The artificial photosynthesis technology has been recognized as a promising solution for CO_(2) utilization.Photothermal catalysis has been proposed as a novel strategy to promote the efficiency of artificial photosyn...The artificial photosynthesis technology has been recognized as a promising solution for CO_(2) utilization.Photothermal catalysis has been proposed as a novel strategy to promote the efficiency of artificial photosynthesis by coupling both photochemistry and thermochemistry.However,strategies for maximizing the use of solar spectra with different frequencies in photothermal catalysis are urgently needed.Here,a hierarchical full-spectrum solar light utilization strategy is proposed.Based on this strategy,a Cu@hollow titanium silicalite-1 zeolite(TS-1)nanoreactor with spatially separated photo/thermal catalytic sites is designed to realize high-efficiency photothermal catalytic artificial photosynthesis.The space-time yield of alcohol products over the optimal catalyst reached 64.4μmol g−1 h−1,with the selectivity of CH3CH2OH of 69.5%.This rationally designed hierarchical utilization strategy for solar light can be summarized as follows:(1)high-energy ultraviolet light is utilized to drive the initial and difficult CO_(2) activation step on the TS-1 shell;(2)visible light can induce the localized surface plasmon resonance effect on plasmonic Cu to generate hot electrons for H2O dissociation and subsequent reaction steps;and(3)low-energy near-infrared light is converted into heat by the simulated greenhouse effect by cavities to accelerate the carrier dynamics.This work provides some scientific and experimental bases for research on novel,highly efficient photothermal catalysts for artificial photosynthesis.展开更多
The interaction between a promoter and an active metal crucially impacts catalytic performance.Nowadays,the influence of promoter contents and species has been intensively considered.In this study,we investigate the e...The interaction between a promoter and an active metal crucially impacts catalytic performance.Nowadays,the influence of promoter contents and species has been intensively considered.In this study,we investigate the effect of the iron(Fe)-zinc(Zn)proximity of Fe-Zn bimetallic catalysts on CO_(2)hydrogenation performance.To eliminate the size effect,Fe_(2)O_(3)and ZnO nanoparticles with uniform size are first prepared by the thermal decomposition method.By changing the loading sequence or mixing method,a series of Fe-Zn bimetallic catalysts with different Fe-Zn distances are obtained.Combined with a series of characterization techniques and catalytic performances,Fe-Zn bimetallic proximity for compositions of Fe species is discussed.Furthermore,we observe that a smaller Fe-Zn distance inhibits the reduction and carburization of the Fe species and facilitates the oxidation of carbides.Appropriate proximity of Fe and Zn(i.e.,Fe_1Zn_(1)-imp and Fe_(1)Zn_(1)-mix samples)results in a suitable ratio of the Fe_5C_(2)and Fe_(3)O_(4)phases,simultaneously promoting the reverse water-gas shift and Fischer-Tropsch synthesis reactions.This study provides insight into the proximity effect of bimetallic catalysts on CO_(2)hydrogenation performance.展开更多
Most of existed strategies for defending OFA (Objective Function Attack)are centralized, only suitable for small-scale networks and stressed on the computation complexity and traffic load are usually neglected. In thi...Most of existed strategies for defending OFA (Objective Function Attack)are centralized, only suitable for small-scale networks and stressed on the computation complexity and traffic load are usually neglected. In this paper, we pay more attentions on the OFA problem in large-scale cognitive networks, where the big data generated from the network must be considered and the traditional methods could be of helplessness. In this paper, we first analyze the interactive processes between attacker and defender in detail, and then a defense strategy for OFA based on differential game is proposed, abbreviated as DSDG. Secondly, the game saddle point and optimal defense strategy have proved to be existed simultaneously. Simulation results show that the proposed DSDG has a less influence on network performance and a lower rate of packet loss.More importantly, it can cope with the large range展开更多
