A new method for the cleavage of carbohydrate benzylidene acetal has been developed using Ceric (YV) ammonium nitrate (CAN) [(NH4)2Ce(NO3)6] in CH3CN-H2O (10/1, v/v).
An efficient one-pot synthesis of 2,4,6-triarylpyridines has been described.This involves the three-component reaction of aldehydes,ketones and ammonium acetate in the presence of a catalytic amount of wet 2,4,6-trich...An efficient one-pot synthesis of 2,4,6-triarylpyridines has been described.This involves the three-component reaction of aldehydes,ketones and ammonium acetate in the presence of a catalytic amount of wet 2,4,6-trichloro-1,3,5-triazine(TCT) under solvent-free condition at 130℃.展开更多
A simple and efficient method has been developed;benzil/benzoin undergoes smooth condensation with various substituted aldehyde and ammonium acetate in the presence of potassium dihydrogen phosphate(KH;PO;) under mi...A simple and efficient method has been developed;benzil/benzoin undergoes smooth condensation with various substituted aldehyde and ammonium acetate in the presence of potassium dihydrogen phosphate(KH;PO;) under mild reaction conditions to afford the corresponding trisubstituted imidazole in excellent yields.The method for synthesis of product,the reaction mixture was reflux in ethanol for 40-90 min.The present method is simple,efficient,and cost-effective.展开更多
A simple one-pot synthetic method for the preparation of 2,4,5-triaryl-lH-imidazoles from benzoin or benzil, ammonium acetate, aromatic aldehydes, and ZrOCl2-8H2O catalyst is described. The ZrOCl2-8H2O catalyst was fo...A simple one-pot synthetic method for the preparation of 2,4,5-triaryl-lH-imidazoles from benzoin or benzil, ammonium acetate, aromatic aldehydes, and ZrOCl2-8H2O catalyst is described. The ZrOCl2-8H2O catalyst was found to be equally effective for aromatic and heteroaromatic aldehydes and also for the preparation of substituted 1,4-di(4,5-diphenylimidazol-yl) benzene.展开更多
The Co(II) complex I and ammonium salt II were synthesized from the direct reaction of 1,2-ethylenediamine and cobaltous acetate tetrahydrate and manganese acetate tetrahydrate in anhydrous ethanol. Treatment of N,N...The Co(II) complex I and ammonium salt II were synthesized from the direct reaction of 1,2-ethylenediamine and cobaltous acetate tetrahydrate and manganese acetate tetrahydrate in anhydrous ethanol. Treatment of N,N'-bis(salicylidene)ethylenediamine with Cu(OAc)2·H2O results in the formation of Cu(II) complex III. C14H37CoNaO8 (I): triclinic, space group P1, a = 8.6296(12), b = 12.0291(17), c = 12.1108(17) A, α = 75.335(2), β = 69.991(2), γ = 72.248(2)°, V= 1109.4(3) A3, Z = 2, ρcaloa = 1.342 g/cm3, the final R= 0.0342 for 4817 observed reflections with I 〉 2σ(I) and Rw = 0.1263 for all data. C6H16N204 (II): space group P1, a = 5.5513(10), b = 5.5589(11), c = 7.4437(14) A, α = 94.332(4), β = 104.497(4), γ = 103.487(4)°,V= 214.06(7) A3, Z = 1, ρcalcd = 1.398 g/cm3, the final R = 0.0431 for 829 observed reflections with I〉 2σ(I) and Rw = 0.1263 for all data. C14H37CuN40 (III), space group P21/n, a = 9.050(9), b = 18.434(17), c = 11.659(11) A, β = 107.134(19)°, V= 1859(3) A3, Z = 4, ρcalcd =1.443 g/cm3, the final R = 0.0616 for 3308 observed reflections (O 〉 2σ(I)) and Rw = 0.1229 for all data. Their structures were all determined by X-ray diffraction, elemental analysis and IR.展开更多
In order to quantitate dencichine in biological samples, a selective and sensitive method for the determination of dencichine in rat plasma based on high-performance liquid chromatography-tandem mass spectrometry (HPL...In order to quantitate dencichine in biological samples, a selective and sensitive method for the determination of dencichine in rat plasma based on high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was developed and validated. (l)-2-amino-3-(carboxymethylthio)propionic acid was used as the internal standard (I.S.). After a protein precipitation extraction with acetonitrile, dencichine and the I.S. were chromatographed on an Xterra MS-C18 column. The mobile phase was consisted of 20mmol/L ammonium acetate solution-acetonitrile (35:65, V/V) at a flow rate of 0.2 mL/min. The detection was performed on a triple quadrupole mass via electrospray ionization (ESI) source in the positive mode. The intra- and inter-day precision (relative standard deviation, R.S.D.) values of dencichine were below 6.7%. The extraction recoveries were up 85%. The lower limit of quantification was 20 ng/ml, which was sensitive enough to detect the analyte. The HPLC-MS/MS method was successfully applied to the pharmacokinetic study after an intravenous administration of dencichine in Sprague-Dawley (SD) rat.展开更多
Various 2-phenylimidazo [4,5-f] [1,10] phenanthrolines were synthesized from potassium ferro-cyanide trihydrate (KFCT) complex catalyzed three component reaction of 1,10-phenanthroline-5,6-dione, aromatic aldehydes ...Various 2-phenylimidazo [4,5-f] [1,10] phenanthrolines were synthesized from potassium ferro-cyanide trihydrate (KFCT) complex catalyzed three component reaction of 1,10-phenanthroline-5,6-dione, aromatic aldehydes and ammonium acetate at room temperature in excellent isolated yield. This is a simple and straight forward, high yielding, not involving any hazardous or expensive catalyst method.展开更多
A facile synthesis of benzofuro[2,3-c]pyridines has been achieved under mild conditions by using ammonium acetate as the nitrogen source through intramolecular cascade annulation.This reaction could efficiently constr...A facile synthesis of benzofuro[2,3-c]pyridines has been achieved under mild conditions by using ammonium acetate as the nitrogen source through intramolecular cascade annulation.This reaction could efficiently construct pyridine ring and furan ring in one step.Moreover,the key annulation step was demonstrated through dihydrobenzofuran intermediates.展开更多
文摘A new method for the cleavage of carbohydrate benzylidene acetal has been developed using Ceric (YV) ammonium nitrate (CAN) [(NH4)2Ce(NO3)6] in CH3CN-H2O (10/1, v/v).
