Ring transformations of 5-nitropyrimidine via inverse Diels-Alder reactions

Authors :: Valery N. Charushin
Henk C. van der Plas
Source :: Tetrahedron Letters 23 (1982), Tetrahedron Letters, 23, 3965-3968
Publication Year :: 1982
Abstract: 5-Nitropyrimidine undergoes inverse Diels-Alder cycloadditions with ketene_N,N-, -O,O- acetals and enamines resulting in pyridine derivatives. The 1H NMR evidence for the 1 -N,N-diethyl-aminopropyne cycloadduct formation is presented.

Subjects :: Organic Chemistry
Inverse
Ketene
Ring (chemistry)
Biochemistry
Organische Chemie
chemistry.chemical_compound
chemistry
Computational chemistry
Drug Discovery
Pyridine
Diels alder
Proton NMR
Life Science

Language :: English
ISSN :: 00404039
Database :: OpenAIRE
Journal :: Tetrahedron Letters 23 (1982), Tetrahedron Letters, 23, 3965-3968
Accession number :: edsair.doi.dedup.....62811c0307f8ec9213c42d40e0ad1beb

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