Carbonylation of allyl halides catalyzed by poly(N-vinyl-2-pyrro- lidone) anchored palladium catalyst affords β,r-butonic acid under atmo- spheric pressure and at room temperature.The activity and efficiency of the c...Carbonylation of allyl halides catalyzed by poly(N-vinyl-2-pyrro- lidone) anchored palladium catalyst affords β,r-butonic acid under atmo- spheric pressure and at room temperature.The activity and efficiency of the catalyst are much higher than those of the reported catalysts for this reaction.展开更多
Iron-catalyzed direct reduction of allylic halides with benzylic alcohol was achieved,providing a new,simple,and efficient method for conducting highly regioselective hydrodehalogenation.This method not only features ...Iron-catalyzed direct reduction of allylic halides with benzylic alcohol was achieved,providing a new,simple,and efficient method for conducting highly regioselective hydrodehalogenation.This method not only features a readily available reductant,an inexpensive catalyst,simple manipulation,and good tolerance of functional groups including nitriles,nitro,esters,and methoxyl groups,it also has mild reaction conditions and shows complete regioselectivity in that only halides sited at the allylic position are reduced.Alternatively,this method can be applied in the selective transformation of benzylic alcohols to aromatic aldehydes without overoxidation to carboxylic acids.展开更多
A facile preparation of allylic trifluoromethyl thioethers was achieved by using a copper reagent. The reaction of （bpy）Cu（SCF3） with various allylic bromides afforded the desired trifluoromethylthiolation product...A facile preparation of allylic trifluoromethyl thioethers was achieved by using a copper reagent. The reaction of （bpy）Cu（SCF3） with various allylic bromides afforded the desired trifluoromethylthiolation products in good to excellent yields with high stereo- and regioselectivity. Common functional groups such as alkyl, alkoxy, trifluoromethyl, nitro, halides and geranyl are well tolerated.展开更多
文摘Carbonylation of allyl halides catalyzed by poly(N-vinyl-2-pyrro- lidone) anchored palladium catalyst affords β,r-butonic acid under atmo- spheric pressure and at room temperature.The activity and efficiency of the catalyst are much higher than those of the reported catalysts for this reaction.
基金the National Natural Science Foundation of China(21132002&21272038)the National Basic Research Programm of China(973 program,2009CB825300)the Shanghai Leading Academic Discipline Project(B108)for financial support
文摘Iron-catalyzed direct reduction of allylic halides with benzylic alcohol was achieved,providing a new,simple,and efficient method for conducting highly regioselective hydrodehalogenation.This method not only features a readily available reductant,an inexpensive catalyst,simple manipulation,and good tolerance of functional groups including nitriles,nitro,esters,and methoxyl groups,it also has mild reaction conditions and shows complete regioselectivity in that only halides sited at the allylic position are reduced.Alternatively,this method can be applied in the selective transformation of benzylic alcohols to aromatic aldehydes without overoxidation to carboxylic acids.
基金Acknowledgement This work was supported by National Natural Science Foundation of China （No. 21072030）, Research Fund for the Doctoral Program of Higher Education of China （No. 20123514110003）, the Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry （No. 2012-1707）, and Fuzhou University （Nos. 022318, 022494）.
文摘A facile preparation of allylic trifluoromethyl thioethers was achieved by using a copper reagent. The reaction of （bpy）Cu（SCF3） with various allylic bromides afforded the desired trifluoromethylthiolation products in good to excellent yields with high stereo- and regioselectivity. Common functional groups such as alkyl, alkoxy, trifluoromethyl, nitro, halides and geranyl are well tolerated.
