Hanan Soliman - Academia.edu (original) (raw)
Papers by Hanan Soliman
Egyptian Journal of Chemistry
ETRACHLOROSILANE/zinc chloride is used as an efficient heterogeneous reagent to promote a one-pot... more ETRACHLOROSILANE/zinc chloride is used as an efficient heterogeneous reagent to promote a one-pot, three component synthesis of γ-Hydroxy-β-ketoamides by the reaction of dimedone, as a 1,3-diketone with various aromatic aldehydes and various nitriles, in dichloromethane at ambient temperature.
Chemical Science Transactions
A green and highly efficient protocol for the one-pot synthesis of a variety of 14-aryl-14-H-dibe... more A green and highly efficient protocol for the one-pot synthesis of a variety of 14-aryl-14-H-dibenzo [a,j]xanthenes and 9-aryl-1,8-dioxo-octahydroxanthenes has been developed via cyclocondensation of aryl aldehydes with 2-naphthol or dimedone using SiO 2-ZnCl 2 (silzic) as a reusable heterogeneous catalyst under solvent-free reaction conditions. In addition, a one-pot, threecomponent condensation of aryl aldehydes, dimedone and ammonium acetate or aryl amines has been developed to furnish 9-aryl-1,8-dioxo-decahydroacridines in good to excellent yields under the same reaction conditions.
Proceedings of The 19th International Electronic Conference on Synthetic Organic Chemistry, 2015
Zeitschrift fur Naturforschung C
A mild method for the regioselective N-bromosuccinimide (NBS) addition to the olefinic double bon... more A mild method for the regioselective N-bromosuccinimide (NBS) addition to the olefinic double bond of benzalmalononitile derivatives using tetrachlorosilane (TCS) in acetonitrile as solvent at room temperature to produce 2-bromo-2-((2,5-dioxopyrrolidin-1-yl)(aryl)methyl) malononitrile, in case of presence of donating group on benzene ring, substitution of â-hydrogen by bromine accrue at the same conditions, also á,â-unsaturated ketones react with TCS/NBS in methylene chloride as a solvent and the corresponding (geminal or vicinal) dibromoketones produced. 2015 Trade Science Inc.-INDIA
Green and efficient MCR protocol for the synthesis of 1,8-dioxo-decahydroacridine derivatives was... more Green and efficient MCR protocol for the synthesis of 1,8-dioxo-decahydroacridine derivatives was achieved through a one-pot, three-component condensation of dimedone, aryl amines and aryl aldehydes utilizing tetrachlorosilane (TCS) as catalyst under solvent-free conditions.
Monatshefte für Chemie - Chemical Monthly, 2015
Zeitschrift für Naturforschung C, 2006
Pyrazolopyranopyrimidines 6a-c and 8a-c were prepared from the reaction of compounds 4a-c or 7a-c... more Pyrazolopyranopyrimidines 6a-c and 8a-c were prepared from the reaction of compounds 4a-c or 7a-c with methylamine or ammonium hydroxide solutions. Treatment of compounds 6a-c or 8a-c with 2-chloroethyl methyl ether afforded their corresponding acyclonucleosides 9a-c or 10a-c, respectively, as a new class of acyclonucleosides. All prepared compounds were tested as anti-inflammatory agents and some of them revealed moderate to potent antiinflammatory activity
Tetrahedron Letters, 1995
Synthesis, structure elucidation qf triazidochlorosilane (TA(~') and a novel conversion of aldehy... more Synthesis, structure elucidation qf triazidochlorosilane (TA(~') and a novel conversion of aldehydes to nitrlles m one pot reaction on treatment with TA('S (Si('I4-NaN 3 in Sitt 0 reagent m acetonitrile are described,
Tetrahedron Letters, 1995
Triazidochlorosilane (SiCl 4 - NaN 3 in situ) is a new and efficient reagent for the direct conve... more Triazidochlorosilane (SiCl 4 - NaN 3 in situ) is a new and efficient reagent for the direct conversion of ketones or α,β-unsaturated ketones to the corresponding tetrazole derivatives in nearly quantitative yield. ... L. Birkhofer and P. Wegner, Chem. Ber. 99 (1966), p. 2512.
Tetrahedron Letters, 1996
A new synthetic procedure for the selective reduction of α,β-unsaturated ketones and nitriles, us... more A new synthetic procedure for the selective reduction of α,β-unsaturated ketones and nitriles, using iodotrichlorosilane (ITCS generated in situ from SiCl 4 -NaI) under mild conditions to produce the corresponding saturated ketone and nitrile compounds in quantitative yields, is ...
