2011
DOI: 10.1016/j.ultsonch.2010.04.009
|View full text |Cite
|
Sign up to set email alerts
|

Ultrasound-assisted one-pot, four component synthesis of 4-aryl 3,4-dihydropyridone derivatives

Abstract: The condensation of Meldrum's acid, aromatic aldehydes, alkyl acetoacetates and ammonium acetate in glacial acetic acid under ultrasound irradiation at room temperature results in the formation of 3,4-dihydropyridone derivatives (4a-p) in 85-96% yields. Compared with conventional methods, the main advantages of the present procedure are milder conditions, shorter reaction times and higher yields.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
8
0

Year Published

2011
2011
2019
2019

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 36 publications
(8 citation statements)
references
References 51 publications
0
8
0
Order By: Relevance
“…Therefore, recently, ultrasonic irradiation technique has received considerable attention of researchers. [21][22][23][24][25] In continuation of our ongoing research on the Michael addition of imides and amides to unsaturated systems, 26,27 we report here an efficient strategy for synthesis of a series of DPH derivatives by Michael addition of this compound to α,β-unsaturated esters under ultrasound irradiation (Scheme 2).…”
Section: Scheme 1 Nucleophilic Reactions Of Diverse Positions Of Dphmentioning
confidence: 99%
“…Therefore, recently, ultrasonic irradiation technique has received considerable attention of researchers. [21][22][23][24][25] In continuation of our ongoing research on the Michael addition of imides and amides to unsaturated systems, 26,27 we report here an efficient strategy for synthesis of a series of DPH derivatives by Michael addition of this compound to α,β-unsaturated esters under ultrasound irradiation (Scheme 2).…”
Section: Scheme 1 Nucleophilic Reactions Of Diverse Positions Of Dphmentioning
confidence: 99%
“…In addition, the reactions carried out in synthesis of organic compounds should be fast and facile, and the obtained products should be easily separated and purified after the synthesis. So, the implementation of new procedures and strategies is required for these reasons …”
Section: Introductionmentioning
confidence: 99%
“…Furthermore, MCRs are easy to perform, inexpensive, quick, energy efficient and experimental procedures are relatively simple (1). Recently, the application of ultrasonic irradiation in chemical syntheses has received much attention (2)(3)(4)(5). On the other hand, designing MCRs under ultrasonic irradiation is another attractive area in synthetic organic chemistry.…”
Section: Introductionmentioning
confidence: 99%