Ferric(III) chloride-promoted efficient thiocyanation of arylalkenes: a facile synthesis of dithiocyanates

Yadav, J. S. ; Reddy, B. V. S. ; Gupta, Manoj Kumar (2004) Ferric(III) chloride-promoted efficient thiocyanation of arylalkenes: a facile synthesis of dithiocyanates Synthesis, 2004 (12). pp. 1983-1986. ISSN 0039-7881

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Official URL: https://www.thieme-connect.com/ejournals/abstract/...

Related URL: http://dx.doi.org/10.1055/s-2004-829150

Abstract

Anhydrous FeCl3 oxidizes potassium thiocyanate to the corresponding radical and promotes subsequent addition to nucleophilic olefins to produce dithiocyanate derivatives under mild conditions with high efficiency. Excellent yields and chemoselectivities together with the environmental-friendly nature of the Fe(III) chloride makes this method an attractive alternative to established methods. The use of ferric chloride makes it quite simple, more convenient and practical. This new method offers several advantages such as high conversions, cleaner reaction profiles, short reaction times, and the use of inexpensive and readily available catalyst.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers.
Keywords:Oxidative Radical Addition; Alkenes; Dithiocyanates
ID Code:63233
Deposited On:28 Sep 2011 03:22
Last Modified:28 Sep 2011 03:22

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