Tocopherol is an important lipid-soluble antioxidant beneficial for both human health and plant growth. Here, we fine mapped a major QTLqVE1 affecting γ-tocopherol content in maize kernel, positionally cloned and con...Tocopherol is an important lipid-soluble antioxidant beneficial for both human health and plant growth. Here, we fine mapped a major QTLqVE1 affecting γ-tocopherol content in maize kernel, positionally cloned and confirmed the underlying gene ZmPORB1(por1), as a protochlorophyllide oxidoreductase. A 13.7 kb insertion reduced the tocopherol and chlorophyll content, and the photosynthetic activity by repressing ZmPORB1 expression in embryos of NIL-K22, but did not affect the levels of the tocopherol precursors HGA(homogentisic acid)and PMP(phytyl monophosphate). Furthermore, ZmPORB1 is inducible by low oxygen and light, thereby involved in the hypoxia response in developing embryos. Concurrent with natural hypoxia in embryos, the redox state has been changed with NO increasing and H_(2)O_(2) decreasing, which lowered γ-tocopherol content via scavenging reactive nitrogen species. In conclusion, we proposed that the lower lightharvesting chlorophyll content weakened embryo photosynthesis, leading to fewer oxygen supplies and consequently diverse hypoxic responses including an elevated γ-tocopherol consumption. Our findings shed light on the mechanism for fine-tuning endogenous oxygen concentration in the maize embryo through a novel feedback pathway involving the light and low oxygen regulation of ZmPORB1 expression and chlorophyll content.展开更多
Plant natural products have been extensively exploited in food,medicine,flavor,cosmetic,renewable fuel,and other industrial sectors.Synthetic biology has recently emerged as a promising means for the cost-effective an...Plant natural products have been extensively exploited in food,medicine,flavor,cosmetic,renewable fuel,and other industrial sectors.Synthetic biology has recently emerged as a promising means for the cost-effective and sustainable production of natural products.Compared with engineering microbes for the production of plant natural products,the potential of plants as chassis for producing these compounds is underestimated,largely due to challenges encountered in engineering plants.Knowledge in plant engineering is instrumental for enabling the effective and efficient production of valuable phytochemicals in plants,and also paves the way for a more sustainable future agriculture.In this manuscript,we briefly recap the biosynthesis of plant natural products,focusing primarily on industrially important terpenoids,alkaloids,and phenylpropanoids.We further summarize the plant hosts and strategies that have been used to engineer the production of natural products.The challenges and opportunities of using plant synthetic biology to achieve rapid and scalable production of high-value plant natural products are also discussed.展开更多
The phytohormone salicylic acid(SA)regulates biotic and abiotic stress responses in plants.Two distinct biosynthetic pathways for SA have been well documented in plants:the isochorismate(IC)pathway in the chloroplast ...The phytohormone salicylic acid(SA)regulates biotic and abiotic stress responses in plants.Two distinct biosynthetic pathways for SA have been well documented in plants:the isochorismate(IC)pathway in the chloroplast and the phenylalanine ammonia-lyase(PAL)pathway in the cytosol.However,there has been no solid evidence that the PAL pathway contributes to SA biosynthesis.Here,we report that feeding Arabidopsis thaliana with Ring-13C-labeled phenylalanine(13C6-Phe)resulted in incorporation of the13C label not into SA,but into its isomer 4-hydroxybenzoic acid(4-HBA)instead.We obtained similar results when feeding13C6-Phe to the SA-deficient ics1 ics2 mutant and the SA-hyperaccumulating mutant s3h s5h.Notably,we detected13C6-SA when13C6-benzoic acid(BA)was provided,suggesting that SA can be synthesized from BA.Furthermore,despite the substantial accumulation of SA upon pathogen infection,we did not observe incorporation of13C label from Phe into SA.We also did not detect13C6-SA in PAL-overexpressing lines in the kfb01 kfb02 kfb39 kfb50 background after being fed13C6-Phe,although endogenous PAL levels were dramatically increased.Based on these combined results,we propose that SA biosynthesis is not from Phe in Arabidopsis.These results have important implications for our understanding of the SA biosynthetic pathway in land plants.展开更多
The conversion from syngas derived from non-petroleum recourses to liquid fuels and chemicals via Fischer–Tropsch synthesis(FTS)is regarded as an alternative and potential route.Developing catalyst with controllable ...The conversion from syngas derived from non-petroleum recourses to liquid fuels and chemicals via Fischer–Tropsch synthesis(FTS)is regarded as an alternative and potential route.Developing catalyst with controllable particle size and clarifying size effect are of significance to promote the process.Herein,we engineered carbon-encapsulation structure to restrict particle growth but avoid strong metal–support interactions.The prepared carbon-encapsulated nanoparticles(Fe@C)showed a superior catalytic activity compared with conventional carbon-supported nanoparticles(Fe/C).By tuning particle size from 3.0 to 9.1 nm,a volcano-like trend of iron time yield(FTY)peaked at 2659μmol·gFe^(−1)·s^(−1)is obtained with an optimum particle size of 5.3 nm.According to temperature-programmed reduction and desorption results,a linear relationship between apparent turnover frequency and CO dissociation capacity was established.The enhanced CO dissociative adsorption along with weakened H_(2)activation on larger nanoparticles resulted in higher C_(5+)selectivity.This study provides a strategy to synthesize carbon supported metal catalysts with controllable particle size and insight into size effect on Fe-based catalytic FTS.展开更多
