The optimizing utilization of ca rbon resources has drawn wide attention all over the world,while exploiting the high-efficiency catalytic routes remains a challenge.Here,a direct methanol synthesis route is realized ...The optimizing utilization of ca rbon resources has drawn wide attention all over the world,while exploiting the high-efficiency catalytic routes remains a challenge.Here,a direct methanol synthesis route is realized from pure CO and H_(2)O over 10%Cu/t-ZrO_(2) catalyst,where the time yield of methanol is144.43 mmol mol_(Cu)^(-1)h^(-1)and the methanol selectivity in hydrocarbons is 100%,The Cu species highly dispersed in the t-ZrO_(2) support lead parts of them in the cationic state.The Cu^(+)sites contribute to the dissociation of H_(2)O,providing the H*source for methanol synthesis,while the formed Cu^(0) sites promote the absorption and transfer of H*during the reaction.Moreover,the H_(2)O is even a better H resource than H_(2) due to its better dissociation effectivity in this catalytic system.The present work offers a new approach for methanol synthesis from CO and new insight into the process of supplying H donor.展开更多
β-Boryl amide is a class of high value intermediates in organic chemistry.In this work,a copper-catalyzed carbonylative boroamidation of olefins toward the synthesize ofβ-boryl amides has been developed.Several new ...β-Boryl amide is a class of high value intermediates in organic chemistry.In this work,a copper-catalyzed carbonylative boroamidation of olefins toward the synthesize ofβ-boryl amides has been developed.Several new chemical bonds were constructed in this transformation.A wide range ofβ-boryl amides were produced in excellent regioselectivity and good to excellent yields.Ethylene gas can be successfully transformed under the same standard conditions as well.Notably,with the use of a chiral ligand,the first example of enantioselective carbonylative boroamidation of alkenes was realized.In addition,Piposulfan and Pipobroman,antineoplastic medicines,were prepared by this methodology in a straightforward manner.展开更多
Functionalized bisboryl compounds have recently emerged as a new class of synthetically useful building blocks in organic synthesis.Herein,we report an efficient strategy to synthesizeβ-geminal-diboryl ketones enable...Functionalized bisboryl compounds have recently emerged as a new class of synthetically useful building blocks in organic synthesis.Herein,we report an efficient strategy to synthesizeβ-geminal-diboryl ketones enabled by a Cu/Pd-catalyzed borocarbonylative trifunctionalization of readily available alkynes and allenes.This reaction promises to be a useful method for the synthesis of functionalizedβ-geminal-diboryl ketones with broad functional group tolerance.Mechanistic studies suggest that the reaction proceeds through borocarbonylation/hydroboration cascade of both alkynes and allenes.展开更多
基金supported by the National Natural Science Foundation of China under grant numbers 22172032,U22A20431 and U19B2003。
文摘The optimizing utilization of ca rbon resources has drawn wide attention all over the world,while exploiting the high-efficiency catalytic routes remains a challenge.Here,a direct methanol synthesis route is realized from pure CO and H_(2)O over 10%Cu/t-ZrO_(2) catalyst,where the time yield of methanol is144.43 mmol mol_(Cu)^(-1)h^(-1)and the methanol selectivity in hydrocarbons is 100%,The Cu species highly dispersed in the t-ZrO_(2) support lead parts of them in the cationic state.The Cu^(+)sites contribute to the dissociation of H_(2)O,providing the H*source for methanol synthesis,while the formed Cu^(0) sites promote the absorption and transfer of H*during the reaction.Moreover,the H_(2)O is even a better H resource than H_(2) due to its better dissociation effectivity in this catalytic system.The present work offers a new approach for methanol synthesis from CO and new insight into the process of supplying H donor.
文摘β-Boryl amide is a class of high value intermediates in organic chemistry.In this work,a copper-catalyzed carbonylative boroamidation of olefins toward the synthesize ofβ-boryl amides has been developed.Several new chemical bonds were constructed in this transformation.A wide range ofβ-boryl amides were produced in excellent regioselectivity and good to excellent yields.Ethylene gas can be successfully transformed under the same standard conditions as well.Notably,with the use of a chiral ligand,the first example of enantioselective carbonylative boroamidation of alkenes was realized.In addition,Piposulfan and Pipobroman,antineoplastic medicines,were prepared by this methodology in a straightforward manner.
基金This work was supported by the Chinese Scholarship Council(CSC).
文摘Functionalized bisboryl compounds have recently emerged as a new class of synthetically useful building blocks in organic synthesis.Herein,we report an efficient strategy to synthesizeβ-geminal-diboryl ketones enabled by a Cu/Pd-catalyzed borocarbonylative trifunctionalization of readily available alkynes and allenes.This reaction promises to be a useful method for the synthesis of functionalizedβ-geminal-diboryl ketones with broad functional group tolerance.Mechanistic studies suggest that the reaction proceeds through borocarbonylation/hydroboration cascade of both alkynes and allenes.
