This submission belongs to the session a. General Organic Synthesis of the event The 4th International Electronic Conference on Synthetic Organic Chemistry
Published date
11 Sep, 2000
Citation
C. Oliver Kappe, Olga Kataeva, Nancy Hecq, Jean Jacques Vanden Eynde, Microwave-mediated Regioselective Synthesis of Novel Pyrimido[1,2-a]pyrimidines under Solvent-free Conditions, in Proceedings of The 4th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2000, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-4-01830
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Microwave-mediated Regioselective Synthesis of Novel Pyrimido[1,2-a]pyrimidines under Solvent-free Conditions
Jean Jacques Vanden Eynde 1
Nancy Hecq 1
Olga Kataeva 2
C. Oliver Kappe 3
1. University of Mons-Hainaut, Organic Chemistry Department, Place du Parc 20, B – 7000 Mons, Belgium
2. A.E. Arbuzov Institute of Organic and Physical Chemistry, Russian Academy of Sciences, Arbuzov street 8, Kazan 420083, Russia
3. Institute of Chemistry, Karl-Franzens-University Graz, Heinrichstrasse 28, A – 8010 Graz, Austria
Abstract
In recent years there has been increasing interest in the design of alkyl 1,4-dihydropyrimidine-5-carboxylates (1,4-DHPMs) and related Biginelli-like compounds [1] which are presented as valuable substitutes [2] for the well known Nifedipine® and other 1,4-dihydropyridine drugs [3] clinically used in the treatment of cardiovascular diseases. That interest is illustrated, i.a., by the disclosure of elegant protocols involving solid phase synthesis approaches [4] as well as solvent-free preparations under microwave irradiation. [5] The purpose of the present work is to extend the scope of those studies to 2-amino derivatives and especially to the evaluation of their synthetic potential for the construction of novel pyrimido[1,2-a]pyrimidines, a ring system that can be found in marine-derived natural products such as crambescidin [6] and batzelladine [7] alkaloids.
Keywords
n/a
Novel Synthesis of a,b-Diketoesters from a,a-Dioxo-type Oximes or Oxime Ethers via Zinc-Induced Deoximation
Synthesis, Resolution and Use in Enantioselective Catalysis of an Axially Chiral Binaphthyl-templated P,S-heterodonor Ligand (binaps)