Highly regioselective homocoupling of N,N-dialkylanilines can be achieved in water with cerium reagents, in which various N,N,N′,N′-tetraalkylbenzidines are obtained from N,N-dialkylanilines either by direct oxidati...Highly regioselective homocoupling of N,N-dialkylanilines can be achieved in water with cerium reagents, in which various N,N,N′,N′-tetraalkylbenzidines are obtained from N,N-dialkylanilines either by direct oxidation by cerium(Ⅳ)reagents or by cerium(Ⅲ) reagents in the presence of hydroperoxide.展开更多
Homocoupling of aryl iodides catalyzed by cyclopalladated complexes of tertiary arylamines gives symmetric biaryls with good yields in DMA or ionic liquid [Bmim]BF4. This catalytic alternative of the Ullmann reaction ...Homocoupling of aryl iodides catalyzed by cyclopalladated complexes of tertiary arylamines gives symmetric biaryls with good yields in DMA or ionic liquid [Bmim]BF4. This catalytic alternative of the Ullmann reaction has proved to be sensitive to both electronic and steric factors of substrates.展开更多
Pyridine was used as a solvent for homocoupling of aryl bromides catalyzed by nickel chloride/triarylphosphine in the presence of zinc and recycled easily. Triphenylphosphine was the best ligand for nickel in this cou...Pyridine was used as a solvent for homocoupling of aryl bromides catalyzed by nickel chloride/triarylphosphine in the presence of zinc and recycled easily. Triphenylphosphine was the best ligand for nickel in this coupling reaction.展开更多
Herein,we describe an environmentally benign and cost.efective protocol for the synthesis of valuable bifuranyl dicarboylates,starting with a-bromination of readily accessible furan-2-carboylates by LiBr and K_(2)S_(2...Herein,we describe an environmentally benign and cost.efective protocol for the synthesis of valuable bifuranyl dicarboylates,starting with a-bromination of readily accessible furan-2-carboylates by LiBr and K_(2)S_(2)O_(8).Furthermore,the bromination intermediate product 5-bromofuran-2-carboxylates were then conducted in a palladium-catalyzed reductive homocoupling reactions in the pres-ence of alcohols to afford bifuranyl dicarboxylates.One of the final products in this protocol,[2,2']bifuran-5,5'-dicarboxylic acid es-ters,are essential monomers of poly(ethylene bifuranoate),which can be served as an green and versatile alternative polymer for traditional poly(ethylene terephthalate)that is currently common in technical plastics.展开更多
Pd-catalyzed oxidative homocoupling of 2-arylquinazolinones was successfully developed for the direct construction of biaryls via C—H bond activation.New well-defined structure that possessed two quinazolinone units ...Pd-catalyzed oxidative homocoupling of 2-arylquinazolinones was successfully developed for the direct construction of biaryls via C—H bond activation.New well-defined structure that possessed two quinazolinone units was obtained with high efficiency and atomic economy.The protocols offer an efficient approach to the synthetically useful and functionalized biaryls in good yields using quinazolinone as a directing group.展开更多
A new homocoupling methodology mediated by a novel combination of CuCl-2,2'-dipyridyl and its application to the synthesis of substituted polyfluorinated alka-2,4-dienes are described.
Photosensitizing supramolecular assemblies based on a phenazine derivative(PPA)have been developed,which show a strong affinity toward Pd2+ions to generate supramolecular ensemble PPA@Pd nanoparticles(NPs).The PPA@Pd ...Photosensitizing supramolecular assemblies based on a phenazine derivative(PPA)have been developed,which show a strong affinity toward Pd2+ions to generate supramolecular ensemble PPA@Pd nanoparticles(NPs).The PPA@Pd NPs catalyse the Suzuki cross-coupled reaction under mild conditions(aerial conditions,mixed aqueous media,and visible light radiations).Although PPA@Pd NPs exhibit a strong affinity for arylboronic acid and could catalyse homocoupling of arylboronic acid,the preference of PPA assemblies for aryl halide directed the course of reactions toward the formation of cross-coupled products.The electron-rich PPA assemblies not only facilitate the oxidative addition step through photoinduced electron transfer to Pd^(2+)ions but also bring the reactants closer to the catalytic sites by selective interactions with aryl halides in the presence of arylboronic acid under visible light irradiation.The efficiency of PPA@Pd NPs to catalyse the Suzuki crosscoupled reaction has been demonstrated for the synthesis of unsymmetrically substituted terphenyl derivatives.展开更多
Symmetrical diynes were synthesized by ligand-free copper-catalyzed homocoupling reaction of 1,1-dibromo-1- alkenes using a DBU/DMSO system at room temperature in good to excellent yields.
