An efficient and easy method for one-pot three-component synthesis of l,3-disubstituted-3H-benzo[f]chromenes by the condensation of naphtol,aromatic aldehyde derivatives and phenylacetylene in the presence of ferric h...An efficient and easy method for one-pot three-component synthesis of l,3-disubstituted-3H-benzo[f]chromenes by the condensation of naphtol,aromatic aldehyde derivatives and phenylacetylene in the presence of ferric hydrogensulfate[Fe（HSO4）3], has been described.The catalyst displayed high activity which afforded the corresponding 1,3-disubstituted-3H-benzo[f]chromenes in satisfying yields.Alkyl-substituted phenols were examined and the corresponding benzopyran derivatives were synthesized in moderate yields.Heterogeneous nature of the using catalyst made it reusable for further chemical reactions.展开更多
The symmetric oxidative coupling reactions of 2-naphthol derivatives with both ferric hydrogensulfate in water and silica ferric hydrogensulfate in solvent free conditions were carried out. The advantages of this gree...The symmetric oxidative coupling reactions of 2-naphthol derivatives with both ferric hydrogensulfate in water and silica ferric hydrogensulfate in solvent free conditions were carried out. The advantages of this green procedure are inexpensive catalyst or cocatalyst, reusability of catalyst, organic solvent-free procedures and simple workup.展开更多
Efficient reaction of bis-indolyl podand with different aldehydes using Fe（HSO4）3 as catalyst to afford the corresponding new indolyl crown ethers is described. The structures of three distinct isomers have been opt...Efficient reaction of bis-indolyl podand with different aldehydes using Fe（HSO4）3 as catalyst to afford the corresponding new indolyl crown ethers is described. The structures of three distinct isomers have been optimized using HyperChem geometry optimizations. Also percentage of each isomer was obtained with 1H NMR spectroscopy.展开更多
We have demonstrated the direct substitution of 9H-xanthen-9-ol with different nucleophilic reagents such as thiazoles, triazoles, tetrazoles, hydrazines and hydrazinecarboxamides in good to high yields. This reaction...We have demonstrated the direct substitution of 9H-xanthen-9-ol with different nucleophilic reagents such as thiazoles, triazoles, tetrazoles, hydrazines and hydrazinecarboxamides in good to high yields. This reaction catalyzed by ferric hydro- gensulfate as a heterogeneous acid catalyst in ethanol through SN1 type reaction of pyrylium with a nucleophilic reagent afforded the heterocycle- and aromatic-N-substituted xanthene derivatives as simple marked molecules in short reaction times.展开更多
文摘An efficient and easy method for one-pot three-component synthesis of l,3-disubstituted-3H-benzo[f]chromenes by the condensation of naphtol,aromatic aldehyde derivatives and phenylacetylene in the presence of ferric hydrogensulfate[Fe（HSO4）3], has been described.The catalyst displayed high activity which afforded the corresponding 1,3-disubstituted-3H-benzo[f]chromenes in satisfying yields.Alkyl-substituted phenols were examined and the corresponding benzopyran derivatives were synthesized in moderate yields.Heterogeneous nature of the using catalyst made it reusable for further chemical reactions.
文摘The symmetric oxidative coupling reactions of 2-naphthol derivatives with both ferric hydrogensulfate in water and silica ferric hydrogensulfate in solvent free conditions were carried out. The advantages of this green procedure are inexpensive catalyst or cocatalyst, reusability of catalyst, organic solvent-free procedures and simple workup.
文摘Efficient reaction of bis-indolyl podand with different aldehydes using Fe（HSO4）3 as catalyst to afford the corresponding new indolyl crown ethers is described. The structures of three distinct isomers have been optimized using HyperChem geometry optimizations. Also percentage of each isomer was obtained with 1H NMR spectroscopy.
基金Department of Chemistry,Ferdowsi University of Mashhad,for financial support(49-P-24-01- 89)
文摘We have demonstrated the direct substitution of 9H-xanthen-9-ol with different nucleophilic reagents such as thiazoles, triazoles, tetrazoles, hydrazines and hydrazinecarboxamides in good to high yields. This reaction catalyzed by ferric hydro- gensulfate as a heterogeneous acid catalyst in ethanol through SN1 type reaction of pyrylium with a nucleophilic reagent afforded the heterocycle- and aromatic-N-substituted xanthene derivatives as simple marked molecules in short reaction times.
