The addition of alkylzinc iodides to 1-(phenoxycarbonyl)pyridinium salts
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference27 articles.
1. A convenient and efficient unsymmetrical ketone synthesis from acid chlorides and alkyl iodides catalyzed by palladium
2. Generation of 2-Carboethoxyethylzinc iodide and 3-carboethoxypropylzinc iodide and their application to the synthesis of γ- and δ-keto esters
3. Arylation and vinylation of 2-carboethoxyethylzinc iodide and 3-carboethoxypropylzinc iodide catalyzed by palladium
4. Regioselective addition of Grignard reagents to 1-acylpyridinium salts. A convenient method for the synthesis of 4-alkyl(aryl)pyridines
5. Regioselective arylation of 3-bromopyridine
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3. A Mild, Functional Group Tolerant Addition of Organozinc Nucleophiles to N-Activated Quinolines and Isoquinolines;The Journal of Organic Chemistry;2017-09-07
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5. Organozinc Chemistry;Organometallics in Synthesis: A Manual;2013-06-26
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