Azacycloalkanes. XXXVII: 3,4-Dihydro-5H-pyrrolo[1,2-a]-diazepine and Its Conversions
✍ Scribed by A. M. Likhosherstov; V. P. Peresada; V. G. Vinokurov; A. P. Skoldinov
- Publisher
- Springer
- Year
- 2005
- Tongue
- English
- Weight
- 104 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0091-150X
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract The synthetic pathway leading to 5,6‐dihydro‐4__H__‐furo[3,2‐__f__]pyrrolo[1,2‐__a__][1,4]diazepines is described in four steps starting from α‐bromophenones __via__ 2‐amino‐3‐furonitriles.
## Abstract Fused tricyclic 7‐phenyl‐5__H__‐thizolo[5,4‐__e__]pyrrolo[1,2‐__a__][1,4]diazepin‐10(9__H__)one (**10**) was prepared by thermolysis of 2‐phenyl‐4‐(1‐pyrrolylmethyl)thiazole‐5‐carbonyl azide (**9**) in acetic acid. In addition, starting from **10**, 7‐phenyl‐5__H__‐thiazolo [5,4‐__e__][
-The first synthesis of a new type of 1,4-diazepine derivatives, compounds (VIII) and (X), from α-bromophenones (I) via intermediate 2-amino-3-furonitriles is described. -(FENG, XIAO; LANCELOT,