C-H functionalization of allenes is an available strategy to construct heterocyclic compounds.Herein we propose a sus-tainable electrocatalytic C-H activation for the synthesis of novel highly functionalized tetrasubs...C-H functionalization of allenes is an available strategy to construct heterocyclic compounds.Herein we propose a sus-tainable electrocatalytic C-H activation for the synthesis of novel highly functionalized tetrasubstituted furans,which is accomplished by intermolecular cyclization of allenes and 1,3-dicarbonyl compounds.展开更多
Correction for‘Electrochemically-mediated C-H functionalization of allenes and 1,3-dicarbonyl compounds to construct tetrasubstituted furans’by Mu-Xue He et al.,Org.Chem.Front.,2022,DOI:10.1039/d1qo01458g.One of the...Correction for‘Electrochemically-mediated C-H functionalization of allenes and 1,3-dicarbonyl compounds to construct tetrasubstituted furans’by Mu-Xue He et al.,Org.Chem.Front.,2022,DOI:10.1039/d1qo01458g.One of the author names(Hai-Tao Tang)was spelled incorrectly in the published article;the corrected version is shown here.The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.展开更多
基金This work was supported by National Natural Science Foundation of China(22161008,21861006,22061003)Guangxi Natural Science Foundation of China(2021GXNSFFA220005)the Chunhui Program(GX2019001).
文摘C-H functionalization of allenes is an available strategy to construct heterocyclic compounds.Herein we propose a sus-tainable electrocatalytic C-H activation for the synthesis of novel highly functionalized tetrasubstituted furans,which is accomplished by intermolecular cyclization of allenes and 1,3-dicarbonyl compounds.
文摘Correction for‘Electrochemically-mediated C-H functionalization of allenes and 1,3-dicarbonyl compounds to construct tetrasubstituted furans’by Mu-Xue He et al.,Org.Chem.Front.,2022,DOI:10.1039/d1qo01458g.One of the author names(Hai-Tao Tang)was spelled incorrectly in the published article;the corrected version is shown here.The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
