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The use of1H NMR for yield determination in the regioselective epoxidation of squalene

✍ Scribed by Hans A. J. Aerts; Bert F. E. Sels; Pierre A. Jacobs


Book ID
107490843
Publisher
Springer-Verlag
Year
2005
Tongue
English
Weight
166 KB
Volume
82
Category
Article
ISSN
0003-021X

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Regioselectivity in the glutathione-phen
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A detailed 360 MHz ' H NMR analysis leads to the unambiguous structural identification of the compound , which is regioselectivelv formed in the chemical and enzymatical reactions between glutathione and phenvlqlycidyl ether. The thiol group attacks preferentially the least substituted oxirane carbo