메뉴 건너뛰기




Volumn 77, Issue 20, 2012, Pages 9426-9428

A 2,6-diformylnaphthalene-1,8:4,5-bis(dicarboximide): Synthesis and knoevenagel condensation with malononitrile

Author keywords

[No Author keywords available]

Indexed keywords

ELECTROCHEMICAL DATA; KNOEVENAGEL CONDENSATION; MALONONITRILES; NAPHTHALENE DIIMIDE; OZONOLYSIS; UV-VIS ABSORPTIONS;

EID: 84867718015     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo301876v     Document Type: Article
Times cited : (21)

References (26)
  • 4
  • 19
    • 84867694335 scopus 로고    scopus 로고
    • The Vilsmeier-Haack reaction
    • Springer: Berlin, Heidelberg
    • Li, J. J. The Vilsmeier-Haack reaction. Name Reactions; Springer: Berlin, Heidelberg, 2009; pp 558-559.
    • (2009) Name Reactions , pp. 558-559
    • Li, J.J.1
  • 25
    • 0022766861 scopus 로고
    • Multiple reduction features are observed, perhaps in part due to polymerization of the vinyl species initiated by the radical anion. This behavior is consistent with what is seen for other redox-active styrene-like species (;). The value given is the peak potential observed in a differential pulse voltammogram.
    • Multiple reduction features are observed, perhaps in part due to polymerization of the vinyl species initiated by the radical anion. This behavior is consistent with what is seen for other redox-active styrene-like species (Ortega, J. M.; Menolasina, S.; De Marquez, O. P.; Marquez., J. Polymer 1986, 27, 1304-1306). The value given is the peak potential observed in a differential pulse voltammogram.
    • (1986) Polymer , vol.27 , pp. 1304-1306
    • Ortega, J.M.1    Menolasina, S.2    De Marquez, O.P.3    Marquez, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.