An Efficient and Recyclable Ionic Liquid-Supported Proline Catalyzed Knoevenagel Condensation

Joint Authors

Zhuo, Chen
Hui, Xie
Xian, Dong
Jian-wei, Wu

Source

ISRN Organic Chemistry

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

Chemistry

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