## 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
Pyrrolothieno[1,4]diazepines. Part V. Study of their chemical reactivity and first synthesis of oxazino[4,3-c]pyrrolo[1,2-a]thieno[2,3-f] [1,4]diazepines
β Scribed by Michel Boulouard; Patrick Dallemagne; Sylvain Rault
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1997
- Tongue
- English
- Weight
- 524 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0022-152X
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β¦ Synopsis
Abstract
The study of the chemical reactivity of methyloxopyrrolothienodiazepinones led to new derivatives such as oximes, methyloximes, hydrazones and alcohols and also, according to an intramolecular cyclization, to new oxazino[4,3βc]pyrrolo[1,2βa]thieno[3,2βf][1,4]diazepines.
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
## Abstract The synthetic pathway leading to 5,6βdihydroβ4__H__βfuro[3,2β__f__]pyrrolo[1,2β__a__][1,4]diazepines is described in four steps starting from Ξ±βbromophenones __via__ 2βaminoβ3βfuronitriles.