2024/5/6 -We disclose a highly efficient thermal Ni-catalyzed C–O cross-coupling of aryl halides with primary and secondary alcohols, without the need for photo- or ...
2023/11/16 -It provides an attractive alternative for the selective installation of a functional group at remote C–H positions from simple precursors, thus enabling the ...
2023/11/30 -Conspectus. Nickel excels at facilitating selective radical chemistry, playing a pivotal role in metalloenzyme catalysis and modern cross-coupling reactions.
2024/9/3 -This method allows for the synthesis of axially chiral biaryls from readily available coupling partners, such as aldehydes, ethers, and unactivated alkyl ...
2023/11/1 -A general method for the Ni-catalyzed Buchwald–Hartwig amination of (hetero)aryl chlorides using both anilines and aliphatic amines under homogeneous ...
2023/11/30 -Nickel excels at facilitating selective radical chemistry, playing a pivotal role in metalloenzyme catalysis and modern cross-coupling reactions. Radicals, ...
2024/9/10 -We established a highly efficient deoxygenative cross-coupling reaction using alcohols and industrial preferred aryl chlorides as coupling partners.
2024/2/12 -ACS Catal. 2019, 9, 6751–6754. (3) We reported the first Ni-catalyzed enantioselective reductive cross-coupling driven by electrochemistry.
2023/11/7 -The coupling reaction initiates with halogen atom abstraction at the secondary alkyl iodide. The alkyl Ni(II) complex then proceeds through a stereospecific SN2 ...
2023/11/30 -Nickel excels at facilitating selective radical chemistry, playing a pivotal role in metalloenzyme catalysis and modern cross-coupling reactions.