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Volumn 42, Issue 6, 2013, Pages 583-585

Synthesis of diverse aromatic oxophosphorus compounds by the Michaelis-Arbuzov-type reaction of arynes

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EID: 84878692146     PISSN: 03667022     EISSN: 13480715     Source Type: Journal    
DOI: 10.1246/cl.130116     Document Type: Article
Times cited : (62)

References (30)
  • 2
    • 0034680581 scopus 로고    scopus 로고
    • Selected examples for bioacitive organophosphorus compounds, see: a) K. T. Sprott, P. R. Hanson, J. Org. Chem. 2000, 65, 7913.
    • (2000) J. Org. Chem. , vol.65 , pp. 7913
    • Sprott, K.T.1    Hanson, P.R.2
  • 6
    • 84878738498 scopus 로고    scopus 로고
    • ed. by P. J. Murphy, Oxford University Press, Oxford, Chap. 2
    • Both nucleophilic substitution approaches using electrophilic and nucleophilic organophosphorus reagents are known. See: M. L. Clarke, J. M. J. Williams, in Organophosphorus Reagents, ed. by P. J. Murphy, Oxford University Press, Oxford, 2004, Chap. 2.
    • (2004) Organophosphorus Reagents
    • Clarke, M.L.1    Williams, J.M.J.2
  • 9
    • 84983960649 scopus 로고
    • c) P. Tavs, Chem. Ber. 1970, 103, 2428.
    • (1970) Chem. Ber. , vol.103 , pp. 2428
    • Tavs, P.1
  • 23
    • 48249089353 scopus 로고    scopus 로고
    • and references therein
    • R. Sanz, Org. Prep. Proced. Int. 2008, 40, 215, and references therein.
    • (2008) Org. Prep. Proced. Int. , vol.40 , pp. 215
    • Sanz, R.1
  • 28
    • 0003975691 scopus 로고
    • Academic Press, New York
    • Examples for trapping anionic intermediates generated from arynes and nucleophiles by carbon dioxide, see: a) R. W. Hoffmann, Dehydrobenzene and Cycloalkynes, Academic Press, New York, 1967, p. 170.
    • (1967) Dehydrobenzene and Cycloalkynes , pp. 170
    • Hoffmann, R.W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.