The Fischer--Tropsch synthesis(FTS)con-tinues to be an attractive alternative for producing a broad range of fuels and chemicals through the conversion of syngas(H2 and CO),which can be derived from various sources,su...The Fischer--Tropsch synthesis(FTS)con-tinues to be an attractive alternative for producing a broad range of fuels and chemicals through the conversion of syngas(H2 and CO),which can be derived from various sources,such as coal,natural gas,and biomass.Among iron carbides,Fe2C,as an active phase,has barely been studied due to its thermodynamic instability.Here,we fabricated a series of Fe2C embedded in hollow carbon sphere(HCS)catalysts.By varying the crystallization time,the shell thickness of the HCS was manipulated,which significantly influenced the catalytic performance in the FTS.To investigate the relationship between the geometric structure of the HCS and the physic-chemical properties of Fe species,transmission electron microscopy,X-ray diffraction,N2 physical adsorption,X-ray photo-electron spectroscopy,hydrogen temperature-programmed reduction,Raman spectroscopy,and Mossbauer spectro-scopy techniques were employed to characterize the catalysts before and after the reaction.Evidently,a suitable thickness of the carbon layer was beneficial for enhancing the catalytic activity in the FTS due to its high porosity,appropriate electronic environment,and relatively high Fe2C content.展开更多
Glycosylation by uridine diphosphate-dependent glycosyltransferases(UGTs)in plants contributes to the complexity and diversity of secondary metabolites.UGTs are generally promiscuous in their use of acceptors,making i...Glycosylation by uridine diphosphate-dependent glycosyltransferases(UGTs)in plants contributes to the complexity and diversity of secondary metabolites.UGTs are generally promiscuous in their use of acceptors,making it challenging to reveal the function of UGTs in vivo.Here,we described an approach that combined glycoside-specific metabolomics and precursor isotopic labeling analysis to characterize UGTs in Arabidopsis.We revisited the UGT72E cluster,which has been reported to catalyze the glycosylation of monolignols.Glycoside-specific metabolomics analysis reduced the number of differentially accumulated metabolites in the ugt72e1e2e3 mutant by at least 90%compared with that from traditional untargeted metabolomics analysis.In addition to the two previously reported monolignol glycosides,a total of 62 glycosides showed reduced accumulation in the ugt72e1e2e3 mutant,22 of which were phenylalanine-derived glycosides,including 5-OH coniferyl alcohol-derived and lignan-derived glycosides,as confirmed by isotopic tracing of[^(13)C_(6)]-phenylalanine precursor.Our method revealed that UGT72Es could use coumarins as substrates,and genetic evidence showed that UGT72Es endowed plants with enhanced tolerance to low iron availability under alkaline conditions.Using the newly developed method,the function of UGT78D2 was also evaluated.These case studies suggest that this method can substantially contribute to the characterization of UGTs and efficiently investigate glycosylation processes,the complexity of which have been highly underestimated.展开更多
The Pd-catalyzed homodimerization with respect to arylsulfonyl chlorides as an efficient method for the synthesisof biaryls has been developed. This desulfonylative reaction which was performed at reflux in 1,4-dioxan...The Pd-catalyzed homodimerization with respect to arylsulfonyl chlorides as an efficient method for the synthesisof biaryls has been developed. This desulfonylative reaction which was performed at reflux in 1,4-dioxane for 4h under air afforded the desired products in good to excellent yields.展开更多
基金supported by the National Natural Science Foundation of China(Grant Nos.21908052 and 22108200)the Key Program of the Natural Science Foundation of Hebei Province(Grant No.B2020209017)+2 种基金the Project of Science and Technology Innovation Team,Tangshan(Grant No.20130203D)the Natural Science Foundation of Zhejiang Province(Grant No.LQ22B060013)and the Science and Technology Project of Hebei Education Department(Grant No.QN2021113).
