Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Catalytic, green and regioselective friedel-crafts acylation of simple aromatics and heterocycles over zeolites

El-Hiti, Gamal A., Smith, Keith and Hegazy, Amany S. 2015. Catalytic, green and regioselective friedel-crafts acylation of simple aromatics and heterocycles over zeolites. Current Organic Chemistry 19 (7) , pp. 585-598. 10.2174/1385272819666150211002257

Full text not available from this repository.

Abstract

Traditional Friedel-Crafts acylation reactions of aromatics suffer from low regio-selectivity towards para- or more linear isomers and usually require stoichiometric quantities of Lewis acids, which are hydrolysed to produce toxic waste during aqueous work-up. Zeolites can catalyse and enhance the selectivity in Friedel-Crafts acylation reactions of simple aromatics and heterocycles. For example, high regioselectivity was achieved in acylation of aromatic ethers, aromatic hydrocarbons and heterocycles over zeolites. This brief review highlights the importance of zeolites to enhance the regioselectivity in Friedel-Crafts acylation reactions.

Item Type: Article
Status: Published
Schools: Chemistry
Publisher: Bentham Science Publishers
ISSN: 1385-2728
Date of Acceptance: 9 February 2015
Last Modified: 01 Sep 2017 12:02
URI: https://orca.cardiff.ac.uk/id/eprint/102292

Citation Data

Cited 16 times in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item Edit Item