2012
DOI: 10.1007/s11164-012-0526-9
|View full text |Cite
|
Sign up to set email alerts
|

An efficient and facile synthesis of polydentate ligand: pyridylpyrimidine-2-amine under solvent-free conditions

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2012
2012
2022
2022

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 10 publications
(2 citation statements)
references
References 32 publications
0
2
0
Order By: Relevance
“…[7][8][9][10][11] The eco-friendly, solvent-free multicomponent approach opens up numerous possibilities for environmentally clean synthesis which involves reduction or elimination of the use or generation of hazardous chemicals. [12][13] The possibility of performing multicomponent reactions under solvent-free conditions with a heterogeneous catalyst could improve their cost-effectiveness and ecological acceptability. Nanoparticles exhibit good catalytic activity due to their high surface-to-volume ratio in comparison to their heterogeneous counterparts.…”
Section: Antitubercular Activity (Against Mycobacterium Tuberculosis mentioning
confidence: 99%
“…[7][8][9][10][11] The eco-friendly, solvent-free multicomponent approach opens up numerous possibilities for environmentally clean synthesis which involves reduction or elimination of the use or generation of hazardous chemicals. [12][13] The possibility of performing multicomponent reactions under solvent-free conditions with a heterogeneous catalyst could improve their cost-effectiveness and ecological acceptability. Nanoparticles exhibit good catalytic activity due to their high surface-to-volume ratio in comparison to their heterogeneous counterparts.…”
Section: Antitubercular Activity (Against Mycobacterium Tuberculosis mentioning
confidence: 99%
“…An easy and highly efficient 1-pot reaction for the preparation of 4-aryl-6-(pyridin-2-yl)pyrimidin-2-amine 12 via the reaction of different aromatic aldehydes 4, acetylpyridine 11, and guanidinium carbonate 6 in the presence of NaOH under solvent-free conditions was reported by Tao et al (Scheme 3). 16 Rong et al reported a mild protocol for the synthesis of 4-naphthylpyrimidin-2-amine derivatives 14 (or 16) by the reaction of aromatic aldehydes 4 (or 1-naphthaldehyde 15), 2-acetylnaphthalene 13 (or acetophenones 5) with guanidinium carbonate 6 in the presence of sodium hydroxide under solvent-free conditions (Schemes The heterocyclic pyrido [2,3-d ]pyrimidines ring system represents several biological activities. Some analogues have been found to act as antitumor agents inhibiting dihydrofolate reductases or tyrosine kinases, 20−22 while others are known antiviral agents.…”
Section: Meomentioning
confidence: 99%