文摘An efficient one-pot synthesis of 2,4,6-triarylpyridines has been described.This involves the three-component reaction of aldehydes,ketones and ammonium acetate in the presence of a catalytic amount of wet 2,4,6-trichloro-1,3,5-triazine(TCT) under solvent-free condition at 130℃.
文摘A simple and efficient method has been developed;benzil/benzoin undergoes smooth condensation with various substituted aldehyde and ammonium acetate in the presence of potassium dihydrogen phosphate(KH;PO;) under mild reaction conditions to afford the corresponding trisubstituted imidazole in excellent yields.The method for synthesis of product,the reaction mixture was reflux in ethanol for 40-90 min.The present method is simple,efficient,and cost-effective.
文摘A simple one-pot synthetic method for the preparation of 2,4,5-triaryl-lH-imidazoles from benzoin or benzil, ammonium acetate, aromatic aldehydes, and ZrOCl2-8H2O catalyst is described. The ZrOCl2-8H2O catalyst was found to be equally effective for aromatic and heteroaromatic aldehydes and also for the preparation of substituted 1,4-di(4,5-diphenylimidazol-yl) benzene.
文摘The Co(II) complex I and ammonium salt II were synthesized from the direct reaction of 1,2-ethylenediamine and cobaltous acetate tetrahydrate and manganese acetate tetrahydrate in anhydrous ethanol. Treatment of N,N'-bis(salicylidene)ethylenediamine with Cu(OAc)2·H2O results in the formation of Cu(II) complex III. C14H37CoNaO8 (I): triclinic, space group P1, a = 8.6296(12), b = 12.0291(17), c = 12.1108(17) A, α = 75.335(2), β = 69.991(2), γ = 72.248(2)°, V= 1109.4(3) A3, Z = 2, ρcaloa = 1.342 g/cm3, the final R= 0.0342 for 4817 observed reflections with I 〉 2σ(I) and Rw = 0.1263 for all data. C6H16N204 (II): space group P1, a = 5.5513(10), b = 5.5589(11), c = 7.4437(14) A, α = 94.332(4), β = 104.497(4), γ = 103.487(4)°,V= 214.06(7) A3, Z = 1, ρcalcd = 1.398 g/cm3, the final R = 0.0431 for 829 observed reflections with I〉 2σ(I) and Rw = 0.1263 for all data. C14H37CuN40 (III), space group P21/n, a = 9.050(9), b = 18.434(17), c = 11.659(11) A, β = 107.134(19)°, V= 1859(3) A3, Z = 4, ρcalcd =1.443 g/cm3, the final R = 0.0616 for 3308 observed reflections (O 〉 2σ(I)) and Rw = 0.1229 for all data. Their structures were all determined by X-ray diffraction, elemental analysis and IR.
文摘In order to quantitate dencichine in biological samples, a selective and sensitive method for the determination of dencichine in rat plasma based on high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was developed and validated. (l)-2-amino-3-(carboxymethylthio)propionic acid was used as the internal standard (I.S.). After a protein precipitation extraction with acetonitrile, dencichine and the I.S. were chromatographed on an Xterra MS-C18 column. The mobile phase was consisted of 20mmol/L ammonium acetate solution-acetonitrile (35:65, V/V) at a flow rate of 0.2 mL/min. The detection was performed on a triple quadrupole mass via electrospray ionization (ESI) source in the positive mode. The intra- and inter-day precision (relative standard deviation, R.S.D.) values of dencichine were below 6.7%. The extraction recoveries were up 85%. The lower limit of quantification was 20 ng/ml, which was sensitive enough to detect the analyte. The HPLC-MS/MS method was successfully applied to the pharmacokinetic study after an intravenous administration of dencichine in Sprague-Dawley (SD) rat.
文摘Various 2-phenylimidazo [4,5-f] [1,10] phenanthrolines were synthesized from potassium ferro-cyanide trihydrate (KFCT) complex catalyzed three component reaction of 1,10-phenanthroline-5,6-dione, aromatic aldehydes and ammonium acetate at room temperature in excellent isolated yield. This is a simple and straight forward, high yielding, not involving any hazardous or expensive catalyst method.
基金This work was financially supported by the Natural Science Foundation of Henan Province(No.132300410319)and Luoyang Normal University.
文摘A facile synthesis of benzofuro[2,3-c]pyridines has been achieved under mild conditions by using ammonium acetate as the nitrogen source through intramolecular cascade annulation.This reaction could efficiently construct pyridine ring and furan ring in one step.Moreover,the key annulation step was demonstrated through dihydrobenzofuran intermediates.