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Volumn 351, Issue 18, 2009, Pages 3207-3216

Preparation of arylphosphonates by palladium(O)-catalyzed cross-coupling in the presence of acetate additives: Synthetic and mechanistic studies

Author keywords

Acetate additives; Arylphosphonates; H phosphonate diesters; Nucleotide analogues; Palladium catalyzed cross coupling

Indexed keywords


EID: 73349129342     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200900590     Document Type: Article
Times cited : (151)

References (70)
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    • Since there was a remote possibility that lack of the reaction between bromobenzene and diethyl H-phosphonate in the presence of high acetate concentration (Table 2, entries 3 and 5) could be due to consumption of bromobenzene in the reaction with acetate ions see, for example, T. Forngren, Y. Andersson, B. Lamm, B. Langström, Acta Chem. Scand. 1998, 52, 475-479, we checked the reaction mixtures for a possible presence of phenyl acetate. Since neither 1H NMR spectroscopy nor TLC analysis revealed the presence of this compound, such a possibility seemed to be less likely
    • 1H NMR spectroscopy nor TLC analysis revealed the presence of this compound, such a possibility seemed to be less likely.
  • 69
    • 33745132807 scopus 로고    scopus 로고
    • Nucleic Acid Drugs
    • Eds, T. Dingermann, D. Steinhilber, G. Folkers, Wiley-VCH, Weinheim
    • J. W. Engels, J. Parsch, Nucleic Acid Drugs, in: Molecular Biology in Medicinal Chemistry, (Eds.: T. Dingermann, D. Steinhilber, G. Folkers), Wiley-VCH, Weinheim, 2005.
    • (2005) Molecular Biology in Medicinal Chemistry
    • Engels, J.W.1    Parsch, J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.