文摘The artificial photosynthesis technology has been recognized as a promising solution for CO_(2) utilization.Photothermal catalysis has been proposed as a novel strategy to promote the efficiency of artificial photosynthesis by coupling both photochemistry and thermochemistry.However,strategies for maximizing the use of solar spectra with different frequencies in photothermal catalysis are urgently needed.Here,a hierarchical full-spectrum solar light utilization strategy is proposed.Based on this strategy,a Cu@hollow titanium silicalite-1 zeolite(TS-1)nanoreactor with spatially separated photo/thermal catalytic sites is designed to realize high-efficiency photothermal catalytic artificial photosynthesis.The space-time yield of alcohol products over the optimal catalyst reached 64.4μmol g−1 h−1,with the selectivity of CH3CH2OH of 69.5%.This rationally designed hierarchical utilization strategy for solar light can be summarized as follows:(1)high-energy ultraviolet light is utilized to drive the initial and difficult CO_(2) activation step on the TS-1 shell;(2)visible light can induce the localized surface plasmon resonance effect on plasmonic Cu to generate hot electrons for H2O dissociation and subsequent reaction steps;and(3)low-energy near-infrared light is converted into heat by the simulated greenhouse effect by cavities to accelerate the carrier dynamics.This work provides some scientific and experimental bases for research on novel,highly efficient photothermal catalysts for artificial photosynthesis.
基金supported by National Natural Science Foundation of China(Nos.22108200,21938008 and 22121004)Natural Science Foundation of Zhejiang Province(LQ22B060013)the Haihe Laboratory of Sustainable Chemical Transformations for financial support。
文摘The interaction between a promoter and an active metal crucially impacts catalytic performance.Nowadays,the influence of promoter contents and species has been intensively considered.In this study,we investigate the effect of the iron(Fe)-zinc(Zn)proximity of Fe-Zn bimetallic catalysts on CO_(2)hydrogenation performance.To eliminate the size effect,Fe_(2)O_(3)and ZnO nanoparticles with uniform size are first prepared by the thermal decomposition method.By changing the loading sequence or mixing method,a series of Fe-Zn bimetallic catalysts with different Fe-Zn distances are obtained.Combined with a series of characterization techniques and catalytic performances,Fe-Zn bimetallic proximity for compositions of Fe species is discussed.Furthermore,we observe that a smaller Fe-Zn distance inhibits the reduction and carburization of the Fe species and facilitates the oxidation of carbides.Appropriate proximity of Fe and Zn(i.e.,Fe_1Zn_(1)-imp and Fe_(1)Zn_(1)-mix samples)results in a suitable ratio of the Fe_5C_(2)and Fe_(3)O_(4)phases,simultaneously promoting the reverse water-gas shift and Fischer-Tropsch synthesis reactions.This study provides insight into the proximity effect of bimetallic catalysts on CO_(2)hydrogenation performance.
基金This work is supported by the Research Fund for the Doctoral Program of Higher Education of China (20122304130002), the Natural Science Foundation of China (61370212), the Natural Science Foundation of Heilongjiang Province (ZD 201102), the Fundamental Research Fund for the Central Universities (HEUCFZ1213, HEUCF100601), and Postdoctoral Science Foundation of Heilongjiang Province (LBH-210204).
文摘Most of existed strategies for defending OFA (Objective Function Attack)are centralized, only suitable for small-scale networks and stressed on the computation complexity and traffic load are usually neglected. In this paper, we pay more attentions on the OFA problem in large-scale cognitive networks, where the big data generated from the network must be considered and the traditional methods could be of helplessness. In this paper, we first analyze the interactive processes between attacker and defender in detail, and then a defense strategy for OFA based on differential game is proposed, abbreviated as DSDG. Secondly, the game saddle point and optimal defense strategy have proved to be existed simultaneously. Simulation results show that the proposed DSDG has a less influence on network performance and a lower rate of packet loss.More importantly, it can cope with the large range
基金supported by the National Natural Science Foundation of China(32200221,U1901201)the National Key Research and Development Program of China(2022YFD1201502)+1 种基金the Key Area Research and Development Program of Guangdong Province,China(2022B0202060003)Huazhong Agricultural University Scientific&Technological Self-Innovation Foundation。
文摘Tocopherol is an important lipid-soluble antioxidant beneficial for both human health and plant growth. Here, we fine mapped a major QTLqVE1 affecting γ-tocopherol content in maize kernel, positionally cloned and confirmed the underlying gene ZmPORB1(por1), as a protochlorophyllide oxidoreductase. A 13.7 kb insertion reduced the tocopherol and chlorophyll content, and the photosynthetic activity by repressing ZmPORB1 expression in embryos of NIL-K22, but did not affect the levels of the tocopherol precursors HGA(homogentisic acid)and PMP(phytyl monophosphate). Furthermore, ZmPORB1 is inducible by low oxygen and light, thereby involved in the hypoxia response in developing embryos. Concurrent with natural hypoxia in embryos, the redox state has been changed with NO increasing and H_(2)O_(2) decreasing, which lowered γ-tocopherol content via scavenging reactive nitrogen species. In conclusion, we proposed that the lower lightharvesting chlorophyll content weakened embryo photosynthesis, leading to fewer oxygen supplies and consequently diverse hypoxic responses including an elevated γ-tocopherol consumption. Our findings shed light on the mechanism for fine-tuning endogenous oxygen concentration in the maize embryo through a novel feedback pathway involving the light and low oxygen regulation of ZmPORB1 expression and chlorophyll content.