Chinese Chemical Letters, 2013
ABSTRACT
Egyptian Journal of Chemistry
ETRACHLOROSILANE/zinc chloride is used as an efficient heterogeneous reagent to promote a one-pot... more ETRACHLOROSILANE/zinc chloride is used as an efficient heterogeneous reagent to promote a one-pot, three component synthesis of γ-Hydroxy-β-ketoamides by the reaction of dimedone, as a 1,3-diketone with various aromatic aldehydes and various nitriles, in dichloromethane at ambient temperature.
Chemical Science Transactions
A green and highly efficient protocol for the one-pot synthesis of a variety of 14-aryl-14-H-dibe... more A green and highly efficient protocol for the one-pot synthesis of a variety of 14-aryl-14-H-dibenzo [a,j]xanthenes and 9-aryl-1,8-dioxo-octahydroxanthenes has been developed via cyclocondensation of aryl aldehydes with 2-naphthol or dimedone using SiO 2-ZnCl 2 (silzic) as a reusable heterogeneous catalyst under solvent-free reaction conditions. In addition, a one-pot, threecomponent condensation of aryl aldehydes, dimedone and ammonium acetate or aryl amines has been developed to furnish 9-aryl-1,8-dioxo-decahydroacridines in good to excellent yields under the same reaction conditions.
Proceedings of The 19th International Electronic Conference on Synthetic Organic Chemistry, 2015
Zeitschrift fur Naturforschung C
A mild method for the regioselective N-bromosuccinimide (NBS) addition to the olefinic double bon... more A mild method for the regioselective N-bromosuccinimide (NBS) addition to the olefinic double bond of benzalmalononitile derivatives using tetrachlorosilane (TCS) in acetonitrile as solvent at room temperature to produce 2-bromo-2-((2,5-dioxopyrrolidin-1-yl)(aryl)methyl) malononitrile, in case of presence of donating group on benzene ring, substitution of â-hydrogen by bromine accrue at the same conditions, also á,â-unsaturated ketones react with TCS/NBS in methylene chloride as a solvent and the corresponding (geminal or vicinal) dibromoketones produced. 2015 Trade Science Inc.-INDIA
Green and efficient MCR protocol for the synthesis of 1,8-dioxo-decahydroacridine derivatives was... more Green and efficient MCR protocol for the synthesis of 1,8-dioxo-decahydroacridine derivatives was achieved through a one-pot, three-component condensation of dimedone, aryl amines and aryl aldehydes utilizing tetrachlorosilane (TCS) as catalyst under solvent-free conditions.
Monatshefte für Chemie - Chemical Monthly, 2015
Zeitschrift für Naturforschung C, 2006
Pyrazolopyranopyrimidines 6a-c and 8a-c were prepared from the reaction of compounds 4a-c or 7a-c... more Pyrazolopyranopyrimidines 6a-c and 8a-c were prepared from the reaction of compounds 4a-c or 7a-c with methylamine or ammonium hydroxide solutions. Treatment of compounds 6a-c or 8a-c with 2-chloroethyl methyl ether afforded their corresponding acyclonucleosides 9a-c or 10a-c, respectively, as a new class of acyclonucleosides. All prepared compounds were tested as anti-inflammatory agents and some of them revealed moderate to potent antiinflammatory activity
Tetrahedron Letters, 1995
Synthesis, structure elucidation qf triazidochlorosilane (TA(~') and a novel conversion of aldehy... more Synthesis, structure elucidation qf triazidochlorosilane (TA(~') and a novel conversion of aldehydes to nitrlles m one pot reaction on treatment with TA('S (Si('I4-NaN 3 in Sitt 0 reagent m acetonitrile are described,
Tetrahedron Letters, 1995
Triazidochlorosilane (SiCl 4 - NaN 3 in situ) is a new and efficient reagent for the direct conve... more Triazidochlorosilane (SiCl 4 - NaN 3 in situ) is a new and efficient reagent for the direct conversion of ketones or α,β-unsaturated ketones to the corresponding tetrazole derivatives in nearly quantitative yield. ... L. Birkhofer and P. Wegner, Chem. Ber. 99 (1966), p. 2512.
Tetrahedron Letters, 1996
A new synthetic procedure for the selective reduction of α,β-unsaturated ketones and nitriles, us... more A new synthetic procedure for the selective reduction of α,β-unsaturated ketones and nitriles, using iodotrichlorosilane (ITCS generated in situ from SiCl 4 -NaI) under mild conditions to produce the corresponding saturated ketone and nitrile compounds in quantitative yields, is ...
Chinese Chemical Letters, 2013
ABSTRACT