Split personality of lithium chloride : recent salt effects in organometallic recipes

Hevia, Eva and Mulvey, Robert E. (2011) Split personality of lithium chloride : recent salt effects in organometallic recipes. Angewandte Chemie, 50 (29). pp. 6448-6450. ISSN 0044-8249

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Official URL: https://doi.org/10.1002/anie.201102054

Abstract

Jekyll and Hyde: Pinches of LiCl can catalyze orthometalations of halogen-substituted arenes and addition reactions of unsaturated esters, mediated by lithium diisopropylamide. Larger salt portions can transform weak organometallic bases (e.g., Grignard reagents, zincates) into “turbo” reagents of high reactivity and functional group tolerance. But the presence of LiCl, especially as an overlooked metathesis by-product can be detrimental to other catalytic reactions.

Creators(s):	Hevia, Eva ORCID: https://orcid.org/0000-0002-3998-7506 and Mulvey, Robert E. ORCID: https://orcid.org/0000-0002-1015-2564;
Item type:	Article
ID code:	34744
Keywords:	amides, lithium chloride, metalation, organolithium, salt effect, grignard-reagents, diisopropylamide, bases, catalysis, autocatalysis, heteroarenes, zincation, arenes, zinc, aryl, Chemistry, Medicine(all)
Subjects:	Science > Chemistry
Department:	Faculty of Science > Pure and Applied Chemistry
Depositing user:	Pure Administrator
Date deposited:	14 Nov 2011 14:04
Last modified:	31 Mar 2020 00:57
Related URLs:	Scopus publication
URI:	https://strathprints.strath.ac.uk/id/eprint/34744
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