One-pot, sequential four-component synthesis of novel heterocyclic [3.3.3] propellane derivatives at room temperature

An efficient, one-pot, two-step, four-component reaction for the synthesis of propellane derivatives is described by the condensation reaction between acenaphthenequinone, malono derivatives, primary amines and β-ketoester or β-diketone derivatives in the presence of triethylamine in ethanol at room...

Descripción completa

Detalles Bibliográficos
Autores principales: Beyrati, Maryam, Hasaninejad, Alireza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079859/
https://www.ncbi.nlm.nih.gov/pubmed/35540742
http://dx.doi.org/10.1039/c8ra01648h
_version_ 1784702651153252352
author Beyrati, Maryam
Hasaninejad, Alireza
author_facet Beyrati, Maryam
Hasaninejad, Alireza
author_sort Beyrati, Maryam
collection PubMed
description An efficient, one-pot, two-step, four-component reaction for the synthesis of propellane derivatives is described by the condensation reaction between acenaphthenequinone, malono derivatives, primary amines and β-ketoester or β-diketone derivatives in the presence of triethylamine in ethanol at room temperature. Using this procedure, all the products were obtained in good to excellent yields.
format Online
Article
Text
id pubmed-9079859
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-90798592022-05-09 One-pot, sequential four-component synthesis of novel heterocyclic [3.3.3] propellane derivatives at room temperature Beyrati, Maryam Hasaninejad, Alireza RSC Adv Chemistry An efficient, one-pot, two-step, four-component reaction for the synthesis of propellane derivatives is described by the condensation reaction between acenaphthenequinone, malono derivatives, primary amines and β-ketoester or β-diketone derivatives in the presence of triethylamine in ethanol at room temperature. Using this procedure, all the products were obtained in good to excellent yields. The Royal Society of Chemistry 2018-04-17 /pmc/articles/PMC9079859/ /pubmed/35540742 http://dx.doi.org/10.1039/c8ra01648h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Beyrati, Maryam
Hasaninejad, Alireza
One-pot, sequential four-component synthesis of novel heterocyclic [3.3.3] propellane derivatives at room temperature
title One-pot, sequential four-component synthesis of novel heterocyclic [3.3.3] propellane derivatives at room temperature
title_full One-pot, sequential four-component synthesis of novel heterocyclic [3.3.3] propellane derivatives at room temperature
title_fullStr One-pot, sequential four-component synthesis of novel heterocyclic [3.3.3] propellane derivatives at room temperature
title_full_unstemmed One-pot, sequential four-component synthesis of novel heterocyclic [3.3.3] propellane derivatives at room temperature
title_short One-pot, sequential four-component synthesis of novel heterocyclic [3.3.3] propellane derivatives at room temperature
title_sort one-pot, sequential four-component synthesis of novel heterocyclic [3.3.3] propellane derivatives at room temperature
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079859/
https://www.ncbi.nlm.nih.gov/pubmed/35540742
http://dx.doi.org/10.1039/c8ra01648h
work_keys_str_mv AT beyratimaryam onepotsequentialfourcomponentsynthesisofnovelheterocyclic333propellanederivativesatroomtemperature
AT hasaninejadalireza onepotsequentialfourcomponentsynthesisofnovelheterocyclic333propellanederivativesatroomtemperature

Ejemplares similares