Trace amounts of palladium catalysed the Suzuki–Miyaura reaction of deactivated and hindered aryl chlorides-Reference-Cited by-同舟云学术

Trace amounts of palladium catalysed the Suzuki–Miyaura reaction of deactivated and hindered aryl chlorides

Published:2024 Issue:22 Volume:22 Page:4559-4567
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Li Zhenhua¹²^ORCID,Rong Dayou¹,Yuan Longfeng¹,Zhao Zhihong¹,Dai Fenghao¹,Chen Lijun¹,Xie Yuanyuan¹²^ORCID

Affiliation:

1. College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou, PR China

2. Key Laboratory for Green Pharmaceutical Technologies and Related Equipment of Ministry of Education, Key Laboratory of Pharmaceutical Engineering of Zhejiang Province, China

Abstract

A highly efficient catalytic system for the Suzuki–Miyaura reaction of deactivated and hindered aryl chlorides using trace amounts of commercial catalysts was reported.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D4OB00623B

Reference69 articles.

1. Pd Metal Catalysts for Cross-Couplings and Related Reactions in the 21st Century: A Critical Review

2. Big Data from Pharmaceutical Patents: A Computational Analysis of Medicinal Chemists’ Bread and Butter

3. Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst

4. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides

5. Carbon–carbon bonding made easy

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Practical method for the large-scale synthesis of 4′-chloro-2-nitrobiphenyl: A key intermediate of Boscalid;Advanced Agrochem;2024-09