Liu Yang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Liu Yang has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
- Chao Wang
Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi'an, 710062, China
2 shared publications - Dong Xue
Shaanxi Normal University
2 shared publications - Gang Li
Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education and School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi'an, 710062, China
2 shared publications - Jianliang Xiao
Department of Chemistry, University of Liverpool, Liverpool, UK
2 shared publications - Jian‐Jun Liu
Key Laboratory of Applied Surface and Colloid Chemistry Ministry of Education and School of Chemistry and Chemical Engineering Shaanxi Normal University Xi'an 710062 China
2 shared publications - Rui Cao
Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering Shaanxi Normal University Xi'an China
2 shared publications
Latest Publications
- 12 November 2020
- Published by Wiley in Angewandte Chemie
- Vol. 133 (10) , 5290-5294
Light‐Promoted C–N Coupling of Aryl Halides with Nitroarenes
A photochemical C–N coupling of aryl halides with nitroarenes is demonstrated for the first time. Catalyzed by a NiII complex in the absence of any external photosensitizer, readily available nitroarenes undergo coupling with a variety of aryl halides, providing a step‐economic extension to the widely used Buchwald–Hartwig C–N coupling reaction. The method tolerates coupling partners with steric‐congestion and functional groups sensitive to bases and nucleophiles. Mechanistic studies suggest that the reaction proceeds via the addition of an aryl radical, generated from a NiI/NiIII cycle, to a nitrosoarene intermediate.
- 12 November 2020
- Published by Wiley in Angewandte Chemie
- Vol. 133 (10) , 5290-5294
Light‐Promoted C–N Coupling of Aryl Halides with Nitroarenes
A photochemical C–N coupling of aryl halides with nitroarenes is demonstrated for the first time. Catalyzed by a NiII complex in the absence of any external photosensitizer, readily available nitroarenes undergo coupling with a variety of aryl halides, providing a step‐economic extension to the widely used Buchwald–Hartwig C–N coupling reaction. The method tolerates coupling partners with steric‐congestion and functional groups sensitive to bases and nucleophiles. Mechanistic studies suggest that the reaction proceeds via the addition of an aryl radical, generated from a NiI/NiIII cycle, to a nitrosoarene intermediate.
- 12 November 2020
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 60 (10) , 5230-5234
Light‐Promoted C–N Coupling of Aryl Halides with Nitroarenes
A photochemical C–N coupling of aryl halides with nitroarenes is demonstrated for the first time. Catalyzed by a NiII complex in the absence of any external photosensitizer, readily available nitroarenes undergo coupling with a variety of aryl halides, providing a step‐economic extension to the widely used Buchwald–Hartwig C–N coupling reaction. The method tolerates coupling partners with steric‐congestion and functional groups sensitive to bases and nucleophiles. Mechanistic studies suggest that the reaction proceeds via the addition of an aryl radical, generated from a NiI/NiIII cycle, to a nitrosoarene intermediate.
- 12 November 2020
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 60 (10) , 5230-5234
Light‐Promoted C–N Coupling of Aryl Halides with Nitroarenes
A photochemical C–N coupling of aryl halides with nitroarenes is demonstrated for the first time. Catalyzed by a NiII complex in the absence of any external photosensitizer, readily available nitroarenes undergo coupling with a variety of aryl halides, providing a step‐economic extension to the widely used Buchwald–Hartwig C–N coupling reaction. The method tolerates coupling partners with steric‐congestion and functional groups sensitive to bases and nucleophiles. Mechanistic studies suggest that the reaction proceeds via the addition of an aryl radical, generated from a NiI/NiIII cycle, to a nitrosoarene intermediate.