Reactions of the N,N-dialkylpyridylcarboxylic amides with lithium amides. Regioselective lithiation of N,N-diisopropylpyridylcarboxylic amides, a useful method for synthesis of 2,3- and 3,4-disubstituted pyridines-Reference-Cited by-同舟云学术

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Reactions of the N,N-dialkylpyridylcarboxylic amides with lithium amides. Regioselective lithiation of N,N-diisopropylpyridylcarboxylic amides, a useful method for synthesis of 2,3- and 3,4-disubstituted pyridines

Published:1980-01 Issue:49 Volume:21 Page:4739-4742
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Epsztajn Jan,Berski Zbigniew,Brzeziński Jacek Z.,Jóźwiak Andrzej

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference10 articles.

1. Oxazolines as activating groups in aromatic substitution. Regioselective metallation of the 3-position in pyridine.

2. Oxazolines as Activating Groups in Aromatic Substitution. Selective Metalation or Addition to the 4-Position of Pyridine. A New Synthesis of 1,4-Dihydropyridines

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1. meta‐Selective C−H Functionalization of Pyridines;Angewandte Chemie International Edition;2023-07-13

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3. Identification of a Novel Neuropeptide S Receptor Antagonist Scaffold Based on the SHA-68 Core;Pharmaceuticals;2021-10-06

4. Directed Lithiation and Substitution of Pyridine Derivatives;HETEROCYCLES;2015

5. Directed lithiation of simple aromatics and heterocycles for synthesis of substituted derivatives;ARKIVOC;2015

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