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Volumn 694, Issue 22, 2009, Pages 3674-3678

Catalyst-free alkanoylation of aromatic rings via arylstannanes. Scope and limitations

Author keywords

Aromatic electrophilic acylation; Arylstannanes; Tertiary alkyl ketones

Indexed keywords

AROMATIC ELECTROPHILIC ACYLATION; AROMATIC RINGS; ARYL KETONES; ARYLSTANNANES; CATALYST-FREE; DICHLOROBENZENES; ISOLATED YIELD; REGIOSELECTIVE SYNTHESIS; TERTIARY ALKYL KETONES;

EID: 69949086751     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jorganchem.2009.07.019     Document Type: Short Survey
Times cited : (12)

References (23)
  • 5
    • 69949105144 scopus 로고    scopus 로고
    • Ref, 1, page 1532
    • Ref. [1], page 1532.
  • 12
    • 0004063249 scopus 로고    scopus 로고
    • The remaining trimethylstannyl group could be substituted by different electrophiles., VCH, Weinheim
    • The remaining trimethylstannyl group could be substituted by different electrophiles. Davies A.G. Organotin Chemistry (1997), VCH, Weinheim
    • (1997) Organotin Chemistry
    • Davies, A.G.1
  • 22
    • 42149092690 scopus 로고    scopus 로고
    • Authors thank Dr. Greaney for the personal information about preparation of silicagel doped with KF
    • Ferrer Flegeau E., Popkin M.E., and Greaney M.F. J. Org. Chem. 73 (2008) 3303 Authors thank Dr. Greaney for the personal information about preparation of silicagel doped with KF
    • (2008) J. Org. Chem. , vol.73 , pp. 3303
    • Ferrer Flegeau, E.1    Popkin, M.E.2    Greaney, M.F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.