Phosphoric acid-catalyzed asymmetric N-propargylation of pyridazinones and 2-pyridones
Author:
Affiliation:
1. Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering, Changzhou University, Changzhou 213164, China
Abstract
Funder
National Natural Science Foundation of China
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2023/QO/D3QO00995E
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1. Synthesis and biological evaluation of pyridazine derivatives as novel HIV-1 NNRTIs
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3. Discovery of novel 2,6-disubstituted pyridazinone derivatives as acetylcholinesterase inhibitors
4. Structure-Based Design, Synthesis, and Biological Evaluation of Irreversible Human Rhinovirus 3C Protease Inhibitors. 8. Pharmacological Optimization of Orally Bioavailable 2-Pyridone-Containing Peptidomimetics
5. Structure-Based Design, Synthesis, and Biological Evaluation of Irreversible Human Rhinovirus 3C Protease Inhibitors. 6. Structure−Activity Studies of Orally Bioavailable, 2-Pyridone-Containing Peptidomimetics
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