ChemInform Abstract: Furan Ring Opening—Pyrrole Ring Closure: A New Route to Pyrrolo[1,2-d][1,4]benzodiazepin-6-ones.
✍ Scribed by Tatyana A. Nevolina; Vitaly A. Shcherbinin; Olga V. Serdyuk; Alexander V. Butin
- Publisher
- John Wiley and Sons
- Year
- 2012
- Weight
- 29 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Abstract
The synthesis of title compounds (V) is based on the catalyzed recyclization of substrates (IV).
📜 SIMILAR VOLUMES
## Abstract A principally new method for the synthesis of polyfunctional title compounds is developed by recyclization of 2‐[2‐(acylamino)benzyl]furans in the presence of POCl~3~.
## 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
A New Entry to [1,2,4]Triazolo [1,5-a][1,4]benzodiazepin-6-ones via Intramolecular Nitrilimine Cycloaddition to the Cyano Group. -A new methodology is presented for the synthesis of title benzodiazepinones (VIII), which are of potential pharmacological interest. Thus, employing nitrilimines, genera