorovinyl ketone intermediates from the reaction of trimethylsilyl acetylene was not successful. Previously, Juteau and coworkers at Merck Frost Canada reported the synthesis of 3-(triisopropylsilyl)-2-naphthols under similar reaction conditions using triisopropylsilyl acetylene; see: Juteau, H.; Gareau, Y.; Lachance, H. Tetrahedron Lett. 2005, 46, 4547
    • (2005) Tetrahedron Lett. , vol.46 , pp. 4547
    • Juteau, H.1    Gareau, Y.2    Lachance, H.3
  • 21
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    • The greater stability of the vinylic cation by a phenyl rather than an alkyl group has been invoked; see
    • The greater stability of the vinylic cation by a phenyl rather than an alkyl group has been invoked; see: Martens, H.; Janssens, F.; Hoornaert, G. Tetrahedron 1975, 31, 177
    • (1975) Tetrahedron , vol.31 , pp. 177
    • Martens, H.1    Janssens, F.2    Hoornaert, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.