Synthesis of poly-substituted tetrahydropyridines from Baylis–Hillman adducts modified with N-allylamino group via radical cyclization
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference37 articles.
1. Unusual synthesis of dihydropyrido[2,1-a]isoindolone derivatives by radical cyclization of enamides of Baylis–Hillman adducts
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3. C(8) Substituted 1-Azabicyclo[3.3.1]non-3-enes and C(8) Substituted 1-Azabicyclo[3.3.1]nonan-4-ones: Novel Muscarinic Receptor Antagonists
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2. Effect of Methods and Catalysts on the One-pot Synthesis of Tetrahydropyridine Derivatives: A Mini-Review;Orbital: The Electronic Journal of Chemistry;2021-10-05
3. Tetrahydropyridine: a promising heterocycle for pharmacologically active molecules;TURKISH JOURNAL OF CHEMISTRY;2018-10-11
4. Organocatalytic Synthesis of 4-Aryl-1,2,3,4-tetrahydropyridines from Morita-Baylis-Hillman Carbonates through a One-Pot Three-Component Cyclization;The Journal of Organic Chemistry;2018-01-10
5. 15.1.4 Pyridines (Update 2016);Knowledge Updates 2016/1;2016
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