Synthesis of 3-aryl-5,6,7,8-tetrahydro-2-benzopyrilium salts and corresponding isoquinolines

Autor:	G. N. Dorofeenko, G. P. Safaryan
Rok vydání:	1970
Předmět:	chemistry.chemical_classification chemistry.chemical_compound Ketone chemistry Aryl Organic Chemistry Anhydrous medicine Organic chemistry Ether Chloride medicine.drug
Zdroj:	Chemistry of Heterocyclic Compounds. 6:538-540
ISSN:	1573-8353 0009-3122
DOI:	10.1007/bf00500665
Popis:	β,γ-Unsaturated ketones (such as cyclohexylideneacetophenone) are formylated with dichloromethyl butyl ether in the presence of anhydrous aluminum chloride. A method has been developed for the synthesis of 3-aryl-substituted 5,6,7,8-tetrahydro-2-benzopyrilium salts unsubstituted in 1 position. The thus-synthesized salts are converted into the corresponding 5,6,7,8-tetrahydroisoquinolines.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::cdee02339f23cfea13a5982b5e66be5d https://doi.org/10.1007/bf00500665 Zobrazit plný text záznamu Full text from SpringerLink