Author(s):
Albuquerque, Hélio 
; Santos, Clementina M.M. ; Silva, Artur ; Cavaleiro, José A.S.
Date: 2013
Persistent ID: http://hdl.handle.net/10198/9360
Origin: Biblioteca Digital do IPB
Document details
Synthesis of (E)-2-(4-Arylbut-1-en-3-ynyl)-4H-chromen-4-ones
Description
Chromones are a well-known class of naturally occurring oxygencontaining heterocyclic compounds; many of them playing important biological functions in nature [1]. Although 2-methylchromones are one of the scarcest classes of natural chromones, their synthesis and reactivity is well studied. They can participate in several chemical transformations such as oxidation, thiation, hydrogenation, photolysis, cycloaddition and condensation reactions, being useful targets in the synthesis of novel heterocyclic compounds [2]. The acidity of the 2- methyl group, due to the low electron density at C-2 caused by oxygen atom and the α,β-unsaturated ketone system, led us to explore the condensation of 2-methylchromones [3] with propargyl aldehydes [4].
Chromones are a well-known class of naturally occurring oxygencontaining heterocyclic compounds; many of them playing important biological functions in nature [1]. Although 2-methylchromones are one of the scarcest classes of natural chromones, their synthesis and reactivity is well studied. They can participate in several chemical transformations such as oxidation, thiation, hydrogenation, photolysis, cycloaddition and condensation reactions, being useful targets in the synthesis of novel heterocyclic compounds [2]. The acidity of the 2- methyl group, due to the low electron density at C-2 caused by oxygen atom and the α,β-unsaturated ketone system, led us to explore the condensation of 2-methylchromones [3] with propargyl aldehydes [4].
Document Type
Conference Object
Language English
Language English
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