Efficient symmetrical bidentate dioxime ligand-accelerated homogeneous palladium-catalyzed Suzuki–Miyaura coupling reactions of aryl chlorides-Reference-Cited by-同舟云学术

Efficient symmetrical bidentate dioxime ligand-accelerated homogeneous palladium-catalyzed Suzuki–Miyaura coupling reactions of aryl chlorides

Published:2017 Issue:1 Volume:41 Page:372-376
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Song Jinyi¹²³⁴⁵,Zhao Hongyan¹²³⁴⁵,Liu Yang¹²³⁴⁵,Han Huatao¹²³⁴⁵,Li Zhuofei¹²³⁴⁵,Chu Wenyi¹²³⁴⁵,Sun Zhizhong¹²³⁴⁵

Affiliation:

1. School of Chemistry and Materials Science

2. Heilongjiang University

3. Harbin 150080

4. P. R. China

5. Key Laboratory of Chemical Engineering Process & Technology for High-efficiency Conversion

Abstract

A series of N,O-bidentate ligands were synthesized and studied as high activity ligands for palladium-catalyzed Suzuki–Miyaura cross-coupling reactions of aryl chlorides with arylboronic acids under mild conditions.

Funder

Natural Science Foundation of Heilongjiang Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2017/NJ/C6NJ02815B

Reference32 articles.

1. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds

2. Transition Metal-Catalyzed Activation of Aliphatic C−X Bonds in Carbon−Carbon Bond Formation

3. Cross-Coupling Reactions Of Organoboranes: An Easy Way To Construct CC Bonds (Nobel Lecture)

4. The B-Alkyl Suzuki-Miyaura Cross-Coupling Reaction: Development, Mechanistic Study, and Applications in Natural Product Synthesis

5. A highly active and reusable heterogeneous catalyst for the Suzuki reaction: synthesis of biaryls and polyaryls

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