Triethylamine: a potential N-base surrogate for pyridine in Knoevenagel condensation of aromatic aldehydes and malonic acid
Author:
Affiliation:
1. DBT-ICT Centre for Energy Biosciences
2. Institute of Chemical Technology
3. Mumbai
4. India
5. Department of Chemical Engineering
Abstract
Triethyl amine was successfully examined as a potent N-base surrogate for Knoevenagel condensation to produce cinnamic acids without compromising product yield.
Funder
Department of Biotechnology , Ministry of Science and Technology
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,General Chemistry,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2016/NJ/C5NJ03125G
Reference37 articles.
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2. Novel caffeic acid derivatives: extremely potent inhibitors of 12-lipoxygenase
3. Convenient Formation of 4-Hydroxyalk-2-en-1-one Functionality via A Knoevenagel-type Carbon Chain Elongation Reaction of Aldehyde with 1-Arylsulfinylalkan-2-one
4. Colored and Luminous Aliphatic Polyester via One-Pot Intra- and Intermolecular Knoevenagel Reactions
5. Aqueous Extract of Acacia concinna Pods: An Efficient Surfactant Type Catalyst for Synthesis of 3-Carboxycoumarins and Cinnamic Acids via Knoevenagel Condensation
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