基金supported by the National Natural Science Foundation of China(Grant No.32061143023)Shenzhen Municipal Startup Fund and the Key Laboratory of Molecular Design for Plant Cell Factory of Guangdong Higher Education Institutes(Grant No.2019KSYS006)。
文摘Plant natural products have been extensively exploited in food,medicine,flavor,cosmetic,renewable fuel,and other industrial sectors.Synthetic biology has recently emerged as a promising means for the cost-effective and sustainable production of natural products.Compared with engineering microbes for the production of plant natural products,the potential of plants as chassis for producing these compounds is underestimated,largely due to challenges encountered in engineering plants.Knowledge in plant engineering is instrumental for enabling the effective and efficient production of valuable phytochemicals in plants,and also paves the way for a more sustainable future agriculture.In this manuscript,we briefly recap the biosynthesis of plant natural products,focusing primarily on industrially important terpenoids,alkaloids,and phenylpropanoids.We further summarize the plant hosts and strategies that have been used to engineer the production of natural products.The challenges and opportunities of using plant synthetic biology to achieve rapid and scalable production of high-value plant natural products are also discussed.
基金supported by the National Key Research and Development Program of China(2021YFD2201000,2019YFA0903900)National Natural Science Foundation of China(31870273)+1 种基金Shenzhen Key Laboratory of Synthetic Genomics(ZDSYS201802061806209)The Strategic Priority Research Program of the Chinese Academy of Sciences(XDPB18)。
文摘The phytohormone salicylic acid(SA)regulates biotic and abiotic stress responses in plants.Two distinct biosynthetic pathways for SA have been well documented in plants:the isochorismate(IC)pathway in the chloroplast and the phenylalanine ammonia-lyase(PAL)pathway in the cytosol.However,there has been no solid evidence that the PAL pathway contributes to SA biosynthesis.Here,we report that feeding Arabidopsis thaliana with Ring-13C-labeled phenylalanine(13C6-Phe)resulted in incorporation of the13C label not into SA,but into its isomer 4-hydroxybenzoic acid(4-HBA)instead.We obtained similar results when feeding13C6-Phe to the SA-deficient ics1 ics2 mutant and the SA-hyperaccumulating mutant s3h s5h.Notably,we detected13C6-SA when13C6-benzoic acid(BA)was provided,suggesting that SA can be synthesized from BA.Furthermore,despite the substantial accumulation of SA upon pathogen infection,we did not observe incorporation of13C label from Phe into SA.We also did not detect13C6-SA in PAL-overexpressing lines in the kfb01 kfb02 kfb39 kfb50 background after being fed13C6-Phe,although endogenous PAL levels were dramatically increased.Based on these combined results,we propose that SA biosynthesis is not from Phe in Arabidopsis.These results have important implications for our understanding of the SA biosynthetic pathway in land plants.
基金the National Natural Science Foundation of China(No.U20A20124)the Program of Introducing Talents of Discipline to Universities(No.BP0618007)are gratefully acknowledged.
