Coumarin compounds have great interest for their wide range of medicinal and pharmacological properties as well as for their fluorescent properties. Simple coumarins are being the major precursor for the synthesis of most of the coumarin derivatives. Simple coumarin (C1) was synthesized by using Perkin condensation reaction whereas 7-hydroxy coumarin (C2) and 7-hydroxy-4-methyl coumarin (C3) were synthesized by using Pechmann condensation reaction. Solvent combination which gives higher recovery percentage on recrystallization was found out. The synthesized simple coumarins were characterized by using spectroscopic analysis (UV, IR, 1H and 13C NMR). The solvent combination which gave higher recovery percentage for C1 and C3 were 40 % aqueou...
Abstract. Reactions of 4-chloro-2-oxo-2H-chromene-3-carbonitrile (1) with 4-methylpyridin-2-ylamine ...
The synthesis of five naturally occurring polyoxygenated coumarins is described. It concerns two 5,6...
Synthesis of Coumarins from Phenols and β-Ketonic Esters. Part III. Use of Various Condensing Agents
Knoevenagel condensation reaction (KCR) and Pechmann condensation reaction are the simplest and most...
Coumarins are a family of naturally occurring compounds. Coumarin motifs are present in numerous nat...
For several decades, coumarins have attracted considerable attention due to the fact of their applic...
In this article we describe a new methodology for the total synthesis of 3,4-unsubstituted coumarin...
The current study was designed to investigate the reactivity of 3-acetyl-6-bromocoumarintowards a va...
Many organic and medicinal chemists are interested in the coumarin compounds because of their potent...
A simple preparation of a coumarin product via an Pechmann condensation catalyzed by sulfuric acid. ...
Two coumarin derivatives: 5,7-di Hydroxy-4-Methyl Coumarin (1) and 6-hydroxy-1-methyl-3H-benzo[f]chr...
During the last few decades the interest in the synthesis and investigation of different coumarin de...
Coumarin derivatives have a myriad of applications in medical science, biomedical research, and many...
Coumarin (1,2-Benzopyrone or 2H-1-benzopyran-2-one, or phenylpropanoids, 1) and its derivatives (cou...
Coumarin derivatives are used as fluorescent dyes and medicines. They also have some notable physiol...
Abstract. Reactions of 4-chloro-2-oxo-2H-chromene-3-carbonitrile (1) with 4-methylpyridin-2-ylamine ...
The synthesis of five naturally occurring polyoxygenated coumarins is described. It concerns two 5,6...
Synthesis of Coumarins from Phenols and β-Ketonic Esters. Part III. Use of Various Condensing Agents
Knoevenagel condensation reaction (KCR) and Pechmann condensation reaction are the simplest and most...
Coumarins are a family of naturally occurring compounds. Coumarin motifs are present in numerous nat...
For several decades, coumarins have attracted considerable attention due to the fact of their applic...
In this article we describe a new methodology for the total synthesis of 3,4-unsubstituted coumarin...
The current study was designed to investigate the reactivity of 3-acetyl-6-bromocoumarintowards a va...
Many organic and medicinal chemists are interested in the coumarin compounds because of their potent...
A simple preparation of a coumarin product via an Pechmann condensation catalyzed by sulfuric acid. ...
Two coumarin derivatives: 5,7-di Hydroxy-4-Methyl Coumarin (1) and 6-hydroxy-1-methyl-3H-benzo[f]chr...
During the last few decades the interest in the synthesis and investigation of different coumarin de...
Coumarin derivatives have a myriad of applications in medical science, biomedical research, and many...
Coumarin (1,2-Benzopyrone or 2H-1-benzopyran-2-one, or phenylpropanoids, 1) and its derivatives (cou...
Coumarin derivatives are used as fluorescent dyes and medicines. They also have some notable physiol...
Abstract. Reactions of 4-chloro-2-oxo-2H-chromene-3-carbonitrile (1) with 4-methylpyridin-2-ylamine ...
The synthesis of five naturally occurring polyoxygenated coumarins is described. It concerns two 5,6...
Synthesis of Coumarins from Phenols and β-Ketonic Esters. Part III. Use of Various Condensing Agents