## Abstract A high‐yield synthesis of 1‐triphenylmethyl‐3‐__tert__‐butylaziridinone (**4**), its physical and spectral properties, the limits of its thermal stability, and reactions with methanol, benzylamine and sodium methoxide in methanol are described.
ChemInform Abstract: About 1-Triphenylmethyl-3-tert-butylaziridinone and Some of Its Reactions.
✍ Scribed by Istvan Lengyel; Victor Cesare; Halina Karram; Tony Taldone
- Book ID
- 101921363
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 29 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Abstract
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📜 SIMILAR VOLUMES
Reactivity of 1,3-Di-tert-butylaziridinones with Phenyl Substituents. A New Fragmentation of α-Lactams. -Dehydrohalogenation of N-alkyl-α-haloamides (I) with KOH/18-crown-6 provides the aziridinones (II) with bulky substituents. Their decomposition in refluxing methanol gives the expected amides. H
## 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 v