Smith, Keith and El-Hiti, Gamal A. 2004. Regioselective control of electrophilic aromatic substitution reactions. Current Organic Synthesis 1 (3) , pp. 253-274. 10.2174/1570179043366747 |
Official URL: http://www.benthamscience.com/contents.php-JCode-C...
Abstract
para-Regioselective electrophilic aromatic substitution reactions, for example nitration, alkylation, acylation, sulfonylation and halogenation, can be achieved by carrying out reactions over solid catalysts such as zeolites, under modest conditions via shape-selectivity. By contrast, organolithium reagents can play an important role when ortho-products are desirable. ortho-Lithiation has been applied for the synthesis of more complex substituted heterocycles that are difficult to prepare by other means.
Item Type: | Article |
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Status: | Published |
Schools: | Chemistry |
Subjects: | Q Science > QD Chemistry |
Uncontrolled Keywords: | regioisomers; zeolites; electrophilic aromatic substitution reactions; directed lithiation; shape selectivity; heterocycles |
Publisher: | Bentham Science |
ISSN: | 1570-1794 |
Last Modified: | 04 Jun 2017 02:51 |
URI: | https://orca.cardiff.ac.uk/id/eprint/12711 |
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