Catalyst‐Free One‐Pot Synthesis of 2,4,6‐Triaryl‐1,4‐dihydropyridines in Ionic Liquid and Their Catalyzed Activity on Two Simple Diels

Catalyst‐Free One‐Pot Synthesis of 2,4,6‐Triaryl‐1,4‐dihydropyridines in Ionic Liquid and Their Catalyzed Activity on Two Simple Diels–Alder Reactions

Published:2008-02-13 Issue:5 Volume:38 Page:666-673
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Wu Hui¹²,Wan Yu¹²,Lu L. L.³,Shen Yang¹,Ye L.¹,Zhang F. R.¹

Affiliation:

1. a School of Chemistry and Chemical Engineering, Xuzhou Normal University , Xuzhou, Jiangsu, China

2. b Key Laboratory of Biotechnology on Medical Plants of Jiangsu Province , Xuzhou, Jiangsu, China

3. c Department of Chemical and Textile Engineering , Jiangyin Polytechnic College , Jiangyin, Jiangsu, China

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397910701818446

Reference29 articles.

1. The new generation dihydropyridine type calcium blockers, bearing 4-phenyl oxypropanolamine, display α-/β-Adrenoceptor antagonist and long-Acting antihypertensive activities

2. Synthesis and structure–activity analysis of novel dihydropyridine derivatives to overcome multidrug resistance

3. Combinatorial synthesis and screening of a chemical library of 1,4-dihydropyridine calcium channel blockers

4. Newly synthesized dihydropyridine derivatives as modulators of P-Glycoprotein-mediated multidrug resistance

5. Reaction of in situ generated α,β-unsaturated imines with ch-nucleophiles: a novel and efficient synthesis of pyridines.*

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