Heterocycles [h]-fused onto 4-oxoquinoline-3-carboxylic acid, Part VI [1]. Synthesis and X-ray structure of model indolo[3,2-b]- and [2,3-b]pyrido[2,3-f]quinoxaline-3-carboxylic esters-Reference-Cited by-同舟云学术

Heterocycles [h]-fused onto 4-oxoquinoline-3-carboxylic acid, Part VI [1]. Synthesis and X-ray structure of model indolo[3,2-b]- and [2,3-b]pyrido[2,3-f]quinoxaline-3-carboxylic esters

Published:2008-06-19 Issue:9 Volume:139 Page:1061-1066
ISSN:0026-9247
Container-title:Monatshefte für Chemie - Chemical Monthly
language:en
Short-container-title:Monatsh Chem

Author:

Abu-Sheaib Esráa S.,Zahra Jalal A.,El-Abadelah Mustafa M.,Boese Roland

Publisher

Springer Science and Business Media LLC

Subject

General Chemistry

Link

http://link.springer.com/content/pdf/10.1007/s00706-008-0883-7.pdf

Reference34 articles.

1. Heterocycles [h]-Fused onto 4-Oxoquinoline-3-carboxylic Acid, V [1]. Synthesis and Antibacterial Activity of Some New 2,3-Disubstituted 7-Oxo-7,10-dihydropyrido[2,3-f]quinoxaline-8-carboxylic Acids and Esters

2. The interaction of ellipticine derivatives with nucleic acids studied by optical and1H-nmr spectroscopy: Effect of size of the heterocyclic ring system

3. Interactions of the antiviral quinoxaline derivative 9-OH-B220 {2,3-dimethyl-6-(dimethylaminoethyl)-9-hydroxy-6H-indolo-[2,3-b]quinoxaline} with duplex and triplex forms of synthetic DNA and RNA

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