A nickel-catalyzed Suzuki-Miyaura coupling reaction of aryl halides facilitated by pyridine derivatives-Reference-Cited by-同舟云学术

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A nickel-catalyzed Suzuki-Miyaura coupling reaction of aryl halides facilitated by pyridine derivatives

Published:2024-06 Issue: Volume:143 Page:155130
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Tan Jie,Gu Xuefeng,Dai Huiming,Song Yilian,Huang Zhibin,Zhao Yingsheng

Funder

Natural Science Research of Jiangsu Higher Education Institutions of China

Henan Normal University

Major Basic Research Project of the Natural Science Foundation of the Jiangsu Higher Education Institutions

NSFC

Publisher

Elsevier BV

Reference27 articles.

1. Large-scale applications of transition metal-catalyzed couplings for the synthesis of pharmaceuticals;Magano;Chem. Rev.,2011

2. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides;Miyaura;Tetrahedron Lett.,1979

3. The palladium-catalyzed cross-coupling reaction of phenylboronic acid with haloarenes in the presence of bases;Miyaura;Synth. Commun.,1981

4. Palladium-catalyzed cross-coupling reactions of organoboron compounds;Miyaura;Chem. Rev.,1995

5. Analysis of past and present synthetic methodologies on medicinal chemistry: where have all the new reactions gone?;Brown;J. Med. Chem.,2016

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