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Volumn , Issue 31, 2006, Pages 3352-3354

BiCl3-catalyzed propargylic substitution reaction of propargylic alcohols with C-, O-, S- and N-centered nucleophiles

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; ALLYL COMPOUND; BISMUTH DERIVATIVE; CARBON; NITROGEN; OXYGEN; SILANE DERIVATIVE; SULFUR; TRIMETHYLSILYL DERIVATIVE;

EID: 33746709483     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b606470a     Document Type: Article
Times cited : (150)

References (33)
  • 16
    • 0037055054 scopus 로고    scopus 로고
    • The ruthenium-catalyzed propargylic substitution was reported to run via allenylidene complex intermediates which can be produced only from propargylic alcohols bearing a terminal alkyne group, see ref. 4; on the other hand, ruthenium-catalyzed substitution of propargylic alcohols bearing an internal alkyne group were also investigated, see:
    • Y. Nishibayashi Y. Inada M. Hidai S. Uemura J. Am. Chem. Soc. 2002 124 7900
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 7900
    • Nishibayashi, Y.1    Inada, Y.2    Hidai, M.3    Uemura, S.4
  • 25
    • 0006195697 scopus 로고    scopus 로고
    • The significant characteristic feature of this reaction is the direct use of propargylic alcohols as the substrates. For nucleophilic substitution of propargylic esters, see:
    • M. Postel E. Dunach Coord. Chem. Rev. 1996 155 127
    • (1996) Coord. Chem. Rev. , vol.155 , pp. 127
    • Postel, M.1    Dunach, E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.