2005
DOI: 10.1016/j.catcom.2005.07.012
|View full text |Cite
|
Sign up to set email alerts
|

Amino group immobilized on polyacrylamide: An efficient heterogeneous catalyst for the Knoevenagel reaction in solvent-free and aqueous media

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
18
0

Year Published

2010
2010
2023
2023

Publication Types

Select...
9
1

Relationship

0
10

Authors

Journals

citations
Cited by 57 publications
(18 citation statements)
references
References 26 publications
(30 reference statements)
0
18
0
Order By: Relevance
“…This reaction produces several important key products that include nitriles used in anionic polymerisation and the α,β-unsaturated ester intermediates employed in the synthesis of several therapeutic drugs and pharmacological products. 10,11 Several types of catalysts were introduced previously for Knoevenagel condensation such as the weak bases ammonia, primary amine and secondary amines and their salts, 12,13 16 LaCl 3 , 17 non-cross-linked polystyrene-supported piperazine, 18 zeolite, 19 amino group immobilised on polyacrylamide, 20 SiO 2 -HClO 4 and SiO 2 -PPA, 21 amine functionalised MCM-41, 22 ionic liquids, 23−25 silica based substituted piperidine, 26 and amino functionalised mesoporous silica. 27 However, many of the reported catalysts suffer from drawbacks such as generation of environmentally perilous waste material, tedious work-up, long reaction times, complicated operations, and the use of * Correspondent.…”
mentioning
confidence: 99%
“…This reaction produces several important key products that include nitriles used in anionic polymerisation and the α,β-unsaturated ester intermediates employed in the synthesis of several therapeutic drugs and pharmacological products. 10,11 Several types of catalysts were introduced previously for Knoevenagel condensation such as the weak bases ammonia, primary amine and secondary amines and their salts, 12,13 16 LaCl 3 , 17 non-cross-linked polystyrene-supported piperazine, 18 zeolite, 19 amino group immobilised on polyacrylamide, 20 SiO 2 -HClO 4 and SiO 2 -PPA, 21 amine functionalised MCM-41, 22 ionic liquids, 23−25 silica based substituted piperidine, 26 and amino functionalised mesoporous silica. 27 However, many of the reported catalysts suffer from drawbacks such as generation of environmentally perilous waste material, tedious work-up, long reaction times, complicated operations, and the use of * Correspondent.…”
mentioning
confidence: 99%
“…In general, the Knoevenagel condensation is carried out in the presence of different catalysts, including carbonyl compounds, aldehydes or ketones, and active methylene compounds. Lewis acid catalysts such as LaCl 3 (Narsaiah and Nagaiah, 2003 ), piperidine and alkali metal supported catalysts (Leelavathi and Kumar, 2004 ; Martín-Aranda et al, 2005 ; Perozo-Rondon et al, 2006 ), ionic liquids (Moriel et al, 2010 ), or alkali modified metal oxides (Calvino-Casilda et al, 2009 ), zeolites (Wada and Suzuki, 2003 ) and mesoporous materials (Zienkiewicz et al, 2009 ) or polymer-supported catalysts (Tamami and Fadavi, 2005 ) were used as catalysts.…”
Section: Catalysis On Niobium-containing Mesoporous Silicatesmentioning
confidence: 99%
“…(Scheme -09) Tamami B. and Fadavi A. [24] have synthesized the malononitrile derivatives 24 in presence of modified form of polyacrylamide catalyst heated under water by using equimolar mixture of aromatic aldehyde 22 and nitrile 23 analogs. Lin Q. et al [25] have designed a novel chemosensor of cyanide analogous 26 by the condensation between napthaldehyde 25 with mlononitrile 1 heated at 90°C fro 2 hrs in aqueous media via green synthesis.…”
Section: Methods Of Synthesis Of Malononitrilementioning
confidence: 99%