Brown, D. M. ; Todd, Alexander ; Varadarajan, S. (1956) The structures of some acylcytosines Journal of the Chemical Society, 1956 . pp. 2384-2387. ISSN 0368-1769
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Official URL: http://pubs.rsc.org/en/Content/ArticleLanding/1956...
Related URL: http://dx.doi.org/10.1039/JR9560002384
Abstract
A number of new acyl derivatives of cytosine and 3-methylcytosines are described. Acylation normally yields N4- monoacyl compounds which, in hot 80% acetic acid, yield large amounts of uracil derivatives. Exceptionally, benzoyl chloride can also yield a 1 : N4- dibenzoate from 3-methylcytosine and a tribenzoate from cytosine. Similarly, benzoylation of cytidine yields, according to conditions, either a tetrabenzoyl or pentabenzoyl derivative.
Item Type: | Article |
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Source: | Copyright of this article belongs to Royal Society of Chemistry. |
ID Code: | 70552 |
Deposited On: | 17 Nov 2011 09:39 |
Last Modified: | 17 Nov 2011 09:39 |
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