Palladium-catalyzed C3-selective C–H oxidative carbonylation of imidazo[1,2-a]pyridines with CO and alcohols: a way to access esters-Reference-Cited by-同舟云学术

Palladium-catalyzed C3-selective C–H oxidative carbonylation of imidazo[1,2-a]pyridines with CO and alcohols: a way to access esters

Published:2020 Issue:4 Volume:7 Page:697-701
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Wang Shoucai¹²³⁴⁵,Zhang Siyu¹²³⁴⁵,Liu Meichen¹²³⁴⁵,Zang Jiawang¹²³⁴⁵,Jiang Guangbin¹²³⁴⁵,Ji Fanghua¹²³⁴⁵^ORCID

Affiliation:

1. Guangxi Key Laboratory of Electrochemical and Magnetochemical Function Materials

2. College of Chemistry and Bioengineering

3. Guilin University of Technology

4. Guilin 541004

5. People's Republic of China

Abstract

A palladium-catalyzed C3-selective C–H oxidative carbonylation for the synthesis of various esters from imidazo[1,2-a]pyridines and CO with high efficiency and high atom economy has been developed.

Funder

Natural Science Foundation of Guangxi Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/QO/D0QO00003E

Reference57 articles.

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2. Imidazo[1,2-a]pyridine 1-oxide. Synthesis and chemistry of a novel type of N-oxide

3. Synthesis of Indeno-Fused Derivatives of Quinolizinium Salts, Imidazo[1,2-a]pyridine, Pyrido[1,2-a]indole, and 4H-Quinolizin-4-one via Benzannulated Enyne−Allenes

4. Synthesis of Imidazo[1,2-a]pyridine C-Nucleosides with an Unexpected Site of Ribosylation

5. New and unusual scaffolds in medicinal chemistry

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