Synthesis of indazoles from 2-formylphenylboronic acids
Author:
Affiliation:
1. Latvian Institute of Organic Synthesis
2. Riga
3. Latvia
4. Faculty of Materials Science and Applied Chemistry
5. Riga Technical University
Abstract
A method for the synthesis of indazoles was developed which involves a copper(ii) acetate catalysed reaction of 2-formylboronic acids with diazadicaboxylates followed by acid or base induced ring closure.
Funder
H2020 Marie Skłodowska-Curie Actions
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2021/RA/D1RA04056A
Reference21 articles.
1. Development of Dihydropyridone Indazole Amides as Selective Rho-Kinase Inhibitors
2. Discovery of indazoles as inhibitors of Tpl2 kinase
3. Probing 2 H ‐Indazoles as Templates for SGK1, Tie2, and SRC Kinase Inhibitors
4. Recent Advances in Indazole-Containing Derivatives: Synthesis and Biological Perspectives
5. Efficient Synthesis of 5-(Bromomethyl)- and 5-(Aminomethyl)-1-THP-Indazole
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