期刊
JOURNAL OF CHEMICAL RESEARCH
卷 -, 期 1, 页码 22-24出版社
SCIENCE REVIEWS 2000 LTD
DOI: 10.3184/030823409X12615671424822
关键词
Knoevenagel condensation; L-arginine; ionic liquid
L-Arginine catalysed the Knoevenagel condensations of aromatic, heteroaromatic and alpha,beta-unsaturated aldehydes with malononitrile and acetylacetone to afford alpha,beta-unsaturated nitriles and ketones. The reactions were carried out at room temperature in the ionic liquid, 1-ethyl-3-methylimidazolium ethylsulfate. Moderate to excellent yields (45-100%) were achieved. The L-arginine/ionic liquid combination was successfully recycled for five runs without significant loss of activity.
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