Oxidative sulfonamidomethylation of imidazopyridines utilizing methanol as the main C1 source-Reference-Cited by-同舟云学术

Oxidative sulfonamidomethylation of imidazopyridines utilizing methanol as the main C1 source

Published:2019 Issue:19 Volume:17 Page:4869-4878
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Zhao Xue-Mei¹²³⁴⁵,Huang En-Ling¹²³⁴⁵,Zhu Yu-Shen¹²³⁴⁵,Li Jing¹²³⁴⁵,Song Bing¹²³⁴⁵,Zhu Xinju¹²³⁴⁵^ORCID,Hao Xin-Qi¹²³⁴⁵

Affiliation:

1. College of Chemistry and Molecular Engineering

2. School of Life Sciences

3. Zhengzhou University

4. Zhengzhou 450001

5. People's Republic of China

Abstract

An efficient one pot, three component synthesis of C3 sulfonamidomethylated imidazopyridines has been disclosed utilizing methanol and DTBP as the major and minor methylene source, respectively.

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Natural Science Foundation of Henan Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C9OB00596J

Reference81 articles.

1. Recent Progress in the Pharmacology of Imidazo[1,2-a]pyridines

2. Imidazopyridines as a source of biological activity and their pharmacological potentials—Infrared and Raman spectroscopic evidence of their content in pharmaceuticals and plant materials

3. Imidazo[1,2-a]pyridines: Promising Drug Candidate for Antitumor Therapy

4. Medicinal Attributes of Imidazo[1,2-a]pyridine Derivatives: An Update

5. Imidazo[1,2-a]pyridines Susceptible to Excited State Intramolecular Proton Transfer: One-Pot Synthesis via an Ortoleva–King Reaction

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