文摘The conversion from syngas derived from non-petroleum recourses to liquid fuels and chemicals via Fischer–Tropsch synthesis(FTS)is regarded as an alternative and potential route.Developing catalyst with controllable particle size and clarifying size effect are of significance to promote the process.Herein,we engineered carbon-encapsulation structure to restrict particle growth but avoid strong metal–support interactions.The prepared carbon-encapsulated nanoparticles(Fe@C)showed a superior catalytic activity compared with conventional carbon-supported nanoparticles(Fe/C).By tuning particle size from 3.0 to 9.1 nm,a volcano-like trend of iron time yield(FTY)peaked at 2659μmol·gFe^(−1)·s^(−1)is obtained with an optimum particle size of 5.3 nm.According to temperature-programmed reduction and desorption results,a linear relationship between apparent turnover frequency and CO dissociation capacity was established.The enhanced CO dissociative adsorption along with weakened H_(2)activation on larger nanoparticles resulted in higher C_(5+)selectivity.This study provides a strategy to synthesize carbon supported metal catalysts with controllable particle size and insight into size effect on Fe-based catalytic FTS.
基金Financial support from the National Natural Science Foundation of China(Grant No.U1462204)Natural Science Foundation of Tianjin City(No.8JCQNJC05900)is grateflilly acknowledged.
文摘The Fischer--Tropsch synthesis(FTS)con-tinues to be an attractive alternative for producing a broad range of fuels and chemicals through the conversion of syngas(H2 and CO),which can be derived from various sources,such as coal,natural gas,and biomass.Among iron carbides,Fe2C,as an active phase,has barely been studied due to its thermodynamic instability.Here,we fabricated a series of Fe2C embedded in hollow carbon sphere(HCS)catalysts.By varying the crystallization time,the shell thickness of the HCS was manipulated,which significantly influenced the catalytic performance in the FTS.To investigate the relationship between the geometric structure of the HCS and the physic-chemical properties of Fe species,transmission electron microscopy,X-ray diffraction,N2 physical adsorption,X-ray photo-electron spectroscopy,hydrogen temperature-programmed reduction,Raman spectroscopy,and Mossbauer spectro-scopy techniques were employed to characterize the catalysts before and after the reaction.Evidently,a suitable thickness of the carbon layer was beneficial for enhancing the catalytic activity in the FTS due to its high porosity,appropriate electronic environment,and relatively high Fe2C content.
基金the National Key R&D Program of China(2019YFA0903900)National Natural Science Foundation of China(grant number 31870273)+2 种基金Guangdong Provincial Key Laboratory of Synthetic Genomics(2019B030301006)Shenzhen Key Laboratory of Synthetic Genomics(ZDSYS201802061806209)Shenzhen Instituteof Synthetic Biology Scientific Research Program(ZTXM20190007).
文摘Glycosylation by uridine diphosphate-dependent glycosyltransferases(UGTs)in plants contributes to the complexity and diversity of secondary metabolites.UGTs are generally promiscuous in their use of acceptors,making it challenging to reveal the function of UGTs in vivo.Here,we described an approach that combined glycoside-specific metabolomics and precursor isotopic labeling analysis to characterize UGTs in Arabidopsis.We revisited the UGT72E cluster,which has been reported to catalyze the glycosylation of monolignols.Glycoside-specific metabolomics analysis reduced the number of differentially accumulated metabolites in the ugt72e1e2e3 mutant by at least 90%compared with that from traditional untargeted metabolomics analysis.In addition to the two previously reported monolignol glycosides,a total of 62 glycosides showed reduced accumulation in the ugt72e1e2e3 mutant,22 of which were phenylalanine-derived glycosides,including 5-OH coniferyl alcohol-derived and lignan-derived glycosides,as confirmed by isotopic tracing of[^(13)C_(6)]-phenylalanine precursor.Our method revealed that UGT72Es could use coumarins as substrates,and genetic evidence showed that UGT72Es endowed plants with enhanced tolerance to low iron availability under alkaline conditions.Using the newly developed method,the function of UGT78D2 was also evaluated.These case studies suggest that this method can substantially contribute to the characterization of UGTs and efficiently investigate glycosylation processes,the complexity of which have been highly underestimated.
基金the National Natural Science Foundation of China(Nos.21272069,20672035)the Fundamental Research Funds for the Central Universities,and the Key Laboratory of Organofluorine Chemistry,Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences.
文摘The Pd-catalyzed homodimerization with respect to arylsulfonyl chlorides as an efficient method for the synthesisof biaryls has been developed. This desulfonylative reaction which was performed at reflux in 1,4-dioxane for 4h under air afforded the desired products in good to excellent yields.