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Volumn 47, Issue 11, 2006, Pages 1699-1703

The Knoevenagel reaction: Analysis and recycling of the ionic liquid medium

Author keywords

Alternative technologies; Clean technology; Condensation reaction; Ionic liquid technologies; Knoevenagel reaction; Organic synthesis; Pollution prevention; Reuse; Scope of substrate

Indexed keywords

ALDEHYDE; IONIC LIQUID; KETONE DERIVATIVE;

EID: 32244443296     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.01.059     Document Type: Article
Times cited : (62)

References (37)
  • 9
    • 32244444209 scopus 로고    scopus 로고
    • For a thematic issue focusing on the application of IL technology in synthetic processes, see: issue 1 of J. Mol. Catal. A: Chem. 2004, 214.
    • (2004) J. Mol. Catal. A: Chem. , Issue.1 , pp. 214
  • 11
    • 27144456437 scopus 로고    scopus 로고
    • Ionic Liquids IIIA: Fundamentals, Progress, Challenges, and Opportunities-Properties and Structure
    • American Chemical Society Washington, DC
    • Ionic Liquids IIIA: Fundamentals, Progress, Challenges, and Opportunities-Properties and Structure R.D. Rogers K.R. Seddon ACS Symposium Series No. 901 2005 American Chemical Society Washington, DC
    • (2005) ACS Symposium Series No. 901
    • Rogers, R.D.1    Seddon, K.R.2
  • 12
    • 27144456437 scopus 로고    scopus 로고
    • Ionic Liquids IIIA: Fundamentals, Progress, Challenges, and Opportunities-Transformations and Processes
    • American Chemical Society Washington, DC
    • Ionic Liquids IIIA: Fundamentals, Progress, Challenges, and Opportunities-Transformations and Processes R.D. Rogers K.R. Seddon ACS Symposium Series No. 902 2005 American Chemical Society Washington, DC
    • (2005) ACS Symposium Series No. 902
    • Rogers, R.D.1    Seddon, K.R.2
  • 16
    • 85066115200 scopus 로고
    • For an extensive review on the application of malononitrile in the Knoevenagel reaction, see: A.J. Fatiadi Synthesis 1978 165
    • (1978) Synthesis , pp. 165
    • Fatiadi, A.J.1
  • 20
    • 0000248247 scopus 로고
    • For general reviews on the Knoevenagel reaction, see: G. Jones Org. React. 15 1967 204
    • (1967) Org. React. , vol.15 , pp. 204
    • Jones, G.1
  • 29
    • 32244437757 scopus 로고    scopus 로고
    • note
    • 2, 3 mL fractions] to afford the title compound. Spectral data obtained on each system were in agreement with previous reports.
  • 31
    • 32244440460 scopus 로고    scopus 로고
    • note
    • 6] and trace amounts of unreacted malononitrile. The spectral data of the recycling experiments were in agreement with the data obtained during the scope of substrate survey.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.