Regiospecific substitution of N-acyl-2,3-dihydro-4-pyridones at C-5 via halogenation and cross-coupling
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference30 articles.
1. Additiom of Grignard reagents to 1-acyl-4-methoxypyridinum salts. An approach to the synthesis of quinolizidinones.
2. Stereoselective addition of (triphenylsilyl)magnesium bromide to chiral 1-acyl-4-methoxypyridinium salts. Synthesis and reactions of enantiopure 1-acyl-2-(triphenylsilyl)-2,3-dihydro-4-pyridones
3. Regio- and Stereoselective Addition of Nucleophiles to 1-Phenoxycarbonyl-2,3-dihydropyridinium Salts
4. Regioselective Substitution in Aromatic Six-Membered Nitrogen Heterocycles
5. Asymmetric synthesis of 2-alkyl(aryl)-2,3-dihydro-4-pyridones by addition of Grignard reagents to chiral 1-acyl-4-methoxypyridinium salts
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