2015
DOI: 10.3906/kim-1404-54
|View full text |Cite
|
Sign up to set email alerts
|

Green and efficient synthesis of novel bispyrazoles through a tandem Knoevenagel and Michael type reaction using nanowire zinc oxide as a powerful and recyclable catalyst

Abstract: Zinc oxide nanowires (ZnO NWs) were prepared and characterized by scanning electron microscopy, powder X-ray diffraction, and transmission electron microscopy analyses. ZnO NWs were then employed as heterogeneous and recyclable catalyst for green synthesis of some new and known bispyrazole derivatives through a tandem Knoevenagel and Michael type addition reaction of aromatic aldehyde and pyrazolone. The synthetic method is operationally simple and affords product with high yields in short reaction times.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
4
0

Year Published

2017
2017
2023
2023

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 6 publications
(4 citation statements)
references
References 10 publications
0
4
0
Order By: Relevance
“…The synthetic method is functionally simple, and yield of products are good yields in short reaction time (Scheme 15). [66] In the present work Eskandari et al disclose an expeditious and newer strategy for the condensation of ( 1) with ( 2) in H 2 O/ EtOH and of Mohr's salt as an eco-friendly and predominate, catalyst to give new (3) successfully accomplished via Knoevenagel-Michael reaction. The high efficiency, operational simplicity, minimum reaction time, outstanding yields, high rate, and environmental safety are noticeable advantages of this procedure (Scheme 16).…”
Section: Chemistryselectmentioning
confidence: 87%
See 1 more Smart Citation
“…The synthetic method is functionally simple, and yield of products are good yields in short reaction time (Scheme 15). [66] In the present work Eskandari et al disclose an expeditious and newer strategy for the condensation of ( 1) with ( 2) in H 2 O/ EtOH and of Mohr's salt as an eco-friendly and predominate, catalyst to give new (3) successfully accomplished via Knoevenagel-Michael reaction. The high efficiency, operational simplicity, minimum reaction time, outstanding yields, high rate, and environmental safety are noticeable advantages of this procedure (Scheme 16).…”
Section: Chemistryselectmentioning
confidence: 87%
“…The synthetic method is functionally simple, and yield of products are good yields in short reaction time (Scheme 15). [66] …”
Section: Synthesis Of 44’‐(arylmethylene)‐bis(1‐h‐pyrazol‐5‐ol) Deriv...mentioning
confidence: 99%
“…This transformative chemical reaction culminates in the creation of α,β‐unsaturated compounds through condensing carbonyl‐bearing compounds with those possessing activated methylene [4,5] . The Knoevenagel reaction has lent its prowess to myriad studies, facilitating the synthesis of a diverse array of organic compounds, many of which exhibit compelling biological activities [6–9] …”
Section: Introductionmentioning
confidence: 99%
“…[4,5] The Knoevenagel reaction has lent its prowess to myriad studies, facilitating the synthesis of a diverse array of organic compounds, many of which exhibit compelling biological activities. [6][7][8][9] The profound biological potential of α,β-unsaturated compounds has cast them as captivating molecules, beckoning the interest of chemists and pharmacologists. These compounds have showcased an extensive and diverse spectrum of biological activities, spanning anti-nociception through TREK-1 channel modulation, [10,11] inhibition of 12-Lipoxygenase, [12] acaricidal-fungicidal attributes, [13] antagonism of NMDA receptors, [14] and therapeutic potential for circulatory system diseases.…”
Section: Introductionmentioning
confidence: 99%