ArticleMolecular diversity2010
Synthesis of new tripodal Hantzsch 1,4-dihydropyridines under solvent-free condition and their conversion to the corresponding tripodal pyridines.
Article in Molecular diversity, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed, 17 citations in OpenAlex.
- Corn Stover-Derived Lewis Acid Carbon Catalyst for Efficient Hantzsch Synthesis of 1,4-Dihydropyridines.ACS omega · 2026Article
- An overview on synthetic strategies for the construction of star-shaped molecules.RSC advances · 2019Review
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
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Abstract
A mixture of β-ketoester and tri-aldehydes in the presence of ammonium fluoride was converted to their corresponding tripodal 1,4-dihydropyridines under solvent-free condition with good yields. The obtained tripodal 1,4-dihydropyridines were also aromatized with oxone(®)/NaNO(2)/wet SiO(2) system under mild and heterogeneous conditions quantitatively.
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