Transition-metal-free C–H amidation and chlorination: synthesis of N/N′-mono-substituted imidazopyridin-2-ones from N-pyridyl-N-hydroxylamine intermediates-Reference-Cited by-同舟云学术

Transition-metal-free C–H amidation and chlorination: synthesis of N/N′-mono-substituted imidazopyridin-2-ones from N-pyridyl-N-hydroxylamine intermediates

Published:2018 Issue:50 Volume:54 Page:6935-6938
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Lee Katarzyna N.¹²³⁴^ORCID,Spiegowski Dominique N.¹²³⁴^ORCID,Lee Johnny W.¹²³⁴^ORCID,Lim Sanghyun¹²³⁴^ORCID,Zhao Fuhua¹²³⁴,Ngai Ming-Yu¹²³⁴⁵^ORCID

Affiliation:

1. Department of Chemistry

2. State University of New York

3. New York

4. USA

5. Institute of Chemical Biology and Drug Discovery

Abstract

Transition-metal-free C–H amidation and chlorination for the synthesis of N/N′-mono-substituted imidazopyridin-2-ones from versatile N-pyridyl-N-hydroxylamine intermediates at room temperature.

Funder

National Institute of General Medical Sciences

Stony Brook University

National Institutes of Health

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/CC/C8CC02425A

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1. Asymmetric Synthesis of Telcagepant, a CGRP Receptor Antagonist for the Treatment of Migraine

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3. Calcitonin Gene-Related Peptide Receptor Antagonists: New Therapeutic Agents for Migraine

4. Synthesis and analgesic activity of 1,3-dihydro-3-(substituted phenyl)imidazo[4,5-b]pyridin-2-ones and 3-(substituted phenyl)-1,2,3-triazolo[4,5-b]pyridines

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