Indium metal and its halides in organic synthesis

Authors
Citation
Bc. Ranu, Indium metal and its halides in organic synthesis, EUR J ORG C, (13), 2000, pp. 2347-2356
Citations number
90
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
ISSN journal
1434193X → ACNP
Issue
13
Year of publication
2000
Pages
2347 - 2356
Database
ISI
SICI code
1434-193X(200007):13<2347:IMAIHI>2.0.ZU;2-Y
Abstract
This review highlights the applications of indium metal and indium(III) hal ides in organic synthesis with particular reference to regio-, stereo-, and chemoselectivity. Indium-mediated reactions include the regioselective all ylation of alkynes, the stereoselective debromination of vic-aryl-substitut ed dibromides, the homocoupling of alkyl/aryl halides, and the reduction of cc-halocarbonyl compounds. Indium trichloride has been used as a Lewis aci d catalyst in epoxide rearrangements, in the synthesis of a-amino phosphona tes, and in the construction of the quinoline system. Indium triiodide has proven to be a very efficient catalyst for transesterification processes.