Reduction of Biginelli compounds by LiAlH4: a rapid access to molecular diversity
Author:
Affiliation:
1. Department of Chemistry
2. Faculty of Science and Mathematics
3. University of Niš
4. Niš
5. Serbia
Abstract
The reduction of Biginelli compounds by LiAlH4 provides a rapid access to molecular diversity.
Funder
Ministry of Education, Science and Technological Development
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2016/RA/C6RA24535H
Reference14 articles.
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2. L. Kurti and B.Czako, Strategic Applications of Named Reactions in Organic Synthesis, Elsevier Academic Press, 1st edn, 2005
3. Recent Advances in the Biginelli Dihydropyrimidine Synthesis. New Tricks from an Old Dog
4. Biologically active dihydropyrimidones of the Biginelli-type — a literature survey
5. A Reexamination of the Mechanism of the Biginelli Dihydropyrimidine Synthesis. Support for an N-Acyliminium Ion Intermediate1
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2. Substitutional effects on the reactivity and thermal stability of dihydropyrimidinones;Journal of Molecular Structure;2021-01
3. Enantioselective N -Acylation of Biginelli Dihydropyrimidines by Oxidative NHC Catalysis;European Journal of Organic Chemistry;2020-04-17
4. Green synthesis and structural characterization of novel N1-substituted 3,4-dihydropyrimidin-2(1H)-ones;Green Processing and Synthesis;2019-01-28
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