Regioselective Acylation of Heterocyclic Ketene Aminals with Acetyl Chloride. -Acylation of ketene aminals (I) affords exclusively the N-acylated products (IV), while in the presence of triethylamine and Hg(CN)2 the C-acylated products (III) predominate together with (IV) as minor products. The (E)
ChemInform Abstract: Acetyl Ketene Aminals in Nenitzescu Reaction.
β Scribed by L. M. Alekseeva; T. I. Mukhanova; E. K. Panisheva; O. S. Anisimova; K. F. Turchin; A. V. Komkov; V. A. Dorokhov; V. G. Granik
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 30 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
β¦ 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 βFull Textβ option. The original article is trackable via the βReferencesβ option.
π SIMILAR VOLUMES
## 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
Cyclic Enaminoketones in the Nenitzescu Reaction. -The Nenitzescu reaction of cyclic enaminoketone (I) with benzoquinones proceeds via two different directions affording dibenzofuran derivatives (III) and spiro-compounds (IV). The reaction outcome depends obviously on the structure of the enamine e