Copper/oxalic diamide-promoted dimerization of tetrachlorinated perylene bisimide to construct highly-fused diperylene bisimides through Ullmann coupling and zipper-mode double C—H activation has been developed in th...Copper/oxalic diamide-promoted dimerization of tetrachlorinated perylene bisimide to construct highly-fused diperylene bisimides through Ullmann coupling and zipper-mode double C—H activation has been developed in this study.This one-step reaction combining homocoupling with C—H activation proceeded smoothly under the action of inexpensive metal-ligand system.This protocol is expected to expand the available synthetic tools for condensed ring systems of perylene bisimide(PBIs).展开更多
We present the mechanistic understanding of an electrochemically-driven nickel-catalyzed coupling reaction.Computational analysis reveals that the spin density is mostly residing on the nickel(Ni)center when Ni^(II) i...We present the mechanistic understanding of an electrochemically-driven nickel-catalyzed coupling reaction.Computational analysis reveals that the spin density is mostly residing on the nickel(Ni)center when Ni^(II) is reduced to NiI.Ni-mediated halogen atom abstraction through outer-sphere electron-transfer pathway to yield coupling products under mild conditions is demonstrated.Importantly,we have elucidated the role of Ni^(I) and Ni^(0) for successive coupling of benzyl bromide and benzyl chloride derivatives,respectively,to corresponding bibenzyl products.The Ni-catalyst bearing a PN^(3) P-ligand is an effective catalyst,producing a strong ligand effect on the reactivity and selectivity for the homocoupling reactions.展开更多
基金Supported by the National Natural Science Foundation of China(Nos20572058 and 20372041)Beijing Department of Education(NoXK100030514)
文摘Highly regioselective homocoupling of N,N-dialkylanilines can be achieved in water with cerium reagents, in which various N,N,N′,N′-tetraalkylbenzidines are obtained from N,N-dialkylanilines either by direct oxidation by cerium(Ⅳ)reagents or by cerium(Ⅲ) reagents in the presence of hydroperoxide.
基金Project supported by the National Natural Science Foundation of China (No. 20172016) and Shanghai Phosphor Project of Science & Technology for Excellent Young Research (Nos. 01QA14017 and 02QA14016).
文摘Homocoupling of aryl iodides catalyzed by cyclopalladated complexes of tertiary arylamines gives symmetric biaryls with good yields in DMA or ionic liquid [Bmim]BF4. This catalytic alternative of the Ullmann reaction has proved to be sensitive to both electronic and steric factors of substrates.
文摘Pyridine was used as a solvent for homocoupling of aryl bromides catalyzed by nickel chloride/triarylphosphine in the presence of zinc and recycled easily. Triphenylphosphine was the best ligand for nickel in this coupling reaction.
基金This work was supported by grants from the National Program on Key Research Project(No.2016YFA0602900)the National Natural Science Foundation of China(No.21871094)+2 种基金the Science and Technology Program of Guangzhou,China(No.201707010057)the Guangdong Natural Science Foundation(No.2017A030312005)the Science and Technology Planning Project of Guangdong Province,China(No.2017A020216021).
文摘Herein,we describe an environmentally benign and cost.efective protocol for the synthesis of valuable bifuranyl dicarboylates,starting with a-bromination of readily accessible furan-2-carboylates by LiBr and K_(2)S_(2)O_(8).Furthermore,the bromination intermediate product 5-bromofuran-2-carboxylates were then conducted in a palladium-catalyzed reductive homocoupling reactions in the pres-ence of alcohols to afford bifuranyl dicarboxylates.One of the final products in this protocol,[2,2']bifuran-5,5'-dicarboxylic acid es-ters,are essential monomers of poly(ethylene bifuranoate),which can be served as an green and versatile alternative polymer for traditional poly(ethylene terephthalate)that is currently common in technical plastics.
