A new rapid synthetic method is described for synthesis of a, a-dibenzylidene- cycloalkanones by the reaction of acetals and cycloalkanones without solvent using BF3稥t2O as catalyst under microwave irradiation.
Functionalized organozinc reagents can easily under 1, 4-addition reaction withunsaturated esters in the presence of catalytic amount of Ni (acac)_2 and tertiary ammes under verymild conditions to give the products in...Functionalized organozinc reagents can easily under 1, 4-addition reaction withunsaturated esters in the presence of catalytic amount of Ni (acac)_2 and tertiary ammes under verymild conditions to give the products in excellent yields.展开更多
Functionalized benzylic zinc halides reacted with benzaldehydes in the presence of Lewis acid Me3SiCl giving high yields of trans-stilbenes under the catalysis of Co(PPh3)3Cl.
A method for selective reaction of 1-aryl-propane-1-ones with 1,2-dihydrxy grop of D-mannitol in the presence of ZnCl2-BF3 Et2O to 1, 2_O-(1-aryl- propylidene )-D-mannitol (1-4 ) is described. The compounds were first...A method for selective reaction of 1-aryl-propane-1-ones with 1,2-dihydrxy grop of D-mannitol in the presence of ZnCl2-BF3 Et2O to 1, 2_O-(1-aryl- propylidene )-D-mannitol (1-4 ) is described. The compounds were first reported and determined by IR, MS, 1H-/13C-NMR spectra.among them the Shae of 1 was further defined by X-ray diffraction展开更多
Functionalized organozinc reagents can easily conduct 1,4-addition reaction with unsaturated esters in the presence of Cu(OAc)2 and LiCl under very Anld conditions to give the products in excellent yields.
基金The work was supported by the National Natural Science Foundation of China (NO. 20272047) and the Northwest Normal University Science and Technology Development Foundation of China.
文摘A new rapid synthetic method is described for synthesis of a, a-dibenzylidene- cycloalkanones by the reaction of acetals and cycloalkanones without solvent using BF3稥t2O as catalyst under microwave irradiation.
文摘Functionalized organozinc reagents can easily under 1, 4-addition reaction withunsaturated esters in the presence of catalytic amount of Ni (acac)_2 and tertiary ammes under verymild conditions to give the products in excellent yields.
基金supported by the National Natural Science Foundation of China(No.20472068)Specialized Research Fund for the Doctoral Program of Higher Education(No.200807360001)Key Laboratory of Eco-Environment -Related Polymer Materials of Ministry of Education(Northwest Normal University)
文摘2,5-Disubstituted tetrahydrofurans were obtained from lactones and organozinc halides in moderate to high yield in the presence of Lewis acids.
基金This work was supported by the National Natural Science Foundation of China and the Northwest Normal University Science and Technology Devolopment Foundation of China.
文摘Functionalized benzylic zinc halides reacted with benzaldehydes in the presence of Lewis acid Me3SiCl giving high yields of trans-stilbenes under the catalysis of Co(PPh3)3Cl.
文摘A method for selective reaction of 1-aryl-propane-1-ones with 1,2-dihydrxy grop of D-mannitol in the presence of ZnCl2-BF3 Et2O to 1, 2_O-(1-aryl- propylidene )-D-mannitol (1-4 ) is described. The compounds were first reported and determined by IR, MS, 1H-/13C-NMR spectra.among them the Shae of 1 was further defined by X-ray diffraction
文摘Functionalized organozinc reagents can easily conduct 1,4-addition reaction with unsaturated esters in the presence of Cu(OAc)2 and LiCl under very Anld conditions to give the products in excellent yields.
