Sulphamic acid （H2NSO3H） was found to be an efficient catalyst for the multicomponent condensation reaction of β-naphthol, aromatic aldehydes and urea or amides to afford the corresponding α-amidoalkyl-β-naphthol...Sulphamic acid （H2NSO3H） was found to be an efficient catalyst for the multicomponent condensation reaction of β-naphthol, aromatic aldehydes and urea or amides to afford the corresponding α-amidoalkyl-β-naphthols in good yields. The remarkable features of this new procedure are high conversions, short reaction time, clean reaction profiles and simple experimental and work-up procedures.展开更多
Ammonium metavanadate （10 mol%） was found to be a useful catalyst for the synthesis of various 2-substituted aryl benzimidazoles. It was used as an oxidizing agent for the condensation of o-phenylenediamine with dif...Ammonium metavanadate （10 mol%） was found to be a useful catalyst for the synthesis of various 2-substituted aryl benzimidazoles. It was used as an oxidizing agent for the condensation of o-phenylenediamine with different substituted aryl aldehydes at room temperature in ethanol. The method was proved to be simple, convenient and the product was isolated with good yields （79-91%）.展开更多
α-Aryl nitrone are one of the most useful kinds of nitrones and have been extensively explored in recent years.However,the sugar moieties have not been introduced into these molecules before.We presented here an effi...α-Aryl nitrone are one of the most useful kinds of nitrones and have been extensively explored in recent years.However,the sugar moieties have not been introduced into these molecules before.We presented here an efficient synthesis ofα-aryl nitrone Oglycosides via condensation of N-substituted hydroxylamine and aryl aldehydes glycosides in benzene.展开更多
Nine 10-arylidene anthrones were synthesized from anthrone and aryl aldehydes in xylene using pyridine as catalyst and p-t-butylphenol as an antioxidant. The higher yields of the nine title compounds were achieved due...Nine 10-arylidene anthrones were synthesized from anthrone and aryl aldehydes in xylene using pyridine as catalyst and p-t-butylphenol as an antioxidant. The higher yields of the nine title compounds were achieved due to adding p-t-butylphenol in the reaction system which could significantly avoid formation of anthraquinone, the main by-product of the reaction, leading a troublesome procedure for product purification.展开更多
Synthesis of 2-aryl-1-arylmethyl-1H-1,3-benzo[d]imidazoles by the reaction of o-phenylenediamine with substituted aromatic aldehydes in the presence of 1-heptanesulfonic acid sodium salt （10 mol%） at room temperatur...Synthesis of 2-aryl-1-arylmethyl-1H-1,3-benzo[d]imidazoles by the reaction of o-phenylenediamine with substituted aromatic aldehydes in the presence of 1-heptanesulfonic acid sodium salt （10 mol%） at room temperature. The reactions were performed in acetonitrile：water （8：2）. The method was proved to be eco-friendly, convenient and the products were isolated with good yields （82- 90%）.展开更多
Under esterification conditions, 2-(1,2-ethylenedithio) methylene-3-oxo-5-aryl-4-pentenoic acid 3 afforded the decarboxylated products 4. The triphenyltin 2-(1, 2-ethylenedithio) methylene-3-oxo-5-aryl-4-pentenoates 5...Under esterification conditions, 2-(1,2-ethylenedithio) methylene-3-oxo-5-aryl-4-pentenoic acid 3 afforded the decarboxylated products 4. The triphenyltin 2-(1, 2-ethylenedithio) methylene-3-oxo-5-aryl-4-pentenoates 5 were obtained in high yields when 3 reacted with triphenyltin hydroxide.展开更多
文摘Sulphamic acid （H2NSO3H） was found to be an efficient catalyst for the multicomponent condensation reaction of β-naphthol, aromatic aldehydes and urea or amides to afford the corresponding α-amidoalkyl-β-naphthols in good yields. The remarkable features of this new procedure are high conversions, short reaction time, clean reaction profiles and simple experimental and work-up procedures.
文摘Ammonium metavanadate （10 mol%） was found to be a useful catalyst for the synthesis of various 2-substituted aryl benzimidazoles. It was used as an oxidizing agent for the condensation of o-phenylenediamine with different substituted aryl aldehydes at room temperature in ethanol. The method was proved to be simple, convenient and the product was isolated with good yields （79-91%）.
基金support from National Natural Science Foundation of China(No.20962017) the Natural Science Foundation of Gansu Province,China(No.2007GS03630)
文摘α-Aryl nitrone are one of the most useful kinds of nitrones and have been extensively explored in recent years.However,the sugar moieties have not been introduced into these molecules before.We presented here an efficient synthesis ofα-aryl nitrone Oglycosides via condensation of N-substituted hydroxylamine and aryl aldehydes glycosides in benzene.
文摘Nine 10-arylidene anthrones were synthesized from anthrone and aryl aldehydes in xylene using pyridine as catalyst and p-t-butylphenol as an antioxidant. The higher yields of the nine title compounds were achieved due to adding p-t-butylphenol in the reaction system which could significantly avoid formation of anthraquinone, the main by-product of the reaction, leading a troublesome procedure for product purification.
文摘Synthesis of 2-aryl-1-arylmethyl-1H-1,3-benzo[d]imidazoles by the reaction of o-phenylenediamine with substituted aromatic aldehydes in the presence of 1-heptanesulfonic acid sodium salt （10 mol%） at room temperature. The reactions were performed in acetonitrile：water （8：2）. The method was proved to be eco-friendly, convenient and the products were isolated with good yields （82- 90%）.
文摘Under esterification conditions, 2-(1,2-ethylenedithio) methylene-3-oxo-5-aryl-4-pentenoic acid 3 afforded the decarboxylated products 4. The triphenyltin 2-(1, 2-ethylenedithio) methylene-3-oxo-5-aryl-4-pentenoates 5 were obtained in high yields when 3 reacted with triphenyltin hydroxide.
