Zhongqi Shao

Taiyuan University of Technology

Author Statistics

Papers

Citation

H-Index

i-10 index

Research Trends

Author Order

Document Type

Co-Authors

Wenlong Wei

Jiangsu Police Officer College

Xing Li

Taiyuan University of Technology

Honghong Chang

Taiyuan University of Technology

Wen‐Chao Gao

Taiyuan University of Technology

Tingting Zhu

Southeast University

Yingjun Li

Southwest University of Science and Technology

Yongli Zhang

Yale University

Wenwen Chen

Shanghai Normal University

Honghong Chang

Taiyuan University of Technology

Cooperative Institutions

Taiyuan University of Technology

Shanxi Zhendong Pharmaceutical (China)

State Council of the People's Republic of China

Institute of Coal Chemistry

East China Normal University

Tohoku University

Nanyang Normal University

Green Chemistry

Tianjin University

Zhengzhou University

Author Statistics

Papers

Citation

H-Index

i-10 index

Research Field

Newly-generated Al(OH) 3 -supported Pd nanoparticles-catalyzed Stille and Kumada coupling reactions of diazonium salts, (Het)aryl chlorides

Tetrahedron (2015)

Xing Li Tingting Zhu Zhongqi Shao Yingjun Li Honghong Chang

Stille reaction

Tetrafluoroborate

Coupling reaction

10.1016/j.tet.2015.10.069

Cite

Citations (22)

An Efficient Pd/Al(OH)3 Nanoparticle Catalyst for Suzuki Coupling Reactions of Aryl Halides

Synthesis (2014)

Xing Li Wenlong Wei Wenwen Chen Honghong Chang Zhongqi Shao

A high-performance palladium-based Pd/Al(OH)₃ catalyst has been prepared by the one-pot three-component method. It was found that this 'ligandless' Pd/Al(OH)₃ catalyst showed remarkable reactivity and gave excellent yields (up to 99%) towards the condensation of aryl bromides with various arylboronic acids under mild conditions, and afforded good yields of the coupling products (up to 97%) with most aryl chlorides in two different catalytic systems. Furthermore, this catalyst could be easily recovered through filtration and reused for 8 cycles without significant loss of the yield.

Filtration (mathematics)

Reactivity

Coupling reaction

Suzuki reaction

10.1055/s-0033-1341084

Cite

Citations (9)

ChemInform Abstract: An Efficient Pd/Al(OH)₃ Nanoparticle Catalyst for Suzuki Coupling Reactions of Aryl Halides.

ChemInform (2014)

Xing Li Wenwen Chen Honghong Chang Zhongqi Shao Wenlong Wei

Abstract The title catalyst shows high activity and gives excellent yields towards the condensation of aryl bromides with arlyboronic acids.

Coupling reaction

10.1002/chin.201450085

Cite

Citations (0)

ChemInform Abstract: Newly-Generated Al(OH)₃-Supported Pd Nanoparticles-Catalyzed Stille and Kumada Coupling Reactions of Diazonium Salts, (Het)aryl Chlorides.

ChemInform (2016)

Xing Li Tingting Zhu Zhongqi Shao Yingjun Li Honghong Chang

The title reaction features excellent functional group compatibility, moderate to good yields, and feasibility of using heteroaryl chlorides, diazonium salts, and Grignard reagents.

Stille reaction

Coupling reaction

Functional group

10.1002/chin.201620094

Cite

Citations (0)