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Investigations into the regioselective C-deuteriation of enolates derived from 2-methyl tetralone using piperidine-d11

Results are reported on the regioselective C‐deuteriation of 2‐methyl tetralone using piperidine‐d11 as a deuterium source. The results presented further aid the understanding of kinetic deuteriation of amine–enolate complexes. Copyright © 2004 John Wiley & Sons, Ltd.

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Bibliographic Details
Published in:Journal of labelled compounds & radiopharmaceuticals 2004-05, Vol.47 (6), p.359-371
Main Authors: Coumbarides, Gregory S., Eames, Jason, Suggate, Michael J.
Format: Article
Language:English
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Summary:Results are reported on the regioselective C‐deuteriation of 2‐methyl tetralone using piperidine‐d11 as a deuterium source. The results presented further aid the understanding of kinetic deuteriation of amine–enolate complexes. Copyright © 2004 John Wiley & Sons, Ltd.
ISSN:0362-4803
1099-1344
DOI:10.1002/jlcr.822