Recent Advances in the Synthesis of Coumarin Derivatives via Knoevenagel Condensation: A Review

2014 ◽  
Vol 44 (19) ◽  
pp. 2756-2788 ◽  
Author(s):  
Rajesh H. Vekariya ◽  
Hitesh D. Patel
2016 ◽  
Vol 20 (7) ◽  
pp. 798-828 ◽  
Author(s):  
Abhay S. Zambare ◽  
Firoz A. Kalam Khan ◽  
Sureshchandra P. Zambare ◽  
Shantanu D. Shinde ◽  
Jaiprakash N. Sangshetti

2022 ◽  
Author(s):  
Qiao Li ◽  
Yang Zhao ◽  
Zhigang Niu ◽  
Enju Wang

Abstract Two coumarin derivatives, 7-diethylamino-3-(4-nitrophenyl)coumarin (DNC) and 7-hydroxy-3-(4-nitrophenyl)coumarin (HNC), were synthesized via Knoevenagel condensation of salicylaldehyde derivatives with 4-nitrophenylacetonitrile and then cyclization reaction. Both of them were characterized by single-crystal X-ray diffraction. The molecules of DNC are stacked via π-π interaction, while the hydrogen bond interactions instead of π-π interaction were observed in the crystal packing of HNC. Both of DNC and HNC showed solvatochromic properties and aggregation-induced emission (AIE) activities, but the AIE characteristics of them were entirely different. HNC exhibited an AIE phenomenon as the result of the restriction of twisted intramolecular charge transfer (TICT), while DNC emited peculiar dual fluorescence which was assigned to the emission based on the inhibition of TICT state formation and the emission from the TICT state respectively.


2021 ◽  
Vol 7 (1) ◽  
pp. 62-68
Author(s):  
Juliana Jumal ◽  
Norhanis Sakinah

Coumarin and its derivatives represent one of the most active curriculums of compound possessing a broad spectrum of biological activity along with other applications such as insecticide and fragrance. There are various methodologies developed for the synthesis of coumarins. Classical routes to coumarins include Pechmann condensation, Knoevenagel condensation, Perkin reaction, and Wittig condensation reactions. Researchers have carried out adjustments and improvements to increase the efficacy and overcome the limitations from the classical route. In this review outline, coumarin derivatives were characterized by using FTIR and Hydrogen NMR spectroscopy. This review paper focuses on various synthesis and characterization techniques to analyze coumarin derivatives and their potential application in various fields.


ChemInform ◽  
2016 ◽  
Vol 47 (19) ◽  
Author(s):  
Abhay S. Zambare ◽  
Firoz A. Kalam Khan ◽  
Sureshchandra P. Zambare ◽  
Shantanu D. Shinde ◽  
Jaiprakash N. Sangshetti

2019 ◽  
Vol 4 (31) ◽  
pp. 9211-9215 ◽  
Author(s):  
Leila Dinparast ◽  
Salar Hemmati ◽  
Gokhan Zengin ◽  
Ali Akbar Alizadeh ◽  
Mir Babak Bahadori ◽  
...  

2021 ◽  
Vol 09 ◽  
Author(s):  
Krishnappa B Badiger ◽  
Santosh Y Khatavi ◽  
Prashant B Hiremath ◽  
Kantharaju Kamanna

Background: The present work describes an eco-friendly and sustainable approach for the Knoevenagel condensation of an aromatic aldehyde with ethyl cyanoacetate, and salicylaldehyde with Meldrum acid for the synthesis of ethyl benzylidenecyanoacetate and 3-carboxy coumarin (2-oxo-2H-1-benzopyran) derivatives, respectively. The reaction performed under greener catalytic media Water Extract of Watermelon Fruit Peel Ash (WEWFPA) is an eco-friendly protocol derived from the agro-waste feedstock. Various protocols have been reported for the synthesis of Knoevenagel condensation reaction using a hazardous catalyst or/and solvent found toxic to the environment, reaction time longer, poor yield, and required purification of the final product. The present method provides several added advantages of being completely greener, economic, giving high yield, inexpensive catalyst, and the final product isolated in pure form with good yield. Objective: The objective of the study was to develop a green methodology for the synthesis of ethyl benzylidenecyanoacetate and 3-carboxy coumarin derivatives. Results: The agro-waste based catalyst developed avoids the use of external inorganic/organic base, additives, and solvent-free synthesis of Knoevenagel condensation of ethyl benzylidenecyanoacetate and 3-carboxy coumarin derivatives under rt and microwave irradiation, respectively described. The microwave irradiation condition requires less time for the completion of the reaction and also gave better yield isolation Methods: We have demonstrated WEWFPA as a greener homogenous agro-waste is employed under rt stirring and microwave irradiation for the economic synthesis of ethyl benzylidenecyanoacetate and 3-carboxy coumarin derivatives. The developed method was found robust, non-hazardous and solvent-free with simple work-up gave target product. Conclusion: In conclusion, we have established an efficient, simple, agro-waste based catalytic approach for the synthesis of ethylbenzylidenecyanoacetate and 3-carboxy coumarin derivatives employing WEWFPA as an efficient catalyst under rt stirring and microwave synthesis, respectively. The method is a greener, economical and eco-friendly approach for the synthesis of Knoevenagel condensation products. The advantages of the present approach are solvent-free, no external metal, chemical base free, short reaction time and isolated product in good to excellent yields. The catalyst is agro-waste derived, which has abundant in natural sources, thus making the present approach a greener one.


2020 ◽  
Vol 17 (7) ◽  
pp. 828-842
Author(s):  
Nader Ghaffari Khaligh ◽  
Mohd Rafie Johan

α,β-Unsaturated acids are well-known and useful reagents, and they have been applied in different fields due to their fascinating properties. The catalytic Knoevenagel condensation reaction is one of the most remarkable methods for the formation of C=C bonds. The multi-substituted alkenes can be obtained from the reaction of carbonyl and active methylene compounds in the presence of base catalysts, Brönsted catalysts, Lewis acid catalysts, or ionic liquids. In terms of providing both desirable structural diversity and compound libraries, Doebner-Knoevenagel condensation is the most efficient strategy. There is a high demand for an efficient, rapid, environment-friendly, and sustainable catalytic protocol under milder conditions for the stereoselective synthesis of Knoevenagel products, which can tolerate a wide variety of functions. Carrying out the transformations through alternative reagents, catalysts, or methods provides a valuable and broad space for selectivity. Herein, the recent advances in the synthesis of structurally diversified Knoevenagel products using nanocatalysts are reviewed.


Tetrahedron ◽  
2014 ◽  
Vol 70 (3) ◽  
pp. 551-572 ◽  
Author(s):  
Leonid G. Voskressensky ◽  
Alexey A. Festa ◽  
Alexey V. Varlamov

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