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Solution structures of chiral lithium amides with internal sulfide coordination: sulfide versus ether coordination in chiral lithium amides
University of Gothenburg.
University of Gothenburg.
University of Gothenburg.
University of Gothenburg.
2004 (English)In: Tetrahedron-Asymmetry, Vol. 15, no 2, 267-274 p.Article in journal (Refereed) Published
Abstract [en]

A series of chiral lithium amides with chelating sulfide groups has been investigated by NMR spectroscopy. These chiral lithium amides have previously been found to mediate higher enantioselectivity in the asymmetric addition of alkyllithium reagents to aldehydes than the corresponding lithium amides containing ether groups. The chiral lithium amido sulfide chelates form homodimers in both diethyl ether and tetrahydrofuran. In diethyl ether both sulfur atoms coordinate to the same lithium while the other lithium in the dimer is solvent coordinated. Tetrahydrofuran favours equivalently solvated homodimers. Mixed dimeric complexes are formed with excess n-butyllithium in both diethyl ether and tetra hydrofuran. The structural information was obtained from observed Li-6,N-15 couplings and cross peaks in the Li-6,H-1 HOESY spectrum. DFT calculations at B3LYP/6-31G(d) level of theory indicate that the Li-S chelate is much less stable than the Li-O chelate. However the calculations indicate that the stability of the dimeric chelates are in agreement with the NMR results of the diethyl ether and tetrahydrofuran solutions. (C) 2003 Elsevier Ltd. All rights reserved.

Place, publisher, year, edition, pages
2004. Vol. 15, no 2, 267-274 p.
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URN: urn:nbn:se:uu:diva-137512DOI: 10.1016/j.tetasy.2003.11.009OAI: oai:DiVA.org:uu-137512DiVA: diva2:378397
Note
internal-pdf://Li-S-coordination-2135180032/Li-S-coordination.pdfAvailable from: 2010-12-15 Created: 2010-12-15 Last updated: 2011-01-07

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