Highly regio- and chemo-selective γ-addition of benzylic group to N-alkoxycarbonylpyridiniuin salts by means of organotin reagent
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. Reaction of Cuprate Reagents with Pyridine in the Presence of Chloroformate. A Novel Synthesis of 1,4-Dihydropyridine Derivatives
2. Regioselective synthesis of 4-alkylpyridines via 1,4-dihydropyridine derivatives from pyridine
3. Facile synthesis of 4-substituted pyridines using grignard reagents
4. A Convenient Method for the Regioselective Synthesis of 4-Alkyl(aryl)pyridines Using Pyridinium Salts
5. Regioselective addition of Grignard reagents to 1-acylpyridinium salts. A convenient method for the synthesis of 4-alkyl(aryl)pyridines
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1. Pyridinium salts: from synthesis to reactivity and applications;Organic Chemistry Frontiers;2018
2. Synthesis of Pyridine and Dihydropyridine Derivatives by Regio- and Stereoselective Addition toN-Activated Pyridines;Chemical Reviews;2012-02-21
3. Reissert-like Alkenylation of Azaaromatic Compounds with Alkenylzirconocene Chloride Complexes;HETEROCYCLES;2012
4. Copper-Catalyzed Multicomponent Coupling of Organoindium Reagents with Nitrogen-Containing Aromatic Heterocycles;European Journal of Organic Chemistry;2010-05-14
5. Regioselective addition of organomagnesium reagents to N-silyl activated nicotinic acid esters—a convenient method for the synthesis of 4,4-disubstituted 1,4-dihydronicotinates;Tetrahedron;2009-07
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