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Mechanism of decarboxylation of 1,3-dimethylorotic acid revisited: Trapping of the reaction intermediate

✍ Scribed by Michael P. Nakanishi; Weiming Wu


Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
124 KB
Volume
39
Category
Article
ISSN
0040-4039

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✦ Synopsis


The deearboxylafion of 1,3-dimethylorotic acid was investigated to study the nature of the reaction intermediate. 6-Benzyl-l,3-dimethyluracil was isolated when the deearboxylation was carried out in benzyl bromide, indicating.the involvement of a carbon-6 centered nucleophilic intermediate in the reaction pathway.


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