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Volumn 64, Issue 26, 2008, Pages 5982-5986

Palladium-catalyzed direct oxidative vinylation of thiophenes and furans under weakly basic conditions

Author keywords

C H bond cleavage; Heteroarenes; Oxidative vinylation; Palladium catalyst

Indexed keywords

ALKENE; CARBON; COPPER; DRUG ADDITIVE; FURAN DERIVATIVE; LITHIUM SALT; OXIDIZING AGENT; PALLADIUM; THIOPHENE DERIVATIVE;

EID: 43849104916     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.01.058     Document Type: Article
Times cited : (44)

References (58)
  • 14
    • 43849106241 scopus 로고    scopus 로고
    • Reviews:
    • Reviews:
  • 31
    • 43849107981 scopus 로고    scopus 로고
    • Reviews:
    • Reviews:
  • 37
    • 1242352467 scopus 로고    scopus 로고
    • For a stoichiometric version, see:
    • Tani M., Sakaguchi S., and Ishii Y. J. Org. Chem. 69 (2004) 1221 For a stoichiometric version, see:
    • (2004) J. Org. Chem. , vol.69 , pp. 1221
    • Tani, M.1    Sakaguchi, S.2    Ishii, Y.3
  • 39
    • 43849089900 scopus 로고    scopus 로고
    • For intermolecular direct vinylation reactions of indoles and pyrroles, see:
    • For intermolecular direct vinylation reactions of indoles and pyrroles, see:
  • 53
    • 43849090989 scopus 로고    scopus 로고
    • A few examples for the vinylation of a relatively more acid tolerable substrate, 1,2-methylenedioxybenzene in propionic acid at 70-90 °C has been reported. In this case, an excess amount of the aromatic substrate (3-7 equiv) is usually employed.
    • A few examples for the vinylation of a relatively more acid tolerable substrate, 1,2-methylenedioxybenzene in propionic acid at 70-90 °C has been reported. In this case, an excess amount of the aromatic substrate (3-7 equiv) is usually employed.
  • 54
    • 43849096300 scopus 로고    scopus 로고
    • Ref. 7d;
    • Ref. 7d;


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.