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Non-Conventional Methodologies in the Synthesis of 1-Indanones

1-Indanones have been successfully prepared by means of three different non-conventional techniques, namely microwaves, high-intensity ultrasound and a Q-tube™ reactor. A library of differently substituted 1-indanones has been prepared via one-pot intramolecular Friedel-Crafts acylation and their ef...

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Detalles Bibliográficos
Autores principales: Oliverio, Manuela, Nardi, Monica, Costanzo, Paola, Cariati, Luca, Cravotto, Giancarlo, Giofrè, Salvatore Vincenzo, Procopio, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271961/
https://www.ncbi.nlm.nih.gov/pubmed/24786845
http://dx.doi.org/10.3390/molecules19055599
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author Oliverio, Manuela
Nardi, Monica
Costanzo, Paola
Cariati, Luca
Cravotto, Giancarlo
Giofrè, Salvatore Vincenzo
Procopio, Antonio
author_facet Oliverio, Manuela
Nardi, Monica
Costanzo, Paola
Cariati, Luca
Cravotto, Giancarlo
Giofrè, Salvatore Vincenzo
Procopio, Antonio
author_sort Oliverio, Manuela
collection PubMed
description 1-Indanones have been successfully prepared by means of three different non-conventional techniques, namely microwaves, high-intensity ultrasound and a Q-tube™ reactor. A library of differently substituted 1-indanones has been prepared via one-pot intramolecular Friedel-Crafts acylation and their efficiency and “greenness” have been compared.
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spelling pubmed-62719612018-12-21 Non-Conventional Methodologies in the Synthesis of 1-Indanones Oliverio, Manuela Nardi, Monica Costanzo, Paola Cariati, Luca Cravotto, Giancarlo Giofrè, Salvatore Vincenzo Procopio, Antonio Molecules Article 1-Indanones have been successfully prepared by means of three different non-conventional techniques, namely microwaves, high-intensity ultrasound and a Q-tube™ reactor. A library of differently substituted 1-indanones has been prepared via one-pot intramolecular Friedel-Crafts acylation and their efficiency and “greenness” have been compared. MDPI 2014-04-30 /pmc/articles/PMC6271961/ /pubmed/24786845 http://dx.doi.org/10.3390/molecules19055599 Text en © 2014 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Oliverio, Manuela
Nardi, Monica
Costanzo, Paola
Cariati, Luca
Cravotto, Giancarlo
Giofrè, Salvatore Vincenzo
Procopio, Antonio
Non-Conventional Methodologies in the Synthesis of 1-Indanones
title Non-Conventional Methodologies in the Synthesis of 1-Indanones
title_full Non-Conventional Methodologies in the Synthesis of 1-Indanones
title_fullStr Non-Conventional Methodologies in the Synthesis of 1-Indanones
title_full_unstemmed Non-Conventional Methodologies in the Synthesis of 1-Indanones
title_short Non-Conventional Methodologies in the Synthesis of 1-Indanones
title_sort non-conventional methodologies in the synthesis of 1-indanones
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271961/
https://www.ncbi.nlm.nih.gov/pubmed/24786845
http://dx.doi.org/10.3390/molecules19055599
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