Specific N-Alkylation of Hydroxypyridines Achieved by a Catalyst- and Base-Free Reaction with Organohalides-Reference-Cited by-同舟云学术

Specific N-Alkylation of Hydroxypyridines Achieved by a Catalyst- and Base-Free Reaction with Organohalides

Published:2018-05-16 Issue:12 Volume:83 Page:6769-6775
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Feng Bin¹,Li Yang¹,Li Huan¹,Zhang Xu²,Xie Huamei¹,Cao Hongen²,Yu Lei²^ORCID,Xu Qing¹²^ORCID

Affiliation:

1. College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, Zhejiang 325035, PR China

2. Institute of Pesticide of School of Chemistry and Chemical Engineering and School of Horticulture and Plant Protection, Yangzhou University, Yangzhou, Jiangsu 225002, PR China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Zhejiang Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b00787

Reference67 articles.

1. Design, Synthesis, and Crystal Structure of Selective 2-Pyridone Tissue Factor VIIa Inhibitors

2. Pyridones as glucokinase activators: Identification of a unique metabolic liability of the 4-sulfonyl-2-pyridone heterocycle

3. An efficient enzymatic preparation of rhinovirus protease inhibitor intermediates

4. Synthesis of 2-pyridones as tissue factor VIIa inhibitors

5. A Pyridone Analogue of Traditional Cannabinoids. A New Class of Selective Ligands for the CB 2 Receptor

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