Main observation and conclusion A copper-catalyzed radical cyclization of cyclobutanone oxime esters and vinyl azide is described.This method provides facile access to cyanoalkyl-substituted phenanthridines and quinox...Main observation and conclusion A copper-catalyzed radical cyclization of cyclobutanone oxime esters and vinyl azide is described.This method provides facile access to cyanoalkyl-substituted phenanthridines and quinoxalines with excellent isolated yields.Moreover,these reactions proceed under mild conditions with a board substrate scope and excellent functional group tolerance.展开更多
Herein,we report a practical electro-reductive protocol for the direct C-H cyanoalkylation of quinoxalin-2(1 H)-ones via iminyl radical-mediated ring opening.These mild reactions proceed under metal-,reductant-,and re...Herein,we report a practical electro-reductive protocol for the direct C-H cyanoalkylation of quinoxalin-2(1 H)-ones via iminyl radical-mediated ring opening.These mild reactions proceed under metal-,reductant-,and reagent-free conditions to provide synthetically useful cyanoalkylated quinoxalin-2(1 H)-ones.展开更多
An iron-catalyzed coupling reaction of difluoroenol silyl ethers and cyclobutanone oxime esters is described. This protocol provides a convenient access to various previously unknown and potentially useful gem-difluor...An iron-catalyzed coupling reaction of difluoroenol silyl ethers and cyclobutanone oxime esters is described. This protocol provides a convenient access to various previously unknown and potentially useful gem-difluoromethylenated ketonitriles inmoderate to good yields. The transformations of resulting products to other fluorinecontaining products is also documented.展开更多
New blue-light promoted methods for the addition of iodoacetonitrile(ICH_(2)CN)to alkene/alkynes have been developed.The reaction led to the formation of cyanoalkylated products when conjugated alkene/styrene was used...New blue-light promoted methods for the addition of iodoacetonitrile(ICH_(2)CN)to alkene/alkynes have been developed.The reaction led to the formation of cyanoalkylated products when conjugated alkene/styrene was used.In the case of alkynes and non-conjugated alkenes,iodoalkylation takes place furnishing the corresponding alkenyl iodides and alkyl iodides,respectively.Notably,trans-alkenyl iodides were obtained as the major product.A plausible reaction mechanism is also proposed.展开更多
基金We are grateful to the National Natural Science Foundation of China(No.NSFC-21871046).
文摘Main observation and conclusion A copper-catalyzed radical cyclization of cyclobutanone oxime esters and vinyl azide is described.This method provides facile access to cyanoalkyl-substituted phenanthridines and quinoxalines with excellent isolated yields.Moreover,these reactions proceed under mild conditions with a board substrate scope and excellent functional group tolerance.
基金the National Natural Science Foundation of China(Nos.21732002,22077071)Frontiers Science Center for New Organic Matter,Nankai University(No.63181206)for generous financial support for our programs。
文摘Herein,we report a practical electro-reductive protocol for the direct C-H cyanoalkylation of quinoxalin-2(1 H)-ones via iminyl radical-mediated ring opening.These mild reactions proceed under metal-,reductant-,and reagent-free conditions to provide synthetically useful cyanoalkylated quinoxalin-2(1 H)-ones.
基金National Natural Science Foundation of China (Nos.21421002,21991211)the Strategic Priority Research Program of the Chinese Academy of Sciences (No.XDB20000000)。
文摘An iron-catalyzed coupling reaction of difluoroenol silyl ethers and cyclobutanone oxime esters is described. This protocol provides a convenient access to various previously unknown and potentially useful gem-difluoromethylenated ketonitriles inmoderate to good yields. The transformations of resulting products to other fluorinecontaining products is also documented.
基金We are grateful to the National Natural Science Foundation of China(Nos.21961045,22061048)the Yunnan Provincial Key Laboratory Construction Plan Funding of Universities and Yunnan Provincial Engineering Research Center Construction Plan Funding of Universities for their financial support.
文摘New blue-light promoted methods for the addition of iodoacetonitrile(ICH_(2)CN)to alkene/alkynes have been developed.The reaction led to the formation of cyanoalkylated products when conjugated alkene/styrene was used.In the case of alkynes and non-conjugated alkenes,iodoalkylation takes place furnishing the corresponding alkenyl iodides and alkyl iodides,respectively.Notably,trans-alkenyl iodides were obtained as the major product.A plausible reaction mechanism is also proposed.
