Synthesis of a Library of 5,6-Unsubstituted 1,4-Dihydropyridines Based on a One-Pot 4CR/Elimination Process and Their Application to the Generation of Structurally Diverse Fused Nitrogen Heterocycles
Author:
Affiliation:
1. Departamento de Química Orgánica y Farmacéutica, Facultad de Farmacia, Universidad Complutense, 28040 Madrid, Spain
Publisher
American Chemical Society (ACS)
Subject
General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/cc100084b
Reference113 articles.
1. For selected reviews of diversity-oriented synthesis and its impact in the discovery of bioactive compounds, see:
2. Target-Oriented and Diversity-Oriented Organic Synthesis in Drug Discovery
3. Diversity-oriented synthesis; a challenge for synthetic chemistsElectronic supplementary information (ESI) available: Excel file of all the FDA new molecular entities between the years 1998 and July 2003, and new drug approvals between the years 1990 and 2002. See http://www.rsc.org/suppdata/ob/b3/b310752n/
4. Generating Diverse Skeletons of Small Molecules Combinatorially
5. A Planning Strategy for Diversity-Oriented Synthesis
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