Synthesis of imidazo[1,5-a]pyridines via I2-mediated sp3 C–H amination-Reference-Cited by-同舟云学术

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Synthesis of imidazo[1,5-a]pyridines via I2-mediated sp3 C–H amination

Published:2018 Issue:31 Volume:16 Page:5653-5660
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Hu Zhiyuan¹²³⁴,Hou Jiao¹²³⁴,Liu Jie¹²³⁴,Yu Wenquan¹²³⁴^ORCID,Chang Junbiao¹²³⁴

Affiliation:

1. College of Chemistry and Molecular Engineering

2. Zhengzhou University

3. Zhengzhou

4. China

Abstract

A transition-metal-free sp³ C–H amination reaction has been developed employing molecular iodine for imidazo[1,5-a]pyridine synthesis.

Funder

National Natural Science Foundation of China

Zhengzhou University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB01501E

Reference46 articles.

1. Recent advances in the transition metal-catalyzed twofold oxidative C–H bond activation strategy for C–C and C–N bond formation

2. Catalytic C–H amination: recent progress and future directions

3. Catalytic Methods for Aromatic C–H Amination: An Ideal Strategy for Nitrogen-Based Functional Molecules

4. Transition Metal-Catalyzed C–H Amination: Scope, Mechanism, and Applications

5. Recent Trends in Copper-Catalyzed C−H Amination Routes to Biologically Important Nitrogen Scaffolds

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