A new approach to the dibenz [b,f] azepine and [b,f] oxepine system
โ Scribed by Ernst D. Bergmann; I. Shahak; Z. Aisenshtat
- Publisher
- Elsevier Science
- Year
- 1968
- Tongue
- French
- Weight
- 110 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0040-4039
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๐ SIMILAR VOLUMES
Reactions of 5-carboxamido-5H-dibenz[bflazepines (la-ld) with glyoxylic acid methylester methyl hemiacetal (GMHA) led to 5-(carboxamido-N-a-hydroxy-acetic acid methyl ester)-5Hdibenz[b,Aazepines (2a-2d). The reactions with glycols yielded the oligoethylene glycol derivatives (3,4). The new compounds
## Abstract Two new antimycobacterial dibenzo[__b__,__f__]oxepins, bauhinoxepins A (=3,3,5โtrimethylbenzo[__b__]pyrano[__g__][1]benzoxepinโ6,11โdiol; **1**) and B (=6โmethoxyโ7โmethylโ2โ(3โmethylbutโ2โenyl)dibenzo[__b__,__f__]oxepineโ1,8โdiol; **2**), were isolated from the roots of __Bauhinia sacc
Synthesis of an Antioxidant Having a Dibenz[b,f ]oxepine Skeleton. -The synthetic title compound (VI) reveals significant difference with the physicochemical data of the natural product, indicating that the original structure has to be revised. Interestingly, the antioxidative activity of synthetic