2,4-Disubstituted 1-benzoyl-2,3-dihydro-1H-1,5-benzodiazepines were oxidized by m-chloroperbenzoic acid (MCPBA) to produce 1a, 3-disubstituted 4-benzoyl-1a,2,3,4-tetrahydro-oxazirino[2,3a][1,5]benzodiazepines, a novel tricyclic heterocyclic system. However, 2,4-disubstituted 2,3-dihydro-1H-1,5-benzo
ChemInform Abstract: Synthesis of Oxazirino[2,3-a][1,5]benzodiazepines by Oxidation of 1H-1,5-Benzodiazepines with m-Chloroperbenzoic Acid (MCPBA).
β Scribed by Jiaxi Xu; Liangbi Chen
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0931-7597
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β¦ Synopsis
Abstract
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## 12 -132 2,3-Dihydro-1H-1,5-benzodiazepines: A Conversion of Thiolactams to Amidines. -Benzodiazepinone derivatives (I) are transformed into the corresponding thiolactams (II), which can be converted to a new series of diversely substituted amidines [cf. (IV), (V)]. Ammonia, primary amines and h
## 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 βFull Textβ option. The original article is trackable v