Indium metal and its halides in organic synthesis

Ranu, Brindaban C. (2000) Indium metal and its halides in organic synthesis European Journal of Organic Chemistry, 2000 (13). pp. 2347-2356. ISSN 1434-193X

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Official URL: http://onlinelibrary.wiley.com/doi/10.1002/1099-06...

Related URL: http://dx.doi.org/10.1002/1099-0690(200007)2000:13<2347::AID-EJOC2347>3.0.CO;2-X

Abstract

This review highlights the applications of indium metal and indium(III) halides in organic synthesis with particular reference to regio-, stereo-, and chemoselectivity. Indium-mediated reactions include the regioselective allylation of alkynes, the stereoselective debromination of vic-aryl-substituted dibromides, the homocoupling of alkyl/aryl halides, and the reduction of α-halocarbonyl compounds. Indium trichloride has been used as a Lewis acid catalyst in epoxide rearrangements, in the synthesis of α-amino phosphonates, and in the construction of the quinoline system. Indium triiodide has proven to be a very efficient catalyst for transesterification processes.

Item Type:Article
Source:Copyright of this article belongs to John Wiley and Sons.
Keywords:Indium; Halides; Catalysts; Organic Synthesis
ID Code:41468
Deposited On:30 May 2011 05:12
Last Modified:30 May 2011 05:12

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