ChemInform Abstract: Reactivity of Dimethylphenylsilyllithium Toward 5- and 6-Substituted 1,3-Dimethyluracil Derivatives.
β Scribed by Raffaele Saladino; Luigi Stasi; Gabriele Volpe; Rosario Nicoletti; Maurizio Botta
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 35 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Reactivity of Dimethylphenylsilyllithium Toward 5-and 6-Substituted 1,3-Dimethyluracil Derivatives.
-The reactions of Li-SiMe 2 -Ph (II) with several 5- and6-substituted 1,3-dimethyluracil derivatives is studied. In general, (II) reacts with 5-substituted uracils by selective addition at the electrophilic C-6 position of the uracil ring to furnish the corresponding 6silyl-5,6-dihydrouracil derivatives [cf. (VII)]. Reactions of silyllithium (II) with 6-substituted uracils show a different selectivity and an unusual addition at the 5-position can be observed [cf. (XI)]. -(SALADINO, RAFFAELE; STASI,
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v