Direct Aminolysis of Ethoxycarbonylmethyl 1,4-Dihydropyridine-3-carboxylates-Reference-Cited by-同舟云学术

Direct Aminolysis of Ethoxycarbonylmethyl 1,4-Dihydropyridine-3-carboxylates

Published:2015-11-12 Issue:11 Volume:20 Page:20341-20354
ISSN:1420-3049
Container-title:Molecules
language:en
Short-container-title:Molecules

Author:

Vigante Brigita,Rucins Martins,Plotniece Aiva,Pajuste Karlis,Luntena Iveta,Cekavicus Brigita,Bisenieks Egils,Smits Rufus,Duburs Gunars,Sobolev Arkadij

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

Link

http://www.mdpi.com/1420-3049/20/11/19697/pdf

Reference28 articles.

1. The 1,4-Dihydropyridine Nucleus: A Pharmacophoric Template Part 1. Actions at Ion Channels

2. Synthesis and studies of calcium channel blocking and antioxidant activities of novel 4-pyridinium and/or N-propargyl substituted 1,4-dihydropyridine derivatives

3. 1,4-Dihydropyridine Scaffold in Medicinal Chemistry, The Story So Far And Perspectives (Part 2): Action in Other Targets and Antitargets

4. Chemoenzymatic synthesis of enantiopure 1,4-dihydropyridine derivatives

5. Effect of substituents in the dihydropyridine ring on the reactivity of the ester group of 3,5-dialkoxycarbonyl-1,4-dihydropyridines

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