Rates of competing fluoride elimination and iodination from a thiamin-derived Breslow intermediate
Author:
Funder
Natural Sciences and Engineering Research Council of Canada
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry
Reference29 articles.
1. Acyl anion synthons: benzotriazole stabilized compared to classical;Katritzky;ARKIVOC,2006
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3. Structures and reactivities of O-methylated Breslow intermediates;Maji;Angew. Chem. Int. Ed.,2012
4. On the mechanism of thiamine action. VI.1 2-acetylthiazolium salts as “active acetate”;Breslow;J. Am. Chem. Soc.,1960
5. On the mechanism of thiamine action. IV.1 Evidence from studies on model systems;Breslow;J. Am. Chem. Soc.,1958
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