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Volumn 126, Issue 17, 2004, Pages 5350-5351

Phosphine Catalyzed α-Arylation of Enones and Enals Using Hypervalent Bismuth Reagents: Regiospecific Enolate Arylation via Nucleophilic Catalysis

Author keywords

[No Author keywords available]

Indexed keywords

BISMUTH; PHOSPHINE; REAGENT;

EID: 2342449218     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja048987i     Document Type: Article
Times cited : (88)

References (40)
  • 15
    • 0030664209 scopus 로고    scopus 로고
    • For metal-catalyzed arylation of unmodified carbonyl compounds, see: (a) Palucki, M.; Buchwald, S. L. J. Am. Chem. Soc. 1997, 119, 11108.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 11108
    • Palucki, M.1    Buchwald, S.L.2
  • 24
    • 0034249671 scopus 로고    scopus 로고
    • In the Heck arylation of α,β-unsaturated carbonyl compounds, products of α-arylation are observed as side products: Beletskaya, I. P.; Cheprakov, A. V. Chem. Rev. 2000, 100, 3009.
    • (2000) Chem. Rev. , vol.100 , pp. 3009
    • Beletskaya, I.P.1    Cheprakov, A.V.2
  • 25
    • 0010912252 scopus 로고
    • Decomposition of aryl diazonium salts in the presence of cinnamic acid esters afford products of α-arylation in poor yield: Koelsch, C. F.; Boekelheide, V. J. Am. Chem. Soc. 1944, 66, 412.
    • (1944) J. Am. Chem. Soc. , vol.66 , pp. 412
    • Koelsch, C.F.1    Boekelheide, V.2
  • 26


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.