Synthesis of 1,4-Dihydropyridines by Regioselective Additions of Benzylic Zinc Bromides to Pyridinium Salts and Their Aromatizations to 4-Benzylpyridines-Reference-Cited by-同舟云学术

Synthesis of 1,4-Dihydropyridines by Regioselective Additions of Benzylic Zinc Bromides to Pyridinium Salts and Their Aromatizations to 4-Benzylpyridines

Published:1997-03 Issue:5 Volume:27 Page:781-794
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Krapcho A. Paul,Waterhouse David J.,Hammach Abdelhakim,Di Domenico Roberto,Menta Ernesto,Oliva Ambrogio,Spinelli Silvano

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/00397919708004198

Reference35 articles.

1. Regioselective Substitution in Aromatic Six-Membered Nitrogen Heterocycles

2. Recent advances in the chemistry of dihydropyridines

3. Reactions of 1,4-Dihydropyridines

4. Reaction of Cuprate Reagents with Pyridine in the Presence of Chloroformate. A Novel Synthesis of 1,4-Dihydropyridine Derivatives

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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