Fe(OTf)<sub>3</sub>-catalyzed annulation of α,β-unsaturated ketoxime acetates with enaminones for the synthesis of functionalized 2,4-diarylpyridines-Reference-Cited by-同舟云学术

Fe(OTf)₃-catalyzed annulation of α,β-unsaturated ketoxime acetates with enaminones for the synthesis of functionalized 2,4-diarylpyridines

Published:2023 Issue:17 Volume:10 Page:4298-4304
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Hu Xing-Mei¹,Yang Jing¹,Yang Jia-Ming¹,Shao Bi-Na¹,Huang Rong¹,Yan Sheng-Jiao¹^ORCID

Affiliation:

1. Key Laboratory of Medicinal Chemistry for Natural Resources, Ministry of Education, School of Chemical Science and Technology, Yunnan University, Kunming, 650091, P. R. China

Abstract

This method involves a cascade reaction utilizing 1 and enamines 2 as substrates, which occurred by refluxing a mixture of the starting materials in toluene with the catalyst Fe(OTf)3.

Funder

Applied Basic Research Foundation of Yunnan Province

Yunnan Provincial Department of Education

Yunnan University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/QO/D3QO00685A

Reference55 articles.

1. Discovery and SARs of 5-Chloro-N4-phenyl-N2-(pyridin-2-yl)pyrimidine-2,4-diamine Derivatives as Oral Available and Dual CDK 6 and 9 Inhibitors with Potent Antitumor Activity