Friedel-Crafts alkylation of indoles with nitroalkenes catalyzed by a novel Zn（II）-thiourea complex has been developed. The remarkable advantages of this reaction are mild reaction conditions, simple workup procedur...Friedel-Crafts alkylation of indoles with nitroalkenes catalyzed by a novel Zn（II）-thiourea complex has been developed. The remarkable advantages of this reaction are mild reaction conditions, simple workup procedure, high yield of products and the use of ethanol as acceptable solvent.展开更多
A facile and efficient 1, 4-conjungate addition（Michael addition） reaction of active methylene compounds to aft-unsaturated compounds, catalyzed by guanidinium lactate ionic liquid（IL9）, has been developed. A rang...A facile and efficient 1, 4-conjungate addition（Michael addition） reaction of active methylene compounds to aft-unsaturated compounds, catalyzed by guanidinium lactate ionic liquid（IL9）, has been developed. A range of chalcones and nitroalkenes together with active methylene compounds have been converted smoothly to the corresponding products in high yields.展开更多
A series of new ligands L_1-L_7 were readily prepared in one step.Friedel-Crafts alkylation of indoles with nitroalkenes catalyzed by a novel Cu（Ⅱ）-L complex has been developed.The remarkable advantages of this rea...A series of new ligands L_1-L_7 were readily prepared in one step.Friedel-Crafts alkylation of indoles with nitroalkenes catalyzed by a novel Cu（Ⅱ）-L complex has been developed.The remarkable advantages of this reaction are mild reaction conditions,simple workup procedure,high yields of products and the use of ethanol as a green solvent.展开更多
Intermolecular Stetter reaction of aromatic aldehydes with（E）-（2-nitrovinyl）cyclohexane catalyzed by thiazolium A has been developed.The reaction rate and efficiency are profoundly impacted by the presence of thio...Intermolecular Stetter reaction of aromatic aldehydes with（E）-（2-nitrovinyl）cyclohexane catalyzed by thiazolium A has been developed.The reaction rate and efficiency are profoundly impacted by the presence of thiourea B.The reaction affords moderate to good yields of the Stetter product.Some factors influencing yield were discussed.展开更多
Highly efficient Michael addition reactions of malonates to nitroalkenes catalyzed by novel chiral thioureas derived from optically pure BINOL and amino acids are reported. Various trans-nitroalkenes reacted with malo...Highly efficient Michael addition reactions of malonates to nitroalkenes catalyzed by novel chiral thioureas derived from optically pure BINOL and amino acids are reported. Various trans-nitroalkenes reacted with malonates affording the desired products in up to 95% yield with excellent enantioselectivities （up to 97% ee）.展开更多
Ethylenediamine （H2NCH2CHeNH2） was found to be a highly effective catalyst for the condensation of aryl aldehydes with nitromethane （or nitroethane）. When 1%-2% （tool%） of ethylenediamine was used as the catalys...Ethylenediamine （H2NCH2CHeNH2） was found to be a highly effective catalyst for the condensation of aryl aldehydes with nitromethane （or nitroethane）. When 1%-2% （tool%） of ethylenediamine was used as the catalyst, the one-pot reaction of aryl aldehydes with nitromethane （or nitroethane） by refluxing for 3-10 h efficiently afforded various arylnitroalkenes la-ly in 85%-97% yields.展开更多
Reversal of regioselectivity in the catalytic asymmetric conjugate additions of 3-substituted oxindoles toβ-nitroenones orβ-nitroacrylates was established with chiral scandium catalysts.It enabled the construction o...Reversal of regioselectivity in the catalytic asymmetric conjugate additions of 3-substituted oxindoles toβ-nitroenones orβ-nitroacrylates was established with chiral scandium catalysts.It enabled the construction of functionalized 3,3-disubstituted oxindoles,including terminal and internal vinyl groups in excellent yields and ee values.展开更多
A simple, atom economical and highly efficient green protocol has been developed for the synthesis of Michael adducts of nitroalkenes and 2-amino-2-chromene derivatives by Michael addition of active methylene compoun...A simple, atom economical and highly efficient green protocol has been developed for the synthesis of Michael adducts of nitroalkenes and 2-amino-2-chromene derivatives by Michael addition of active methylene compounds （such as malononitrile and ethyl cyanoacetate） to nitroalkenes under aqueous-mediated conditions. This green approach provided the desired products in high yields and the reaction scope proved to be quite broad.展开更多
Allylindium bromide prepared by metallic indium and allyl bromide was added to nitroalkenes to give conjugate addition compounds in moderate to good yields in an aqueous media.
