Functionalized alkylzinc iodides will undergo 1,4-conjugation reaction with derivatives of β-nitrostyrene in the presence of Cu(OAc)2/LiCl to afford a polyfunctional nitro-compound in high yield.
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 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Functionalized alkylzinc iodides will undergo 1,4-conjugation reaction with derivatives of β-nitrostyrene in the presence of Cu(OAc)2/LiCl to afford a polyfunctional nitro-compound in high yield.
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.
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.
