Optimized NMR spectroscopic method for the configurational analysis of chemically equivalent vicinal protons

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  • Technical University of Munich (TUM)
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Translated title of the contributionEine Hochdurchsatz-Screeningmethode zur Bestimmung der Syntheseaktivität von Hydrolasen
Original languageEnglish
Pages (from-to)1300-1302
Number of pages3
JournalAngewandte Chemie
Volume42
Issue number11
Publication statusPublished - 13 Mar 2003

Abstract

Differentiating the identical: The measurement of homonuclear coupling constants of spins with identical chemical shifts (as observed in 1,2-disubstituted ethenes) provides important structural information, but its experimental realization is not trivial. A new method results in high sensitivity and simple spectra (see picture) that are easy to interpret. The underlying principle of this method is not limited to symmetric molecules with equivalent spins, but can also be applied to olefinic protons that have similar resonance frequencies.

Keywords

    Alkenes, Configurational analysis, NMR spectroscopy, Spin - spin coupling, Symmetry

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Cite this

Optimized NMR spectroscopic method for the configurational analysis of chemically equivalent vicinal protons. / Luy, Burkhard; Hauser, Gerd; Kirschning, Andreas et al.
In: Angewandte Chemie , Vol. 42, No. 11, 13.03.2003, p. 1300-1302.

Research output: Contribution to journalArticleResearchpeer review

Luy B, Hauser G, Kirschning A, Glaser SJ. Optimized NMR spectroscopic method for the configurational analysis of chemically equivalent vicinal protons. Angewandte Chemie . 2003 Mar 13;42(11):1300-1302. doi: 10.1002/anie.200390335, 10.1002/ange.200390335
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