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Volumn 50, Issue 27, 2009, Pages 3942-3944

Palladium-catalysed direct alkenylation of sydnones

Author keywords

[No Author keywords available]

Indexed keywords

BROMINE DERIVATIVE; PALLADIUM; SYDNONE DERIVATIVE;

EID: 65549108740     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.04.075     Document Type: Article
Times cited : (41)

References (67)
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    • (2006) Chem. Commun. , pp. 1253
    • Campeau, L.-C.1    Fagnou, K.2
  • 45
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    • For reviews on sydnones, see:
    • For reviews on sydnones, see:. Stewart F.H.C. Chem. Rev. 64 (1964) 129
    • (1964) Chem. Rev. , vol.64 , pp. 129
    • Stewart, F.H.C.1
  • 47
    • 0016140621 scopus 로고
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    • (1974) J. Med. Chem. , vol.17 , pp. 1337
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    • 0034112044 scopus 로고    scopus 로고
    • For the transformation of sydnones into oxadiazolinones with bromine in acetic anhydride, see:
    • For the transformation of sydnones into oxadiazolinones with bromine in acetic anhydride, see:. Mallur S.G., and Badami B.V. Il Farmaco 55 (2000) 65
    • (2000) Il Farmaco , vol.55 , pp. 65
    • Mallur, S.G.1    Badami, B.V.2
  • 64
    • 59849085075 scopus 로고    scopus 로고
    • For the palladium-catalysed direct alkenylation, benzylation and alkylation of ethyl oxazole-4-carboxylate, see:
    • For the palladium-catalysed direct alkenylation, benzylation and alkylation of ethyl oxazole-4-carboxylate, see:. Verrier C., Hoarau C., and Marsais F. Org. Biomol. Chem. 7 (2009) 647
    • (2009) Org. Biomol. Chem. , vol.7 , pp. 647
    • Verrier, C.1    Hoarau, C.2    Marsais, F.3
  • 65
    • 47749125841 scopus 로고    scopus 로고
    • For the palladium-catalysed direct alkenylation of pyridine N-oxides with acrylates, see:
    • For the palladium-catalysed direct alkenylation of pyridine N-oxides with acrylates, see:. Cho S.H., Hwang S.J., and Chang S. J. Am. Chem. Soc. 130 (2008) 9254
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 9254
    • Cho, S.H.1    Hwang, S.J.2    Chang, S.3
  • 66
    • 65549159413 scopus 로고    scopus 로고
    • note
    • 4 and filtered. The volatiles were removed in vacuo and the mixture was purified by flash chromatography (5:1 PE/EtOAc on silica gel) to give 3-phenyl-4-(1-phenylvinyl)sydnone (64 mg, 78%).
  • 67
    • 0037677148 scopus 로고    scopus 로고
    • For the Sonogashira cross-coupling reactions of sydnones, see:
    • For the Sonogashira cross-coupling reactions of sydnones, see:. Turnbull K., Krein D.M., and Tullis S.A. Synth. Commun. 33 (2003) 2209
    • (2003) Synth. Commun. , vol.33 , pp. 2209
    • Turnbull, K.1    Krein, D.M.2    Tullis, S.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.