基金the National Natural Science Foundation of China(No.21572072)111 Project(No.BC2018061)and Y.Feng thanks the financial support of Scientific Research Foundation of Xiamen Huaxia University(No.HX201807)+1 种基金Outstanding Youth Scientific Research Cultivation Plan in Fujian Province University(No.201808)the Fujian Education and Scientific Research Project for Young and Middle-aged Teachers(No.JAT190990)。
文摘Pd-catalyzed oxidative homocoupling of 2-arylquinazolinones was successfully developed for the direct construction of biaryls via C—H bond activation.New well-defined structure that possessed two quinazolinone units was obtained with high efficiency and atomic economy.The protocols offer an efficient approach to the synthetically useful and functionalized biaryls in good yields using quinazolinone as a directing group.
基金the National Natural Science Foundation of China (No. 29972046) and Chinese Academy of Sciences.
文摘A new homocoupling methodology mediated by a novel combination of CuCl-2,2'-dipyridyl and its application to the synthesis of substituted polyfluorinated alka-2,4-dienes are described.
基金SERB,New Delhi,Grant/Award Number:CRG/2018/001274SERB Power fellowship,Grant/Award Number:SPF/2021/000019+2 种基金CSIR,New Delhi,Grant/Award Number:02(0358/19/EMR-II)RUSA2.0(Component-4)DST for support under FIST and PURSE programme。
文摘Photosensitizing supramolecular assemblies based on a phenazine derivative(PPA)have been developed,which show a strong affinity toward Pd2+ions to generate supramolecular ensemble PPA@Pd nanoparticles(NPs).The PPA@Pd NPs catalyse the Suzuki cross-coupled reaction under mild conditions(aerial conditions,mixed aqueous media,and visible light radiations).Although PPA@Pd NPs exhibit a strong affinity for arylboronic acid and could catalyse homocoupling of arylboronic acid,the preference of PPA assemblies for aryl halide directed the course of reactions toward the formation of cross-coupled products.The electron-rich PPA assemblies not only facilitate the oxidative addition step through photoinduced electron transfer to Pd^(2+)ions but also bring the reactants closer to the catalytic sites by selective interactions with aryl halides in the presence of arylboronic acid under visible light irradiation.The efficiency of PPA@Pd NPs to catalyse the Suzuki crosscoupled reaction has been demonstrated for the synthesis of unsymmetrically substituted terphenyl derivatives.
基金Project supported by the National Natural Science Foundation of China (No. 30873153), and the Key Projects of Shanghai in Biomedical (No. 08431902700).
文摘Symmetrical diynes were synthesized by ligand-free copper-catalyzed homocoupling reaction of 1,1-dibromo-1- alkenes using a DBU/DMSO system at room temperature in good to excellent yields.
基金Supported by the National Natural Science Foundation of China(Nos.51503037,51822308,51733004,21661132006)the Program for New Century Excellent Talents in Fujian Province Universities,China,the Fund of the Youth Innovation Promotion Association of the Chinese Academy of Sciences and the Education and Scientific Research Project for Young and Middle-aged Teachers in Fujian Province,China(No.JT180633).
文摘Copper/oxalic diamide-promoted dimerization of tetrachlorinated perylene bisimide to construct highly-fused diperylene bisimides through Ullmann coupling and zipper-mode double C—H activation has been developed in this study.This one-step reaction combining homocoupling with C—H activation proceeded smoothly under the action of inexpensive metal-ligand system.This protocol is expected to expand the available synthetic tools for condensed ring systems of perylene bisimide(PBIs).
文摘We present the mechanistic understanding of an electrochemically-driven nickel-catalyzed coupling reaction.Computational analysis reveals that the spin density is mostly residing on the nickel(Ni)center when Ni^(II) is reduced to NiI.Ni-mediated halogen atom abstraction through outer-sphere electron-transfer pathway to yield coupling products under mild conditions is demonstrated.Importantly,we have elucidated the role of Ni^(I) and Ni^(0) for successive coupling of benzyl bromide and benzyl chloride derivatives,respectively,to corresponding bibenzyl products.The Ni-catalyst bearing a PN^(3) P-ligand is an effective catalyst,producing a strong ligand effect on the reactivity and selectivity for the homocoupling reactions.