Highly active palladium catalysts containing a 1,10-phenanthroline analogue N-heterocyclic carbene for room temperature Suzuki-Miyaura coupling reactions of aryl chlorides with arylboronic acids in aqueous media-Reference-Cited by-同舟云学术

Highly active palladium catalysts containing a 1,10-phenanthroline analogue N-heterocyclic carbene for room temperature Suzuki-Miyaura coupling reactions of aryl chlorides with arylboronic acids in aqueous media

Published:2017-02 Issue:8 Volume:58 Page:726-731
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Liu Guiyan,Liu Chengxin,Han Fangwai,Wang Zhongliang,Wang Jianhui

Funder

National Natural Science Foundation of China

Natural Science Foundation of Tianjin

Innovation Team Plan of the Tianjin Education Committee

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference67 articles.

1. The Synthesis of OSU 6162: Efficient, Large-Scale Implementation of a Suzuki Coupling

2. A General Method for the Suzuki−Miyaura Cross-Coupling of Sterically Hindered Aryl Chlorides: Synthesis of Di- and Tri-ortho-substituted Biaryls in 2-Propanol at Room Temperature

3. Effiziente Katalysatorsysteme für die Suzuki-Miyaura-Kupplung durch rationales Ligandendesign

4. Practical synthesis of new and highly efficient ligands for the Suzuki reaction of aryl chlorides

5. Catalytic Suzuki Coupling Reactions by Amido Phosphine Complexes of Palladium

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