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Synthesis,structure and cytotoxicity of new 2‐[(3‐aminopropyl)dimethylsilyl]‐5‐furfural diethylacetals and 2‐[(3‐aminopropyl)dimethylsilyl]‐5‐phenylfurans
Authors:Luba Ignatovich  Velta Muravenko  Jana Spura  Jury Popelis  Ilona Domrachova  Irina Shestakova
Institution:Latvian Institute of Organic Synthesis, , Riga, LV 1006 Latvia
Abstract:Novel 2‐(3‐aminopropyl)dimethylsilyl]‐5‐furfural diethylacetals and 2‐(3‐aminopropyl)di‐methylsilyl]‐5‐phenylfurans have been synthesized by a hydrosilylation reaction of aliphatic and heterocyclic N‐allylamines in the presence of the Speier's catalyst. The effects of the structure of the amine and nature of organic substituent at the furan ring on the cytotoxicity of the new compounds have been studied. Copyright © 2013 John Wiley & Sons, Ltd.
Keywords:2‐[(3‐aminopropyl)dimethylsilyl]‐5‐furfural diethylacetals  2‐[(3‐aminopropyl)‐dimethylsilyl]‐5‐phenylfurans  hydrosilylation  1H  13C  29Si NMR  cytotoxic activity
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