Volume 29, Issue 1
Heterocyclic Compounds
Full Access

ChemInform Abstract: Organic Nitrates. Part 2. Synthesis and Biological Activities of 4-Nitrooxymethylphenyl-1,4-dihydropyridines.

J. LEHMANN

J. LEHMANN

Pharm. Inst., Rhein. Friedrich-Wilhelms-Univ., D-53115 Bonn, Germany

Search for more papers by this author
R. KAHLICH

R. KAHLICH

Pharm. Inst., Rhein. Friedrich-Wilhelms-Univ., D-53115 Bonn, Germany

Search for more papers by this author
C. MEYER ZUM GOTTESBERGE

C. MEYER ZUM GOTTESBERGE

Pharm. Inst., Rhein. Friedrich-Wilhelms-Univ., D-53115 Bonn, Germany

Search for more papers by this author
U. FRICKE

U. FRICKE

Pharm. Inst., Rhein. Friedrich-Wilhelms-Univ., D-53115 Bonn, Germany

Search for more papers by this author
First published: 24 June 2010

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

In order to obtain new vascular active substances synthetic procedures for 2-nitrooxymethyl-4-phenyl- and 4-nitrooxymethylphenyl-1,4-dihydropyridines, e.g. (V), are tested. The first ones are not available because of their spontaneous lactonization. The second type (V) is prepared by the Hantzsch reaction and found to be negative inotropic. The vasodilator activity of all derivatives is less than that of nitrendipine.

chemical structure image

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.