Facile synthesis of pyrazolopyridine pharmaceuticals under mild conditions using an algin-functionalized silica-based magnetic nanocatalyst (Alg@SBA-15/Fe<sub>3</sub>O<sub>4</sub>)-Reference-Cited by-同舟云学术

Facile synthesis of pyrazolopyridine pharmaceuticals under mild conditions using an algin-functionalized silica-based magnetic nanocatalyst (Alg@SBA-15/Fe₃O₄)

Published:2023 Issue:15 Volume:13 Page:10367-10378
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Hassanzadeh-Afruzi Fereshte¹^ORCID,Amiri-Khamakani Zeinab¹,Saeidirad Mahdi¹,Salehi Mohammad Mehdi¹,Taheri-Ledari Reza¹^ORCID,Maleki Ali¹^ORCID

Affiliation:

1. Catalysts and Organic Synthesis Research Laboratory, Department of Chemistry, Iran University of Science and Technology, Tehran 16846-13114, Iran

Abstract

Pyrazolopyridines are common scaffolds in various bioactive compounds, which have several therapeutic effects and unique pharmacological properties.

Funder

Iran University of Science and Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/RA/D2RA07228A

Reference58 articles.

1. Synthesis of pyrazolopyridine and pyrazoloquinoline derivatives by one-pot, three-component reactions of arylglyoxals, 3-methyl-1-aryl-1H-pyrazol-5-amines and cyclic 1,3-dicarbonyl compounds in the presence of tetrapropylammonium bromide

2. Tetrahydrocarbazole amides with potent activity against human papillomaviruses

3. Antileishmanial Pyrazolopyridine Derivatives: Synthesis and Structure−Activity Relationship Analysis

4. Antimalarials. 4-Substituted 1H-pyrazolo[3,4-b]quinolines

5. Efficient synthesis of pyrazolopyridines containing a chromane backbone through domino reaction

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