Reaction of 1-methyluracil with phenylbenzhydrazonoyl chloride Научная публикация
| Журнал |
Chemistry of Heterocyclic Compounds
ISSN: 1573-8353 , E-ISSN: 0009-3122 |
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| Вых. Данные | Год: 1986, Том: 22, Номер: 5, Страницы: 532-538 Страниц : 7 DOI: 10.1007/bf00519534 | ||
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Реферат:
The ambident anion of 1-methyluracil gives with phenylbenzyhydrazonoyl chloride, depending on the conditions, the N-acylation product (polar solvent, room temperature), or the O-acylation product (nonpolar solvent, heating), which rearranges to a cytosine derivative. Convenient methods have been developed for the preparation of 6-methyl-1,3-diphenyl-5,6-dihydro-5-oxopyrimido[4,3-c]triazolium chloride, a fluorescent derivative of 1-methyluracil, from the N-acylation product, and for the rapid base cleavage of the uracil ring under very mild conditions.
Библиографическая ссылка:
Chernyshova N.B.
, Shibaev V.N.
Reaction of 1-methyluracil with phenylbenzhydrazonoyl chloride
Chemistry of Heterocyclic Compounds. 1986. V.22. N5. P.532-538. DOI: 10.1007/bf00519534 Scopus OpenAlex
Reaction of 1-methyluracil with phenylbenzhydrazonoyl chloride
Chemistry of Heterocyclic Compounds. 1986. V.22. N5. P.532-538. DOI: 10.1007/bf00519534 Scopus OpenAlex
Идентификаторы БД:
| Scopus: | 2-s2.0-34250124494 |
| OpenAlex: | W2952454263 |
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