Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/18123
Title: Actions of bisnucleophiles on (E)-3-[3-(2-Hydroxyaryl)-3-oxoprop-1-en-1-yl]chromones: versatile transformations into oxygen-and nitrogen-containing heterocycles
Author: Hassaine, Ridha
Talhi, Oualid
Taibi, Nadia
Almeida Paz, Filipe A.
Bensaid, Okkacha
Bachari, Khaldoun
Silva, Artur M. S.
Keywords: Chromones
α,β-unsaturated carbonyl systems
Michael additions
Bisnucleophiles
X-ray diffraction
Heterocycles
2D NMR
Issue Date: 2016
Publisher: Georg Thieme Verlag
Abstract: The transformations of (E)-3-[3-(2-hydroxyaryl)-3-oxoprop- 1-en-1-yl]chromones in the presence of methylhydrazine and aromatic bisnucleophiles are described. The reactions generally lead to chromone ring transformation via pyrone ring-opening and heterocyclization to give novel diazoles and (Z)-3-aminomethylenechromanones, respectively. Piperazine catalyzes chromanone ring closure of the starting substrate to afford chromone–chromanone dyads.
Peer review: yes
URI: http://hdl.handle.net/10773/18123
DOI: 10.1055/s-0035-1560829
ISSN: 0936-5214
Appears in Collections:CICECO - Artigos



FacebookTwitterLinkedIn
Formato BibTex MendeleyEndnote Degois 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.