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Investigations into the regioselective C-deuteriation of enolates using a diisopropylammonium salt

✍ Scribed by Gregory S. Coumbarides; Jason Eames; Neluka Weerasooriya

Publisher
John Wiley and Sons
Year
2002
Tongue
French
Weight
125 KB
Volume
45
Category
Article
ISSN
0022-2135

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✦ Synopsis

Abstract

Results are reported on the regioselective C‐deuteriation of 2‐methyl tetralone using a series of diisopropylamine derived D‐sources. The results presented further aid the understanding of kinetic deuteriation of both ‘base‐containing’ and ‘base‐free’ enolates. Copyright © 2002 John Wiley & Sons, Ltd.

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