Diverse Isoquinoline Scaffolds by Ugi/Pomeranz–Fritsch and Ugi/Schlittler–Müller Reactions
Author:
Affiliation:
1. Drug Design, University of Groningen, Deusinglaan 1, 7313 AV Groningen, The Netherlands
2. Faculty of Chemistry, Jagiellonian University, 3 Ingardena Street, 30-060 Krakow, Poland
Funder
Hartstichting
China Scholarship Council
Qatar Foundation
National Institute of General Medical Sciences
KWF Kankerbestrijding
European Lead Factory
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b00778
Reference74 articles.
1. Isoquinoline derivatives as potential acetylcholinesterase inhibitors
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3. In Vitro Antiplasmodial, Antiamoebic, and Cytotoxic Activities of Some Monomeric Isoquinoline Alkaloids
4. NATURAL COMPOUNDS IN DRUG DISCOVERY. BIOLOGICAL ACTIVITY AND NEW TRENDS IN THE CHEMISTRY OF ISOQUINOLINE ALKALOIDS
5. Identification of novel and potent isoquinoline aminooxazole-Based IMPDH inhibitors
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