Acetals of lactams and acid amides. 34. Synthesis and properties of enamines of the isoquinoline series

Autor:	N. P. Solov'eva, V. F. Knyazeva, O. S. Anisimova, V. G. Granik, R. G. Glushkov
Rok vydání:	1981
Předmět:	chemistry.chemical_classification chemistry.chemical_compound Sodium ethoxide chemistry Transamination Organic Chemistry Hydrazine Acetal Dimethylformamide Organic chemistry Dehydrogenation Ether Isoquinoline
Zdroj:	Chemistry of Heterocyclic Compounds. 17:370-374
ISSN:	1573-8353 0009-3122
Popis:	The reactions of 1,2,3,4-tetrahydro-3-isoquinolone derivatives with dimethylformamide acetal and the hydrolysis and transamination of the resulting enamino amides — 1,2,3,4-tetrahydro-4-dimethylaminomethylene-3-isoquinolone derivatives — were studied. It is shown that 1,2,3,4-tetrahydro-1-phenyl-6,7-dimethoxy-3-isoquinolone can be converted to the corresponding lactim ether. The reactions of the latter with dimethylformamide acetal and hydrazine and the dehydrogenation of this lactim ether in the presence of sodium ethoxide were studied.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::36c6d3e2a79a80546ee4f7a72a3b4f6f https://doi.org/10.1007/bf00503340 Zobrazit plný text záznamu Full text from SpringerLink