Isolation, Synthesis, and Biological Activity of Quindoline, a Valuable Indoloquinoline Natural Product and Useful Key Intermediate
Author:
Affiliation:
1. Instituto de Química Rosario (IQUIR, CONICET-UNR) and Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario (UNR)
Abstract
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry,Catalysis
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0036-1591947.pdf
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3. Efficient Buchwald–Hartwig and nitrene-mediated five-membered ring closure approaches to the total synthesis of quindoline. Unexpected direct conversion of a nitro group into a phosphazene;RSC Advances;2023
4. An efficient approach for 3-haloquinoline synthesis: PhI(OAc)2-mediated A3-X type tandem annulation of amine, aldehyde, alkyne and halide salt;Tetrahedron Letters;2022-07
5. Synthesis of Fluorescent, DNA-Binding Benzo[b]indolonaphthyridinium Derivatives by a Misguided Westphal Condensation;The Journal of Organic Chemistry;2022-03-03
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