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Volumn , Issue 23, 2007, Pages 2405-2407

Insertion of arynes into carbon-halogen σ-bonds: Regioselective acylation of aromatic rings

Author keywords

[No Author keywords available]

Indexed keywords

ACID HALIDE; AROMATIC COMPOUND; CARBON; HALOGEN; POLYCYCLIC AROMATIC HYDROCARBON;

EID: 34249988854     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b701581j     Document Type: Article
Times cited : (56)

References (22)
  • 20
    • 84942819527 scopus 로고    scopus 로고
    • This result confirms that the present reaction indeed proceeds through an aryne intermediate
    • This result confirms that the present reaction indeed proceeds through an aryne intermediate
  • 21
    • 84942832664 scopus 로고    scopus 로고
    • Owing to an electron-withdrawing inductive effect and a steric effect of the methoxy moiety, 3-methoxybenzyne generally accepts a nucleophilic attack at the meta position to the methoxy moiety A review on electrophilic coupling of arynes:
    • Owing to an electron-withdrawing inductive effect and a steric effect of the methoxy moiety, 3-methoxybenzyne generally accepts a nucleophilic attack at the meta position to the methoxy moiety
  • 22
    • 33750456293 scopus 로고
    • B. M. Trost and I. Fleming, Pergamon Press, Oxford, pp. 483-515
    • S. V. Kessar, in Comprehensive Organic Synthesis, ed., B. M. Trost, and, I. Fleming,, Pergamon Press, Oxford, 1991, vol. 4, pp. 483-515
    • (1991) Comprehensive Organic Synthesis, Ed.
    • Kessar In, S.V.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.