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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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
Subjects:
2-methyl tetralone and piperidine-D11
ammonium salts
D-enols
deuterium
enolates
internal deuterium transfer
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container_issue 6
container_start_page 359
container_title Journal of labelled compounds & radiopharmaceuticals
container_volume 47
creator Coumbarides, Gregory S.
Eames, Jason
Suggate, Michael J.
description 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.
doi_str_mv 10.1002/jlcr.822
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source Wiley
subjects 2-methyl tetralone and piperidine-D11
ammonium salts
D-enols
deuterium
enolates
internal deuterium transfer
title Investigations into the regioselective C-deuteriation of enolates derived from 2-methyl tetralone using piperidine-d11
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