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Open AccessArticle

Non-Conventional Methodologies in the Synthesis of 1-Indanones

1
Dipartimento di Scienze della Salute, Università Magna Graecia, Viale Europa, Germaneto (CZ) 88100, Italy
2
Dipartimento di Chimica, Università della Calabria, Cubo 12C, Arcavacata di Rende (CS) 87036, Italy
3
Dipartimento di Scienza e Tecnologia del Farmaco, Università di Torino, Via Pietro Giuria 9, Torino 10125, Italy
4
Dipartimento Scienza del Farmaco e Prodotti per la salute, Università di Messina, Via Santissima Annunziata, Messina 98168, Italy,
*
Author to whom correspondence should be addressed.
Molecules 2014, 19(5), 5599-5610; https://doi.org/10.3390/molecules19055599
Received: 2 April 2014 / Revised: 19 April 2014 / Accepted: 23 April 2014 / Published: 30 April 2014
(This article belongs to the Section Organic Chemistry)
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. View Full-Text
Keywords: 1-indanones; microwaves; ultrasound; Q-tube™; Friedel-Crafts acylation 1-indanones; microwaves; ultrasound; Q-tube™; Friedel-Crafts acylation
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MDPI and ACS Style

Oliverio, M.; Nardi, M.; Costanzo, P.; Cariati, L.; Cravotto, G.; Giofrè, S.V.; Procopio, A. Non-Conventional Methodologies in the Synthesis of 1-Indanones. Molecules 2014, 19, 5599-5610. https://doi.org/10.3390/molecules19055599

AMA Style

Oliverio M, Nardi M, Costanzo P, Cariati L, Cravotto G, Giofrè SV, Procopio A. Non-Conventional Methodologies in the Synthesis of 1-Indanones. Molecules. 2014; 19(5):5599-5610. https://doi.org/10.3390/molecules19055599

Chicago/Turabian Style

Oliverio, Manuela; Nardi, Monica; Costanzo, Paola; Cariati, Luca; Cravotto, Giancarlo; Giofrè, Salvatore V.; Procopio, Antonio. 2014. "Non-Conventional Methodologies in the Synthesis of 1-Indanones" Molecules 19, no. 5: 5599-5610. https://doi.org/10.3390/molecules19055599

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