Phosphorylated enaminones can be obtained by the reaction of enaminone dianions with diphenylphosphinoyl chloride. In most cases, the reaction gave a mixture of monosubstituted and disubstituted compounds. Disubstituted compounds show an interesting NMR spectrum. In fact, the methine proton appears
ChemInform Abstract: Dianions of Acyclic β-Enamino Ketones and Electrophiles. Part 9. Synthesis and Reactivity of Phosphorylated Enaminones.
✍ Scribed by Renato Dalpozzo; Antonio De Nino; Daniela Miele; Antonio Procopio; Antonio Tagarelli; Giuseppe Bartoli
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
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 “Full Text” option. The original article is trackable via the “References” option.
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Reaction of 1-Substituted 2,2-Difluorostyrene with Dianions of β-Enamino Ketones. -The title reaction provides monosubstituted products (III) and pyridinone derivatives (IV) in ratios depending on the type of the .
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v