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Volumn 65, Issue 9, 2009, Pages 1758-1766

Gold(III)-catalyzed direct nucleophilic substitution of propargylic alcohols

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; ALLYL COMPOUND; AROMATIC COMPOUND; BENZYL ALCOHOL; CARBONYL DERIVATIVE; DICHLOROMETHANE; GOLD; NUCLEOPHILE; SILANE DERIVATIVE; SULFONAMIDE; THIOL DERIVATIVE;

EID: 58949100680     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.12.051     Document Type: Article
Times cited : (132)

References (72)
  • 6
    • 58949098553 scopus 로고    scopus 로고
    • Very recently asymmetric versions of this reaction have been described:
    • Very recently asymmetric versions of this reaction have been described:
  • 25
  • 52
    • 58949102186 scopus 로고    scopus 로고
    • note
    • The low yield observed in the formation of 26 is mainly due to the instability of the compound, which rapidly decomposes at rt.
  • 53
    • 58949084737 scopus 로고    scopus 로고
    • For recent accounts dealing with gold-catalyzed Meyer-Schuster rearrangement, see:
    • For recent accounts dealing with gold-catalyzed Meyer-Schuster rearrangement, see:
  • 60
    • 58949088609 scopus 로고    scopus 로고
    • For related Au-catalyzed substitutions on benzylic positions, see: (a) Ref. 13;
    • For related Au-catalyzed substitutions on benzylic positions, see: (a) Ref. 13;
  • 62
    • 34247172519 scopus 로고    scopus 로고
    • These reactions have recently been described:
    • These reactions have recently been described:. Guo S., Song F., and Liu Y. Synlett (2007) 964-968
    • (2007) Synlett , pp. 964-968
    • Guo, S.1    Song, F.2    Liu, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.