Rearrangement Reactions for the Synthesis of Some Oxa- and Aza-tricyclic Rings Heterocyclic Compounds

Authors

  • Mercédesz Tőrincsi
    Affiliation
    Budapest University of Technology and Economics
  • Gábor Hornyánszky
    Affiliation
    Budapest University of Technology and Economics
  • Pál Kolonits
    Affiliation
    Budapest University of Technology and Economics
  • Lajos Novák
    Affiliation
    Budapest University of Technology and Economics
https://doi.org/10.3311/PPch.7290

Abstract

This review article describes the main results of our research during the last 5-6 years. A series of new rearrangement reactions was discovered and used for the synthesis of novel heterocyclic compounds: furo[2,3-f]isoquinolines, furo[3,2 -f]
quinolines, benzo[c]xanthene, benzo[h]chromene, benzo[a]xanthene,  benzo[f]chromene, furo[2,3-f]isoquinoline, spirofuro[3,2-f]quinoline,  cycloalkanoindoles, and benzotriazines.

Keywords:

Claisen rearrangements, aza-Claisen rearrangements, Alderene reaction, furo[2, 3-f]isoquinolines, furo[3, 2-f]quinolones, 2-h]quinolones, cycloalkano[b]indole, benzotriazoles, UV-filters

Citation data from Crossref and Scopus

Crossref
Scopus
Google Scholar
Europe PMC

Published Online

2015-01-21

How to Cite

Tőrincsi, M., Hornyánszky, G., Kolonits, P., Novák, L. “Rearrangement Reactions for the Synthesis of Some Oxa- and Aza-tricyclic Rings Heterocyclic Compounds”, Periodica Polytechnica Chemical Engineering, 59(1), pp. 16–25, 2015. https://doi.org/10.3311/PPch.7290

Issue

Vol. 59 No. 1 (2015)

Section

Articles