Singh, Ravi P. ; Kamble, Rajesh M. ; Chandra, Kusum L. ; Saravanan, P. ; Singh, Vinod K. (2001) An efficient method for aromatic Friedel–Crafts alkylation, acylation, benzoylation, and sulfonylation reactions Tetrahedron, 57 (1). pp. 241-247. ISSN 0040-4020
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/S0040-4020(00)01005-X
Abstract
Aromatic electrophilic substitution reactions such as alkylation, acylation, benzoylation, and sulfonylation were studied in the presence of a catalytic amount of Cu(OTf)2 and Sn(OTf)2. Cu(OTf)2 was very efficient for alkylation, acylation, and benzoylation reactions. However, in case of sulfonylation reactions, Sn(OTf)2 gave better results.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Aromatic Friedel-Crafts Alkylation; Acylation; Benzoylation; Sulfonylation Reactions; Copper(II)trifluoromethanesulfonate; Tin(II)trifluoromethanesulfonate |
| ID Code: | 55319 |
| Deposited On: | 18 Aug 2011 08:35 |
| Last Modified: | 18 Aug 2011 08:35 |
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