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An Efficient and Recyclable Ionic Liquid-Supported Proline Catalyzed Knoevenagel Condensation
Joint Authors
Zhuo, Chen
Hui, Xie
Xian, Dong
Jian-wei, Wu
Source
Issue
Vol. 2011, Issue 2011 (31 Dec. 2011), pp.1-5, 5 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2011-04-10
Country of Publication
Egypt
No. of Pages
5
Main Subjects
Abstract EN
The Knoevenagel condensation reaction of aldehydes with malononitrile was described in this study, which was catalyzed by an efficient and recyclable ionic liquid-supported proline.
The method represented an attractive alternative to the classical synthesis strategies and exhibited the advantage of performing homogeneous chemistry on a large scale additionally avoided large excesses of reagents.
The products were obtained in good yields and reasonable purities without the need for further chromatographic purification.
Moreover, the catalyst could be reused for at least four times.
American Psychological Association (APA)
Zhuo, Chen& Xian, Dong& Jian-wei, Wu& Hui, Xie. 2011. An Efficient and Recyclable Ionic Liquid-Supported Proline Catalyzed Knoevenagel Condensation. ISRN Organic Chemistry،Vol. 2011, no. 2011, pp.1-5.
https://search.emarefa.net/detail/BIM-489700
Modern Language Association (MLA)
Zhuo, Chen…[et al.]. An Efficient and Recyclable Ionic Liquid-Supported Proline Catalyzed Knoevenagel Condensation. ISRN Organic Chemistry No. 2011 (2011), pp.1-5.
https://search.emarefa.net/detail/BIM-489700
American Medical Association (AMA)
Zhuo, Chen& Xian, Dong& Jian-wei, Wu& Hui, Xie. An Efficient and Recyclable Ionic Liquid-Supported Proline Catalyzed Knoevenagel Condensation. ISRN Organic Chemistry. 2011. Vol. 2011, no. 2011, pp.1-5.
https://search.emarefa.net/detail/BIM-489700
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-489700