Chimie des amino-carbinols hétérocycliques pseudobasiques. Réactions entre dihydro-3,4 isoquinoléines et aminoalcoyl-cétones

Cs Szantay, L. Novák, A. Buzas

Research output: Contribution to journalArticle

Abstract

The reaction between dihydro-3,4-isoquinolines and α-β unsaturated ketones, yields a new type of cyclic system which can be considered as a derivative of pyrido-oxazine. When treated with acids, this derivatives gives quaternary ammonium salts which can either regenerate the initial product or produce a new cyclic system, depending on the pH. These cyclic systems are new.

Original languageFrench
Pages (from-to)4713-4723
Number of pages11
JournalTetrahedron
Volume24
Issue number13
Publication statusPublished - 1968

ASJC Scopus subject areas

  • Drug Discovery
  • Organic Chemistry
  • Biochemistry

Cite this

Chimie des amino-carbinols hétérocycliques pseudobasiques. Réactions entre dihydro-3,4 isoquinoléines et aminoalcoyl-cétones. / Szantay, Cs; Novák, L.; Buzas, A.

In: Tetrahedron, Vol. 24, No. 13, 1968, p. 4713-4723.

Research output: Contribution to journalArticle

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