基金This work was supported by the National Natural Science Foundation of China （Nos. 20962018, 20862015, 20762009 and 20562011）.
文摘Friedel-Crafts alkylation of indoles with nitroalkenes catalyzed by a novel Zn（II）-thiourea complex has been developed. The remarkable advantages of this reaction are mild reaction conditions, simple workup procedure, high yield of products and the use of ethanol as acceptable solvent.
基金Supported by the Jilin University Innovation Fund(No.419070200033).
文摘A facile and efficient 1, 4-conjungate addition（Michael addition） reaction of active methylene compounds to aft-unsaturated compounds, catalyzed by guanidinium lactate ionic liquid（IL9）, has been developed. A range of chalcones and nitroalkenes together with active methylene compounds have been converted smoothly to the corresponding products in high yields.
基金the financial support from the National Natural Science Foundation of China(Nos.20962018, 20862015,20762009 and 20562011)
文摘A series of new ligands L_1-L_7 were readily prepared in one step.Friedel-Crafts alkylation of indoles with nitroalkenes catalyzed by a novel Cu（Ⅱ）-L complex has been developed.The remarkable advantages of this reaction are mild reaction conditions,simple workup procedure,high yields of products and the use of ethanol as a green solvent.
基金supported by the Prospective Research Funds of Jiangsu Provincial Department of Science and Technology (No. BY2015049-02)the Open-end Funds of Jiangsu Key Laboratory of Marine Biotechnology, Huaihai Institute of Technology, (No. 2014HS005)the Funds of Technology Research of Lianyungang (No. CG1301)
文摘Intermolecular Stetter reaction of aromatic aldehydes with（E）-（2-nitrovinyl）cyclohexane catalyzed by thiazolium A has been developed.The reaction rate and efficiency are profoundly impacted by the presence of thiourea B.The reaction affords moderate to good yields of the Stetter product.Some factors influencing yield were discussed.
基金support from Natural Science Foundation of China(No.20772097)Sichuan Provincial Science Foundation for Outstanding Youth(No.05ZQ026-008)Key Project of the Education Department of Sichuan Province(No.2006A081).
文摘Highly efficient Michael addition reactions of malonates to nitroalkenes catalyzed by novel chiral thioureas derived from optically pure BINOL and amino acids are reported. Various trans-nitroalkenes reacted with malonates affording the desired products in up to 95% yield with excellent enantioselectivities （up to 97% ee）.
基金the National Natural Science Foundation of China （No. 20972048） and Shanghai Educational Development Foundation （The Dawn Program： No. 03SG27） for the financial support of this work.
文摘Ethylenediamine （H2NCH2CHeNH2） was found to be a highly effective catalyst for the condensation of aryl aldehydes with nitromethane （or nitroethane）. When 1%-2% （tool%） of ethylenediamine was used as the catalyst, the one-pot reaction of aryl aldehydes with nitromethane （or nitroethane） by refluxing for 3-10 h efficiently afforded various arylnitroalkenes la-ly in 85%-97% yields.
基金financial support from the National Natural Science Foundation of China(No.21890723)。
文摘Reversal of regioselectivity in the catalytic asymmetric conjugate additions of 3-substituted oxindoles toβ-nitroenones orβ-nitroacrylates was established with chiral scandium catalysts.It enabled the construction of functionalized 3,3-disubstituted oxindoles,including terminal and internal vinyl groups in excellent yields and ee values.
文摘A simple, atom economical and highly efficient green protocol has been developed for the synthesis of Michael adducts of nitroalkenes and 2-amino-2-chromene derivatives by Michael addition of active methylene compounds （such as malononitrile and ethyl cyanoacetate） to nitroalkenes under aqueous-mediated conditions. This green approach provided the desired products in high yields and the reaction scope proved to be quite broad.
文摘Allylindium bromide prepared by metallic indium and allyl bromide was added to nitroalkenes to give conjugate addition compounds in moderate to good yields in an aqueous media.
